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Areas of application are the life sciences: biology, biochemistry, biotechnology, medicine and medical technology. The biomarkers are selected from a first group consisting of Amy 1, Apo Al, Carbx, Casp, AFP, ApoM, SAP, Fib-a, Fib-b, Fib-g, ApoE, A2MG, A2MG isoform, Serpin, Clusterin, MHC-fB, SAP isoform, or from a second group consisting of Gpx3, properidin, MUP1, HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C, wherein the biomarkers are regulated by EGF overexpression in a subject.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"}]},"abstract_lang":["en"],"has_abstract":true,"claim":{"en":[{"text":"A biomarker selected from a first group consisting of Amy 1, Apo Al, Carbx, Casp, AFP, ApoM, SAP, Fib-a, Fib-b, Fib-g, ApoE, A2MG, A2MG isoform, Serpin, Clusterin, MHC-fB, SAP isoform, or from a second group consisting of Gpx3, properidin, MUP1, HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C, \nwherein the biomarker is regulated by EGF overexpression in a subject.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"Biomarker as claimed in claim 1 selected from a first group consisting of Amy 1, Apo Al, Carbx, Casp, Fib-a, Fib-b, Fib-g, Clusterin, MHC-fB, SAP isoform or from a second group consisting of HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"Biomarker as claimed in claim 1 selected from a first group consisting of AFP, ApoE, ApoM, or from a second group consisting of Gpx3, A2MG, A2MG isoform, SAP.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"A composition for qualifying the EGFR kinase activity in a subject suffering from or being susceptible to cancer, in particular by an in vitro body fluid analysis, comprising an effective amount of at least one biomarker selected from the first group according to one of the claims 1-3 or an effective amount of at least one biomarker selected from the second group according to one of the claims 1-3.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"Composition as claimed in claim 4 comprising an effective amount of at least one biomarker selected from the first group according to one of the claims 1-3 and an effective amount of at least one biomarker selected from the second group according to one of the claims 1-3.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"Use of a composition as claimed in one of the claims 4-5 for the production of a diagnostic agent, in particular of a diagnostic standard for body fluid analysis.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"Use as claimed in claim 6 for the production of a diagnostic agent for qualifying the EGFR kinase activity in a subject suffering from or being susceptible to cancer, in particular cancer of the liver, lung, breast, colon, prostate, bladder, head and neck, ovary or brain.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"Use as claimed in one of the claims 6-7 for the production of a diagnostic agent for predicting or monitoring the response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"A kit for qualifying the EGFR kinase activity in a subject suffering from or being susceptible to cancer, in particular for predicting or monitoring the response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator, comprising at least one standard (1) indicative of the body fluid level of a biomarker selected from the first group according to one of the claims 1-3 in normal individuals or individuals having cancer associated with increased EGFR kinase activity and/or at least one standard (2) indicative of the body fluid level of a biomarker selected from the second group according to one of the claims 1-3 in normal individuals or individuals having cancer associated with increased EGFR kinase activity, and instructions for the use of the kit.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The kit as claimed in claim 9, wherein the at least one standard (1) comprises an indicative amount of at least one biomarker selected from the first group according to one of the claims 1-3 and/or wherein the at least one standard (2) comprises an indicative amount of at least one biomarker selected from the second group according to one of the claims 1-3.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The kit as claimed in one of the claims 9-10, comprising a mixture of the at least one standard (1) and the at least one standard (2), in particular the composition according to claim 5.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The kit as claimed in one of the claims 9-11, further comprising a lysis buffer according to one of the claims 23-25 and/or a digesting buffer according to one of the claims 23-25.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The kit as claimed in one of the claims 9-12, further comprising at least one antibody specific for a biomarker selected from the first group according to one of the claims 1-3 and/or at least one antibody specific for a biomarker selected from the second group according to one of the claims 1-3, and reagents effective to detect said biomarker(s) in a serum sample.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The kit as claimed in claim 13, wherein the at least one antibody is polyclonal.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The kit as claimed in one of the claims 13-14 comprising at least one labelled secondary antibody specific for the at least one antibody of claim 9-10.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"A method of qualifying the EGFR kinase activity in a subject, comprising determining in a body fluid sample of a subject suffering from or being susceptible to cancer at least one biomarker selected from the first group according to one of the claims 1-3 and/or at least one biomarker selected from the second group according to one of the claims 1-3, \nwherein the body fluid level of the at least one biomarker of said first group being significantly higher and/or the body fluid level of the at least one biomarker of said second group being significantly lower than the level of said biomarker(s) in the body fluid of subjects without cancer associated with increased activity of EGFR is indicative of induced EGFR kinase activity in the subject.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"Method as claimed in claim 16 for predicting the response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator, \nwherein the body fluid level of the at least one biomarker of said first group being significantly higher and/or the body fluid level of the at least one biomarker of said second group being significantly lower than the level of said biomarker(s) in the body fluid of subjects without cancer associated with increased activity of EGFR is indicative that the subject will respond therapeutically to a method of treating cancer comprising administering an EGFR kinase modulator.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"Method as claimed in claim 16 for monitoring the therapeutically response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator, wherein the body fluid level of the at least one biomarker of said first group before and after the treatment and/or the body fluid level of the at least one biomarker of said second group before and after the treatment is determined, and a significant decrease of said body fluid level(s) of the at least one biomarker of said first group and/or a significant increase of said body fluid level(s) of the at least one biomarker of said second group after the treatment is indicative that the cancer patient therapeutically responds to the administration of the EGFR kinase modulator.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The method as claimed in one of the claims 16-18, wherein an immunoassay is performed, in particular by using the kit as claimed in one of the claims 9-15.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The method as claimed in claim 19, wherein at least one antibody specific for a biomarker selected from the first group according to claim 2 and/or at least one antibody specific for a biomarker selected from the second group according to claim 2, and reagents effective to detect said biomarker(s) in a serum sample is used for the immunoassay.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The method as claimed in one of the claims 16-18, wherein a peptide mass fingerprinting is performed, in particular by using the kit as claimed in one of the claims 9-12.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The method as claimed in claim 21, comprising the steps of\n - isolating a serum sample from a blood sample of a subject suffering from or being susceptible to cancer; \n - adding lysis buffer to the serum sample; \n - separating the proteins of the lysed serum sample by 2-DE gel electrophoresis; \n - excising from the gel at least one sample containing a protein of interest; \n - adding digesting buffer to the at least one excised sample; \n - determining the amount of the at least one protein of interest by analyzing the at least one digest mixture by mass spectrometry.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The method as claimed in claim 22, wherein\n - the subject is a human patient or non-human transgenic animal; and/or \n - the serum sample is isolated by centrifuging the blood sample; and/or \n - the 2-DE is performed by using two different pH gradients; and/or \n - the lysis buffer comprises (a) at least one buffer component, (b) at least one chaotrope, (c) at least one detergens, (d) at least one reducing agent (e) at least one carrier ampholyte, (f) at least one ribonuclease; and/or \n - the protein of interest is a biomarker selected from the first group according to one of the claims 1-3 or a biomarker selected from the second group according to one of the claims 1-3; and/or \n - the digesting buffer comprises a bicarbonate compound and a protease; and/or \n - wherein the mass spectrometry is selected from the group consisting of MALDI-TOF and ESI-TOF.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The method as claimed in one of the claims 22- 23, wherein\n - the subject is suffering from or is susceptible to cancer in particular cancer of the liver, lung, breast, colon, prostate, bladder, head and neck, ovary or brain.; and/or \n - the 2-DE is performed by using the pH gradients 3-10 and 4-7; and/or \n - the lysis buffer is an aqueous solution of (a) at least one buffer compound selected from the group consisting of Tris and HEPES, (b) at least one chaotrope selected from the group consisting of urea and thiourea, (c) at least one detergens selected from the group consisting of CHAPS and SDS, (d) at least one reducing agent selected from the group consisting of DTT and TCEP, (e) at least one carrier ampholyte selected from the group consisting of biolyte 5-7 and biolyte 3-10, (f) at least one ribonuclease selected from the group consisting of endonuclease and exonuclease; and/or \n - the protein of interest is a biomarker selected from the first group according to one of the claims 2-3 or a biomarker selected from the second group according to one of the claims 2-3; and/or \n - the digesting buffer is an aqueous solution of at least one bicarbonate compound selected from the group consisting of ammonium bicarbonate and sodium bicarbonate and of at least one serine protease, in particular selected from the group consisting of trypsin, chymotrypsin and elastase; and/or \n - the mass spectrometry is performed by MALDI-TOF; and/or \n - a tandem mass spectrometer is used; and/or \n - a matrix is used for the mass spectrometry selected from the group consisting of 3,5-dimethoxy-4-hydroxycinnamic acid, α-cyano-4-hydroxycinnamic acid and 2,5-dihydroxybenzoic acid.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The method as claimed in one of the claims 22-24, wherein\n - the subject is a transgenic mouse, in particular a mouse whose genome comprises a non natural IgEGF sequence; and/or \n - the lysis buffer is an aqueous solution of (a) Tris; (b) urea and thiourea, (c) CHAPS, (d) DTT, (e) biolyte 3-10, (f) endonuclease; and/or \n - the serum sample is calibrated or the serum samples are equilibrated to a predefined protein concentration by adding the lysis buffer; and/or \n - the protein of interest is a biomarker selected from the first group according to claim 3 or a biomarker selected from the second group according to claim 3; and/or \n - the digesting buffer is an aqueous solution of ammonium bicarbonate and trypsin; and/or \n - a MALDI-TOF/TOF spectrometry is performed; and/or \n - a matrix is used for the mass spectrometry selected from the group consisting of α-cyano-4-hydroxycinnamic acid.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The method as claimed in one of the claims 22-25, further comprising the steps of\n - determining the protein concentration of the serum sample, in particular by the Bradford method; and/or \n - freezing and thawing the serum sample before the lysis buffer is added; and/or \n - staining the gel after the 2-DE, in particular by using coomassie blue; and/or \n - destaining the exised sample; and/or \n - shrinking, in particular by adding acetonitrile, and drying of the excised sample before the digesting buffer is added; and/or \n - using a peptide calibration standard for the mass spectrometry.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"A procedure to screen for and to identify drugs against cancer associated with an increased EGFR kinase activity comprising determining in a body fluid sample of a transgenic cancer mouse being treated with a compound to be tested, in particular of a mouse whose genome comprises a non natural IgEGF sequence, at least one biomarker selected from the first group according to one of the claims 1-3 and/or at least one biomarker selected from the second group according to one of the claims 1-3, wherein the body fluid level of the at least one biomarker of said first group being significantly lower and/or the body fluid level of the at least one biomarker of said second group being significantly higher than the level of said biomarker(s) in the body fluid of an untreated transgenic cancer mouse is indicative of the therapeutic effect of said compound as a EGFR kinase modulator.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"},{"text":"The procedure as claimed in claim 27, wherein the method as claimed in claim 18, in particular according to one of the claims 19-26, is used.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"}]},"claim_lang":["en"],"has_claim":true,"description":{"en":{"text":"The invention is directed to biomarkers for determining the EGFR kinase activity in a subject, and the use thereof for predicting and monitoring therapeutic intervention in cancer patients. Areas of application are the life sciences: biology, biochemistry, biotechnology, medicine and medical technology. The epidermal growth factor receptor (EGFR) plays an important role in various tumor diseases. Its hyperactivity can cause cancer of numerous organs, e.g. epithelial tumors of the lung, colon, breast, head and neck, ovarian, and liver (HCC). The hepatocellular carcinoma (HCC), for instance, ranks fifth among the most common malignant tumors worldwide and is the third leading cause of cancer-related deaths. Thereby, the number of HCC diseases in Europe and the United States steadily increases, as exemplarily demonstrated in the north east of Germany, where the number of HCC-incidences of males arose from 3.6% in 1976 to 5.7% in 2002 . Chronic liver disease, which lead to cirrhosis and infection with hepatitis C are important risk factors for HCC. Overall, the formation of HCC is a multistage process, whereby the latest findings from cancer research evaluate the dysregulation of tumor progenitor genes as a predisposing or initial event leading to an epigenetic modification of progenitor or stem cells. Then, the risk of malignant transformation becomes dramatically increased by mutations in such tumor suppressor- and proto-oncogenes .Finally, the malignant transformation and the invasive tumor growth is massively promoted by epigenetic instability. Despite numerous findings the molecular basis of hepatocellular carcinoma remains insufficiently known. Recently, the consequences of excessive EGF-signal transmission in liver cancer has been reported. This growth factor binds to and induces EGFR activity. Activated EGFR phosphorylates many proteins which are networked by signal transduction chains and therefore favour the emergence and further development of tumor malignancies. In particular, various tyrosine residues are phosphorylated, which subsequently act as docking sites for a number of proteins. In this way, EGFR is involved in diverse signaling pathways, including the mitogen-activated protein kinases (MAPK). This in turn has implications for the fate of the cell, leading to exaggerated proliferation, the lack of differentiation and migration of transformed tumor cells. Since the EGF-receptor tyrosine kinase (RTK) plays a key role in malignant tumor diseases, therapeutic antibodies and small molecules, also termed as \"EGFR kinase modulators\", that counter an increased activity of EGFR are frequently used for the treatment of cancer. However, besides to the EGF-signalling cascade further signalling pathways are involved in the formation and growth of cancer such as, e.g., Wnt- β -Catenin, Hedgehog and other receptor tyrosine kinases. \nThus, there is a need for new prognostic and predictive biomarkers and methods for easily identifying the indication \"EGFR hyperactivity\" or \"EGFR overexpression\", repectively, in a subject suffering from or being susceptile to cancer, for accurately predicting and monitoring the response of the subject to a treatment with EGFR modulators, thereby enabeling an individualized cancer treatment of the subject for enhancing its chances of survival. The aim of the present invention is therefore to provide biomarkers, compositions and a kit, as well as a method for a fast, easy and efficient qualification or quantification of the EGFR kinase activity status of a subject suffering from or being susceptible to cancer, in particular for predicting and monitoring the response of a cancer patient to the treatment with an EGFR activity modulator. To this end, the implementation of the embodiments and actions as described in the claims provides appropriate means to fulfill these demands in a satisfying manner. The invention is based on the surprising finding that biomarkers selected from a first group consisting of Amy 1, Apo Al, Carbx, Casp, AFP, ApoM, SAP, Fib-a, Fib-b, Fib-g, ApoE, A2MG, A2MG isoform, Serpin, Clusterin, MHC-fB, SAP isoform, or from a second group consisting of Gpx3, properidin, MUP1, HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C, are regulated by EGF overexpression in subjects suffering from or being susceptilbe to cancer. The biomarkers according to the invention concern gene products of mammalia, preferably gene products of the genome of mus musculus or homo sapiens, in particular the respective gene products of homo sapiens are preferred. Within the context of the invention, the term \"subject\" is directed to a mammal, in particular to a mouse or a human being suffering from or being susceptible to cancer, more particular to a human cancer patient or a transgenic cancer mouse, such as a HCC patient or a EGF-transgenic mouse may be. The invention further concerns a composition for qualifying the EGFR kinase activity in a subject suffering from or being susceptible to cancer, in particular by an in vitro body fluid analysis, wherein the composition comprises an effective amount of at least one biomarker selected from the first group of said biomarkers or an effective amount of at least one biomarker selected from the second group of said biomarkers. In one embodiment of the invention, the biomarker is preferably selected from a first group consisting of Amy 1, Apo Al, Carbx, Casp, Fib-a, Fib-b, Fib-g, Clusterin, MHC-fB, SAP isoform or from a second group consisting of HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C. In another preferred embodiment, the biomarker is selected from a first group consisting of AFP, ApoE, ApoM, or from a second group consisting of Gpx3, A2MG, A2MG isoform, SAP. In particular, it is preferred, if the composition according to the invention comprises an effective amount of at least one biomarker selected from the first group of said biomarkers and an effective amount of at least one biomarker selected from the second group of said biomarkers, wherein the combination\n (a) biomarker selected from the group consisting of Amy 1, Apo Al, Carbx, Casp, Fib-a, Fib-b, Fib-g, Clusterin, MHC-fB, SAP isoform and biomarker selected from the group consisting of HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C or the combination (b) biomarker selected from the group consisting of AFP, ApoE, ApoM and biomarker selected from the group consisting of Gpx3, A2MG, A2MG isoform, SAP is particularly preferred. \nIn another preferred embodiment the composition further comprises an effective amount of a biomarker selected from the group of EGF, thus allowing an easy calibration of the system. \nIn yet another preferred embodiment, the composition according to the invention further comprises an effective amount of a protease, in particular of trypsin, thus enabling a further enhancement of the system sensitivity. \nThe composition according to the invention, in particular the protease digest thereof, may be preferably used for producing a vaccine for the immunization of an animal in order to produce polyclonal antibodies specific for the at least one biomarker. \nAnother aspect of the invention concerns the use of the composition according to the invention for the production of a diagnostic agent, in particular of a diagnostic standard for in vitro body fluid analyses. \nThe term \"body fluid\" according to the invention is directed to any body fluid of a subject, in particular to blood, plasma, serum or urine, whereas serum is the preferred body fluid within the context of the invention. The term \"diagnostic agent\" as used herein relates to any solution, suspension or solid formulation, containing said composition in an acceptable amount for diagnostic purposes. \nIn particular, the composition is used for the production of a diagnostic agent for qualifying the EGFR kinase activity in a subject suffering from or being susceptible to cancer, preferably cancer of the liver, lung, breast, colon, prostate, bladder, head and neck, ovary or brain, in particular in a subject suffering from or being susceptible to HCC. \nIn a further preferred embodiment, the composition according to the invention is used for the production of a diagnostic agent for predicting or monitoring the response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator to the patient. \nIn yet another aspect, the invention provides a kit for qualifying the EGFR kinase activity in a subject suffering from or being susceptible to cancer, in particular for predicting or monitoring the response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator, wherein the kit comprises at least one standard (1) indicative of the body fluid level of a biomarker selected from the first group of said biomarkers in normal individuals or individuals having cancer associated with increased EGFR kinase activity and/or at least one standard (2) indicative of the body fluid level of a biomarker selected from the second group of said biomarkers in normal individuals or individuals having cancer associated with increased EGFR kinase activity, and instructions for the use of the kit. \nIn a preferred embodiment of the kit, the standard (1) comprises an indicative amount of at least one biomarker selected from the first group of said biomarkers and/or the at least one standard (2) comprises an indicative amount of at least one biomarker selected from the second group of said biomarkers. \nIn another preferred embodiment, the kit comprises a mixture of the at least one standard (1) and the at least one standard (2), in particular a composition according to the invention comprising an effective amount of at least one Figure 3 from the first group of said biomarkers and an effective amount of at least one biomarker selected from the second group of said biomarkers, wherein the set of biomarkers according to combination (a) or combination (b), as described herein, is particularly preferred. \nIn yet another preferred embodiment, the kit according to the invention further comprises a lysis buffer, wherein the lysis buffer comprises (a) at least one buffer component, (b) at least one chaotrope, (c) at least one detergens, (d) at least one reducing agent (e) at least one carrier ampholyte, and (f) at least one ribonuclease, Preferably, the lysis buffer is an aqueous solution of (a) at least one buffer compound selected from the group consisting of Tris and HEPES, (b) at least one chaotrope selected from the group consisting of urea and thiourea, (c) at least one detergens selected from the group consisting of CHAPS and SDS, (d) at least one reducing agent selected from the group consisting of DTT and TCEP, (e) at least one carrier ampholyte selected from the group consisting of biolyte 5-7 and biolyte 3-10, and (f) at least one ribonuclease selected from the group consisting of endonuclease and exonuclease, wherein an aqueous solution of (a) Tris; (b) urea and thiourea, (c) CHAPS, (d) DTT, (e) biolyte 3-10, and (f) endonuclease, is particularly preferred. In one preferred embodiment, the kit according to the invention further comprises at least one antibody specific for a biomarker selected from the first group of said biomarkers and/or at least one antibody specific for a biomarker selected from the second group of said biomarkers, and reagents effective to detect said biomarker(s) in a serum sample, such as buffers for dissolving or equilibrating the standard (1) and/or the standard (2), or an enzyme substrate for imaging enzyme labels may be. In particular, a kit is preferred, comprising at least one antibody specific for a biomarker selected from the group consisting of Amy 1, Apo Al, Carbx, Casp, Fib-a, Fib-b, Fib-g, Clusterin, MHC-fB, SAP isoform and/or at least one antibody specific for a biomarker selected from the group consisting of HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C. \nMore particular, it is preferred, if the at least one antibody is polyclonal, thus allowing a further enhancement of the system sensitivity. \nAdvantageously, the kit further comprises at least one labelled secondary antibody specific for the at least one antibody, thus allowing a fast screening of the binding of the at least one antibody to the at least one biomarker, in particular if the at least one biomarker or the digest thereof is immobilized to a solid phase support, such as nitrocellulose may be. In a further aspect, the invention provides a method of qualifying the EGFR kinase activity in a subject, comprising determining in a body fluid sample of a subject suffering from or being susceptible to cancer at least one biomarker selected from the first group of said biomarkers and/or at least one biomarker selected from the second group of said biomarkers, wherein the body fluid level of the at least one biomarker of said first group being significantly higher and/or the body fluid level of the at least one biomarker of said second group being significantly lower than the level of said biomarker(s) in the body fluid of subjects without cancer, in particular without cancer associated with increased activity of EGFR, is indicative of induced EGFR kinase activity in the subject. In particular, it is preferred, if the method comprises determining at least one biomarker selected from the first group of said biomarkers and at least one biomarker selected from the second group of said biomarkers, wherein the body fluid level of the at least one biomarker of said first group being significantly higher and the body fluid level of the at least one biomarker of said second group being significantly lower than the level of said biomarkers in the body fluid of subjects without cancer, in particular without cancer associated with increased activity of EGFR, is indicative of induced EGFR kinase activity in the subject, preferably if a combination of a biomarker selected from the group consisting of Amy 1, Apo Al, Carbx, Casp, Fib-a, Fib-b, Fib-g, Clusterin, MHC-fB, SAP isoform and a biomarker selected from the group consisting of HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C or a combination of a biomarker selected from the group consisting of AFP, ApoE, ApoM and a biomarker selected from the group consisting of Gpx3, A2MG, A2MG isoform, SAP is determined. Preferably, the method according to the invention is carried out for predicting the response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator, wherein the body fluid level of the at least one biomarker of said first group being significantly higher and/or the body fluid level of the at least one biomarker of said second group being significantly lower than the level of said biomarker(s) in the body fluid of subjects without cancer, in particular without cancer associated with increased activity of EGFR, is indicative that the subject will respond therapeutically to a method of treating cancer comprising administering an EGFR kinase modulator. In one embodiment, the method is implemented for monitoring the therapeutically response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator, wherein the body fluid level of the at least one biomarker of said first group before and after the treatment and/or the body fluid level of the at least one biomarker of said second group before and after the treatment is determined, and a significant decrease of said body fluid level(s) of the at least one biomarker of said first group and/or a significant increase of said body fluid level(s) of the at least one biomarker of said second group after the treatment is indicative that the cancer patient therapeutically responds to the administration of the EGFR kinase modulator. In a preferred embodiment, the method is implemented by performing an immunoassay, such as an enzyme immunoassay (EIA), a radio immunoassay (RIA) or a fluorescence immunoassay (FIA) may be, in particular by using the kit according to the invention and/or by performing a western blot. Preferably, at least one antibody specific for a biomarker selected from the group consisting of Amy 1, Apo Al, Carbx, Casp, Fib-a, Fib-b, Fib-g, Clusterin, MHC-fB, SAP isoform and/or at least one antibody specific for a biomarker selected from the group consisting of HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C is used for the immunoassay and/or reagents effective to detect said biomarker(s) in a serum sample, such as a blocking buffer for reducing unspecific antibody binding or an enzyme substrate for imaging enzyme labelled antibodies may be, is used for the immunoassay. In another preferred embodiment, the method is implemented by performing a peptide mass fingerprinting, in particular by using the kit described herein. Within the context of peptide mass fingerprinting, the method preferably comprises the steps of\n isolating a serum sample from a blood sample of a subject suffering from or being susceptible to cancer, adding lysis buffer to the serum sample; separating the proteins of the lysed serum sample by 2-DE gel electrophoresis; excising from the gel at least one sample containing a protein of interest; adding digesting buffer to the at least one excised sample, and determining the amount of the at least one protein of interest by analyzing the at least one digest mixture by mass spectrometry. In one embodiment of the method, the subject is a human patient or a non-human transgenic animal, in particular suffering from or being susceptible to cancer, more particular suffering from or being susceptible to cancer of the liver, lung, breast, colon, prostate, bladder, head and neck, ovary or brain, such as a transgenic mouse, in particular a mouse whose genome comprises a non natural IgEGF sequence, may be. In another embodiment of the method, the serum sample is isolated by centrifuging the blood sample; In yet another embodiment of the method, the 2-DE is performed by using two different pH gradients, preferably by using the pH gradients 3-10 and 4-7. In a further embodiment of the method, the lysis buffer comprises (a) at least one buffer component, (b) at least one chaotrope, (c) at least one detergens, (d) at least one reducing agent (e) at least one carrier ampholyte, and (f) at least one ribonuclease. Preferably, the lysis buffer used is an aqueous solution of (a) at least one buffer compound selected from the group consisting of Tris and HEPES, (b) at least one chaotrope selected from the group consisting of urea and thiourea, (c) at least one detergens selected from the group consisting of CHAPS and SDS, (d) at least one reducing agent selected from the group consisting of DTT and TCEP, (e) at least one carrier ampholyte selected from the group consisting of biolyte 5-7 and biolyte 3-10, and (f) at least one ribonuclease selected from the group consisting of endonuclease and exonuclease, wherein an aqueous solution of (a) Tris; (b) urea and thiourea, (c) CHAPS, (d) DTT, (e) biolyte 3-10, and (f) endonuclease, is particularly preferred.the lysis buffer comprises (a) at least one buffer component, (b) at least one chaotrope, (c) at least one detergens, (d) at least one reducing agent (e) at least one carrier ampholyte, (f) at least one ribonuclease is particularly preferred. In yet a further embodiment of the method, the protein of interest is a biomarker selected from the first group of said biomarkers or is a biomarker selected from the second group of said biomarkers, in particular is selected from the first group consisting of Amy 1, Apo Al, Carbx, Casp, Fib-a, Fib-b, Fib-g, Clusterin, MHC-fB, SAP isoform or from the second group consisting of HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C, or more preferably is selected from the first group consisting of AFP, ApoE, ApoM or from the second group consisting of Gpx3, A2MG, A2MG isoform, SAP. In another embodiment of the method the digesting buffer comprises a bicarbonate compound and a protease, wherein the digesting buffer preferably is an aqueous solution of at least one bicarbonate compound selected from the group consisting of ammonium bicarbonate and sodium bicarbonate and of at least one serine protease, in particular selected from the group consisting of trypsin, chymotrypsin and elastase, or, in particular preferred, the digesting buffer is an aqueous solution of ammonium bicarbonate and trypsin. In yet another embodiment of the method, the mass spectrometry is selected from the group consisting of MALDI-TOF and ESI-TOF, preferably the mass spectrometry is performed by MALDI-TOF. In a further embodiment of the method, a tandem mass spectrometer is used for the peptide mass fingerprinting, wherein a MALDI-TOF/TOF spectrometry is particularly preferred for putting the method into practice. In yet a further embodiment of the method, a matrix is used for the mass spectrometry selected from the group consisting of 3,5-dimethoxy-4-hydroxycinnamic acid, α-cyano-4-hydroxycinnamic acid and 2,5-dihydroxybenzoic acid, wherein α-cyano-4-hydroxycinnamic acid is particularly preferred as the matrix. In another preferred embodiment of the method, the serum sample is calibrated or the serum samples are equilibrated to a predefined protein concentration by adding the lysis buffer, thus allowing an easy adaption of the system to different purposes. In particular, it is preferred, if the method further comprises the steps of \n- determining the protein concentration of the serum sample, in particular by the Bradford method; or \n- freezing and thawing the serum sample before the lysis buffer is added; and/or \n- staining the gel after the 2-DE, in particular by using coomassie blue; and/or \n- destaining the exised sample; or \n- shrinking, in particular by adding acetonitrile, and drying of the excised sample before the digesting buffer is added; or \n- using a peptide calibration standard for the mass spectrometry, \nwherein preferably a combination of said steps, in particular two of said steps, more preferably three of said steps, in particular four or five of said steps, most preferably all of said steps are implemented. Yet another aspect of the invention concerns a procedure to screen for and to identify drugs against cancer associated with an increased EGFR kinase activity, wherein the procedure comprises determining in a body fluid sample of a transgenic cancer mouse being treated with a compound to be tested, in particular of a mouse whose genome comprises a non natural IgEGF sequence, at least one biomarker selected from the first group of said biomarkers and/or at least one biomarker selected from the second group of said biomarkers, and wherein the body fluid level of the at least one biomarker of said first group being significantly lower and/or the body fluid level of the at least one biomarker of said second group being significantly higher than the level of said biomarker(s) in the body fluid of an untreated transgenic cancer mouse is indicative of the therapeutic effect of said compound as an EGFR kinase modulator. In a preferred embodiment, the procedure is implemented by using the method according the invention, in particular by using the method comprising an immunoassay or a peptide mass fingerprinting as described herein. Further scope of applicability of the present invention will become apparent from the detailed description given hereinafter. However, it should be understood that the detailed description and specific examples, while indicating preferred embodiments of the invention, are given by way of illustration only, since various changes and modifications within the spirit and scope of the invention will become apparent to those skilled in the art from this detailed description. Epidermal growth factor (EGF) is an important mitogen for hepatocytes. It's targeted overexpression induced hepatocellular carcinomas (HCC), as recently reported by us (Borlak et al. 2005). Early detection of disease is essential for successful therapy and overall survival. In particular, the efforts in identifying serum biomarkers of liver cancer in a transgenic disease model that mimics effectively the consequence of exaggerated EGF signalling are described. A reference 2-DE map of mouse serum proteins is reported. About 180 proteins were detected per gel and 130 proteins were identified by 2-DE-MALDI-MS analysis. Serum proteins of healthy non-transgenic and HCC tumor bearing mice were compared and 25 regulated proteins were identified, of which n= 7 reached statistical significance (p<0.05). Furthermore, several fragments of fibrinogens and of the alpha-2-macroglobulin were identified to be disease associated. Also immunoglobulins were found to be repressed or absent in serum samples of tumor bearing mice, and this included, amongst others, the Ig K and L class. In contrast, amyloid component P and apolipoprotein M were highly significantly increased by 10- and 8- fold, respectively in serum samples of HCC-mice. Overall, the findings provide a rationale for further clinical evaluation of the herein identified biomarker candidates. In the following, the findings with an EGF transgenic disease model of liver cancer are reported. This is an important growth factor mitogen for hepatocytes. Its targeted overexpression promoted hepatocellular carcinogenesis as recently reported by us. 8 In general, the EGF gene codes for a 53 amino acid protein to stimulate proliferation of epidermal cells and a variety of other cell types through binding to the EGF receptor. This single-pass transmembrane receptor functions as a tyrosine kinase. Once activated, the EGFR becomes autophosphorylated to initiate signalling through tyrosine phosphorylation of other proteins. 9 A total of four different EGF receptors (Her1, Her2, Her3, Her4) have been identified so far. Specifically, ligand binding induces either homo- and/or heterodimerisation. It is of considerable importance that EGFR connects to other signalling cascades as well, notably the MAP kinase pathway, to ultimately cause phosphorylation of transcription factors such as c-Fos, c-Jun and ELK-1, thereby fostering cell proliferation. 9 EGFR is over expressed in a number of solid tumours and the expression level correlates well with tumour progression, resistance to chemotherapy and survival. Consequently, EGFR is an obvious target for the rational design of novel anticancer agents, i.e. inhibitors of the receptor kinase activity and/or antagonistic antibodies. 10 Previously, targeted overexpression of a secretable form of EGF (IgEGF) has been reported to result in multiple highly malignant HCCs, with 100% fatalities around 7-8 months after birth . 11 This transgenic mouse line mimics effectively the consequence of an altered EGF and/or TNFα signalling. Recently, other mice models were successfully established to study the tumor biology of HCC in non-viral- and viral disease 12-13 . Through application of gene chip analysis it was possible to identify networks of EGF-regualted genes at various stages of tumour development. 8 Here, the efforts to examine serum proteins of non-transgenic healthy and EGF overexpressing transgenic mice are reported. A reference 2-DE map of mouse serum proteins, consisting of more than 130 proteins, was created . After 2-DE analysis and gel image matching, 25 serum proteins were identified by peptide mass fingerprinting as being disease associated. These proteins are involved in a variety of cellular and metabolic pathways, amongst them: the glutathione peroxidase 3 (Gpx3) and the serum amyloid component P (SAP), their expression being up-regulated by up to 10-fold in tumour bearing mice. \nOverall, this study aimed at identifying disease associated serum proteins in an EGF liver cancer disease model. The serum proteome of healthy and HCC tumor bearing mice was investigated . As depicted in Figure 1A , transgenic mice overexpressed EGF by approximately 26-fold. Furthermore, tumors were confirmed by histopathology, of which an example is given in Fig. 1B . Essentially, highly differentiated tumors were observed which were less differentiated at advanced stages of disease (see also Borlak et al., 2005 for further details). 8 A total of 14 2-DE gels (n = 5 independent serum control and n = 9 independent serum of HCC mice) were processed for MALDI-TOF-MS analysis (see supplementary material 1, Fig. 5 ). This enabled the built up of a reference 2-D map of mouse serum proteins consisting of 130 proteins ( Fig. 2A ). 25 proteins were found to be differentially regulated of which n= 7 were statistically significant (Table 1, Fig. 2B , C ). Albumin is the most abundant serum protein ; its quantification of the 2-DE gels gave a relative volume of approximately 34 % (see supplementary material 2, Fig. 6 ). Other high abundance proteins include alpha-2-macroglobulin with a relative volume of 10 %, transferrin (7 %), apolipoprotein A1 (4 %), plasminogen (4 %) and several immunoglobulins (Igs) such as H-C, K and L (4 %). Less abundant proteins were apolipoprotein E, apolipoprotein H, fibronectin, gelsolin, kininogen and ceruloplasmin. Several spots were identified at low molecular weights as albumin or fragments of it ( Figure 2 A) and more than 8 spots as alpha-2-macroglobulin (A2MG) (fragments) with mass ranges of 37-40 kDa (A2mG has a Mr of ∼ 165 kDa). At least 2 of these fragments were up-regulated in serum of tumour bearing mice and were increased by 3-fold (see table 1, Fog. 3E, supplementary material 8, Fig. 12 ). Furthermore, two isoforms were identified with identical pl but different Mr as well. \nAdditionally, the apolipoproteins Apo A-I, Apo E, Apo H, ApoM and ApoJ were identified. 6 different spots in the serum proteome maps were observed, which were identified by MALDI-TOF as Apo A-I (see supplementary material 3, Fig. 7 ) and at least 5 spots of apo H, also known as beta-2-glycoprotein I (see supplementary material 4, Fig. 8 ). After in gel digestion, approximately 2500 spots were selected for MALDI-TOF-PMF analysis. In the supplementary table 1 accession number, protein name, theoretical pl and Mr together with Mascot score, identified peptides and sequence coverage are given. Furthermore, biological function, frequency of identification and protein expression in serum of tumor and / or healthy mice are summarized as well (see supplementary table 1). Among the 130 annotated proteins, 25 were differentially expressed (Table 1), of which 7 were up-regulated (apolipoprotein E, alpha-2-macroglobulin, alpha-2-macroglobulin *, alfafetoprotein, apolipoprotein M, serum amyloid component P, serine proteinase inhibitor) ( Fig. 3C, 3E ), where as 3 proteins were down-regulated (glutathione peroxidase 3, properdin, major urinary protein 1) ( Fig. 3A ). Moreover, 10 proteins were found in serum of tumor bearing mice only (amylase 1, apo A-I, carboxylesterase, caspase, clusterin, fibrinogen-α, fibrinogen-β, fibrinogen-γ, major histocompatibility complex factor B, serum amyloid component P*), but 5 proteins were exclusively identified in serum sample of healthy control animals (mannose binding lectin A, orosomucoid 1, HMW-kininogen II, leukemia inhibitory factor receptor, mannose binding protein-C) ( Fig. 3G ). \nIn tumor bearing mice, most of the up-regulated serum proteins are apolipoproteins. Among them, apoM was up-regulated by 8-fold ( Fig. 3C , 4B , supplementary material 6, Fig. 10 ). ApoM is seen as an important biomarker candidate and its significance is discussed later on. Furthermore, apolipoproteins are closely associated with amyloid fibrillogenesis. Indeed, serum amyloid A, apolipoprotein (apo) All and apo A1 are deposited as biochemically distinct forms of amyloid. 14 In serum samples of HCC bearing mice, the serum amyloid component P (SAP) was strongly increased. This protein belongs to the group of acute-phase reactants (APRs) ( Fig. 3C , 4D ). Here SAP is evidenced to be highly disease associated in HCC and a putative isoform (SAP*) in sera of tumour bearing mice is identified (see table 1, supllemantary material 7) with a lower theoretical pl value. \nIn addition, several isoforms of alpha-2-macroglobulin were found (see Fig. 2A , supplementary material 8, Fig. 12 ) to be induced in HCC. To the best of our knowledge, the overexpression of the newly identified fragments have not been reported for HCC so far. In general, the serum concentration of A2MG is about 2 g/l in adults but displays little variation with age or in acute and chronic disease. It therefore may qualify as a bonafide candidate serum biomarker for HCC. \nFurther, decreased concentration of proteins of the acute phase response in serum of HCC mice were observed . This group of proteins, designated as negative acute phase proteins, included major urinary protein 1 (MUP1), glutathione peroxidase 3 (Gpx3), properdin, and several immunoglobulins (Igs). (see table 1 , Fig. 3A ). Specifically, plasma glutathione peroxidase 3 (Gpx3), a glycosylated protein, was repressed when serum samples from healthy non-transgenic and tumor bearing mice were compared. In 2D gels two different spots are visible e.g. Gpx3* and Gpx3 while only one isoform was repressed in serum samples of tumour bearing mice (Gpx3) (see Fig. 3A , supplementary material 9, Fig. 13 ). \nIn the present study, also cancer-related fibrinogen deposition in serum of HCC bearing mice is identified (see table 1, Fig. 3D , supplementary material 10, Fig. 14 ). Plasmin-generated fragments of fibrinogen alpha, beta and gamma (Fga, Fgb, Fgg) were already observed in various types of solid tumor types. In fact, elevated levels of Fgg and acute phase proteins were reported for plasma proteins of prostate-, lung-, and breast-cancer patients. 15-16 As of today overexpression of FGG was reported for two hepatoma cell lines, e.g. SMMC-7721 and HepG2. 17 Up-regulation of Fgg in EGF induced HCC is now evidenced, as well. Specifically, not all tumor samples expressed the three fibrinogens (see Figure 4A , supplementary material 10, Fig. 14 ), but this agrees well with the findings of Gerner et al., who reported Fgg to be present in 58 % of the cases (14 / 24 analyzed plasma cancer samples. 15-16 Elevated plasma levels of Fgg, as observed in serum of EGF transgenic mice may be viewed as indicators for tumor-associated fibrin deposition and fibrinolysis. Fibrinolysis is mediated mainly via the plasma protease plasmin, which exerts pleiotropic effects. 18-20 Furthermore, the complement system is known to contain at least 30 different proteins, which are primarily formed in the liver and circulate in their inactive form. These proteins, when activated, produce various complexes that play a major role in the natural defense mechanisms of the human body. Several proteins of the complement system were identified to be regulated. This included the mannose binding lectine A and the mannose binding protein C (present in serum of healthy non-transgenic mice only), and the major histocompatibility complex factor B (MHC-fB) which was found to be up regulated. MHC-fB was identified in healthy and HCC serum samples, but an activated form/fragment of this protein was found in serum of HCC mice only in the range of Mw 65-68 kDa (see table 1, Fig. 3F ). These fragments could be the result of proteolitic processes in tumours. \nAlso, orosomucoid 1, also known as alpha 1-acid glycoprotein, was identified in sera of health non tumor bearing animals (see table 1, Fig. 3G ). This protein is synthesised by the liver, and functions in modulating the activity of the immune system during the acute-phase reaction. Several studies report an up regulation of this protein in patients with HCC and suggest orosomucoid as a useful marker for discriminating the stage of inflammatory reactions. 21-23 Finally, an up regulation of the oncofetal protein Afp was observed in sera of HCC-mice ( Fig. 3C , 4C ). Indeed, Afp is routinely assayed for liver damage and its malignancies. To confirm results by different means, 4 proteins regulated in all gels were selected for Western Blot analysis. A total of n = 5 serum samples of tumor bearing mice were probed for Fib-γ, ApoM, Afp ( Fig. 4 A,B,C ), where as n= 4 serum samples was used for SAP ( Fig. 4 D) . Fib-γ was expressed only in 3 out of the 5 serum samples analyzed. Serum biomarkers of HCC were searched for and a serum proteome map of EGF induced HCC is reported. Comparison between sera of healthy and tumour animals revealed significant differences in expression of several proteins. A total of 25 proteins was identified as differentially expressed. Specifically, proteins of the acute phase response were found to be down regulated. This group of proteins included mannose binding lectin a (MBL-A), major urinary protein 1 (MUP 1), orosomucoid 1 (Orm1), glutathione peroxidase 3 (Gpx3) and several immunoglobulins (Igs) (see table 1, supplememntary material 11). In contrast, Apo E was up regulated in serum of HCC mice.Notably, Yokoyama and coworkers observed increased expression of apo E in 88 % of HCC tumor tissue without an increase of apo E gene expression and / or elevated serum level. 19 These results do not agree with the findings as serum levels of apo E were increased by 2-fold ( Fig. 3E and supplementary material 5, Fig. 9 ). An overexpression of ApoE has already been observed in brain 24 , breast 25 , ovarian 26 , prostate 27 and HCC tumor tissues. 28 Another up-regulated apolipoprotein was apoM. This protein is mainly associated with high-density lipoprotein (HDL) in human plasma, and a small proportion in triglyceride-rich (TGRLP) and low-density lipoproteins (LDL). During embryogenesis, apo M is over expressed in livers of 3-5 month-old human embryos and continues to be strongly expressed throughout embryogenesis, but thereafter returns to much lower levels. Apo M is found as an important biomarker candidate. Furthermore, there is evidence for platelet-activating factor (PAF) to be involved in the up-regulation of apo M in HepG2 cells, but Luo and coworkers reported decreased apo M mRNA transcript levels in HepG2 cells in response to epidermal growth factor (EGF) treatment. 29-30 It is of considerable importance that apo M gene expression may also be regulated by hepatocyte nuclear factor-1α (HNF-1α), which was found to be repressed in tumor tissue of EGF transgenic mice (results of Western Blot not shown). 31 Furthermore, the apo M gene is located within the histocompatibility complex III (HMC-III) region of chromosome 6 and many genes in this region code for immune response. 30 Whether apo M is co-regulated by the host defense system requires additional research. \nIn general, apolipoproteins are important in maintaining the structural integrity of lipoprotein particles thereby facilitating the solubilisation of lipids. Additionally, they play a crucialrole in lipoprotein receptor recognition and regulation of lipoprotein metabolism. In humans, about 60 % of the protein content in high-density lipoprotein (HDL) is represented by apo A-I and about 20 % by apo A-II. Other apolipoproteins include apo A-IV, apo C, apo D and apo E. Most of these proteins are expressed as different isoforms. Recently, it was suggested that apo A-I exists in six isoforms, 4 of them displaying differences in glycosylation pattern. 32 Likewise, apo-H displays genetic polymorphism, with three alleles, namely APOH*1, APOH*2, APOH*3, at a single locus on chromosome 17. 33 This protein has been identified as a structural component of chylomicrons, very low-density lipoproteins (VLDL), low-density lipoproteins (LDL) and HDL. In human plasma, 35 % of apo-H is associated with chylomicrons. 34 Various properties have been ascribed to this protein, e.g. function as an antigen of antiphospholipid antibodies, or acute-phase reactant and may have some involvement in the HBV infection of hepatocytes as well . 35-36 Our study identified A2MG to be strongly upregulated in HCC. This protein is an abundant plasma protein produced predominantly by the mammalian liver. A2MG is a member of the protease inhibitor 139 (A2M) family and is able to inhibit all four classes of proteinases by a unique 'trapping' mechanism located in a 'bait region', which contains specific cleavage sites for different proteinases. When a proteinase cleaves the bait region, a conformational change of the protein is induced, which then traps the proteinase. The entrapped enzyme remains still active against low molecular weight substrates, but is poorly accessible for reaction with high molecular weight substrates. Mouse A2MG has a M r of ∼165 kDa; notably, more than 8 spots as A2MG fragments with mass ranges of 37-40 kDa were identified . At least 2 of these fragments were up regulated in serum of tumor bearing mice and were increased by 3-fold (see table 1, Fig. 3E , supplementary material 8, Fig. 5 ). Furthermore, two isoforms with identical pl but different Mw were identified as well. In breast and trophoblastic cancers, A2MG may be less useful as a tumor marker. 37 In contrast, serum A2MG levels in patients with ovarian carcinomas are significantly elevated. 38-39 Likewise, the study also evidenced repression of glutathione peroxidase 3 (Gpx3) in HCC bearing mice. Gpx3 is one of at least 25 selenocysteine-containing protein with antioxidant properties in mammals. It is one of the five known glutathione peroxidases and is unique among members of the Gpx family as this protein is the only extracellular isoform. Gpx3 is secreted from renal proximal tubular cells and epithelial cells of the Bowman's capsule. While Gpx3 deficiency has been associated with cardiovascular disease and with renal dysfunction or infertility of males, little is known about its association with HCC. 40-41 Strikingly, plasma selenium concentration is decreased in patients with cirrhosis, as reported by Burk and coworkers, who investigated glutathione peroxidase (GSHPx-3) and selenoprotein P expression, in patients with cirrhosis and in healthy control subjects. 42 Equally, studies on selenium availability and expression of selenoproteins (Gpx1, Gpx3, thioredoxin reductase and selenoprotein P mRNA) in mouse fibrosarcoma cells evidenced selenium to exert a statistically significant effect on Gpx3 transcript expression. 43 Whether selenium availability is reduced in HCC requires further studies. \nAlso, high proteolytic activity in sera of HCC bearing mice was observed. Recently, Chignard et al. detected protein fragments in HCC patient sera as well, identified as calreticulin and protein disulfide isomerase A3. 44 Generally, plasma proteases are capable of activating growth factors by cleavage of their inert proforms. 45 High proteolytic activity of proteases in plasma of cancer patients has been reported. 16 This may also be linked to an overexpresion of SAP, apo M and other serum proteins in HCC bearing mice as reported in the study. An acute phase response is observed in the majority of cancer patients 46 and could represent an adaptive response to an exaggerated proteolytic activity. In fact, during tumor growth these proteins accumulate in peripheral blood and may interfere by a direct anti-apoptotic mode on tumor necrosis factor-induced apoptosis of hepatocytes as suggested by Van Molle et al, 1997. 47-48 Finally, disease associated regulation of a fragment of Factor B in serum of HCC mice was found. Factor B is a serine proteinase of the antibody-independent, alternative pathway of complement activation, an important humoral response of the host defense system against invading pathogens. In addition, fragments of the factor B exert cytokine-like activities to cause B lymphocyte proliferation and differentiation, macrophage spreading and monocyte mediated cytotoxicity. The major site of MHC-fB expression is the liver, as evidenced by allotyp changes of serum MHC-fB following liver transplantion. MHC-fB is a positive acute phase reactant. It's hepatic synthesis and serum level are increased during the acute phase of the inflammatory response. 49 Overall, serum amyloid component P (SAP), apolipoprotein M (apo M), alpha-2-macroglobulin (A2MG) and fibrinogens (Fga, Fgb, Fgg) are found as beneficial candidates for HCC-diagnostics, since their serum levels were increased by 10- , 8-and 3- fold, respectively. Furthermore, fibrinogens were identified in serum samples of HCC mice only, but their expression was variable. The current available screening tests to detect early liver malignancies combine α-fetoprotein analysis and ultrasound. Even though screening for early detection of HCC has become more common, its effectiveness in disease diagnostics remains controversial. 50 There is a need to search for new, robust and specific markers for the detection of HCC at early stages of disease to allow for curative rather than palliative interventions. Since blood serum contains high concentrations of abundant proteins such as albumin, transferrin, haptoglobin and immunoglobulins, their removal may be advantageous to enable detection and identification of less abundant proteins. Unfortunately, many of the target proteins are bound to abundant proteins; thus, depletion of serum of major proteins using affinity chromatography, specific antibodies or size-exclusion filtration may also lead to removal of less abundant proteins and therefore loss of biomarkers. In conclusion, the use of 2-DE combined with MALDI-TOF-MS, analysis provided evidence for 25 differentially expressed proteins in serum of HCC bearing mice, of which n=7 reached statistical significance. Several proteins, so far unknown to be regulated in HCC, have been identified and represent beneficial biomarkers useful for implementing the invention. Materials A UP 200S sonicator (Dr. Hielscher GmbH, Germany) was used to homogenize the samples. For the first dimension, immobilized pH-gradient (IPG) strips (17cm, pH 3-10 non linear) were purchased from Bio-Rad (Hercules, CA USA). The focusing chamber was Protean IEF Cell (Bio-Rad). For the second dimension a Protean plus Dodeca Cell (Bio-Rad) was used. Reagents: tris, urea, thiourea, CHAPS, dithiothreitol, bromophenol blue, glycerin, sodium dodecyl sulphate, glycin, temed, ammoniumperoxodisulphate, ammonium sulphate, ammonium bicarbonate, colloidal coomassie blue and acrylamide were purchased from Roth (Karlsruhe, Germany). lodacetamide was from SERVA (Heidelberg, Germany). Benzonase was purchased from Novagen (Darmstadt, Germany). Ampholytes (Biolyte 3-10) were purchased from Bio-Rad (Hercules, CA USA). Animal care The creation of the EGF2B transgenic line was described earlier by Tönjes et al. (1995). Transgenic mice were maintained as hemizygotes in the CD2F1-(DBA/2xBalb/c) background. PCR was carried out with Platinum PCRSuperMix (InVitrogen). Annealing temperature and the number of cycles are indicated in brackets after each primer pair. The transgene was verified by PCR of DNA extracted from tail biopsies (Hogan et al., 1994) and the following forward primer (fp) and reverse primer (rp) pair was used for a transgene specific amplification: forward primer: 5'-CTAGGCCAAGGGCCTTGGGGGCTCTTGCAG\n 3'; reverse primer: 5'- CATGCGTATTTGTCCAGAGCTTCGATGTA-3' (61 °C, 32 cycles, 317 bp). \nAnimals, aged 6-8 months and of the weight of 25 -33 g, were housed in Makrolon ® Type III cages. Drinking water and food (V1124-000, SSNIFF, Holand) was given ad libitum. Temperature and relative humidity were 22 ± 2 °C and 40-70 % respectively. Furthermore, a 12 h day and night cycle was used. For serum protein identification, mice were sacrificed with CO 2 and blood was taken from the Vena cava. Then, blood was centrifuged (20 min., 6000 rpm, at room temperature) and serum was immediately frozen at -80 °C. None of the serum samples were hemolytic. Sample preparation Five micro liters of sera from n=4/group non-transgenic control and from n=6/group tumor bearing animals were used for further 2-DE analysis. The protein concentration of serum was determined by the Bradford method. For each animal 0.5 mg of protein sample, approximately 3 µL of serum, were diluted to a final volume of 350 µL with a lysis buffer containing 40 mM tris base, 5 M urea, 2 M thiourea, 4 % CHAPS, 100 mM DTT, 0.5 % (v/v) biolyte 3-10 and endonuclease (6 µL / mL). Two-dimensional gel electrophoresis - 2-DE A total of n=8 2-DE gels for control serum samples and n=12 2-DE gels for serum of tumor bearing mice were prepared as follow: IEF was performed using precast 17 cm IPG strips 3-10 NL. 0.5 mg of protein was loaded by active rehydration (12 h, 50 V). Focusing started at 250 V for 20 min. in rapid mode, 10000 V for 5 h in linear mode and 10000 V for 50000 Vh in rapid mode. Each sample was analyzed in duplicate. \nAfter IEF, the IPG strips were either stored at - 80°C or transferred to 10 mL equilibration buffer (6 M urea, 30 % w/v glycerin, 2% w/v SDS, 50 mM Tris-HCl pH 8.8) with 2 % w/v DTT and 0.5 % v/v bromophenol blue solution (0.25 % w/v bromophenol blue, 1.5 M Tris-HCl pH 8.8, 0.4 % w/v SDS) and incubated for 20 min. at room temperature. Strips were removed and incubate in equilibration buffer with 4 % w/v iodoacetamide and 0.5 % v/v bromophenol blue solution for further 20 min. at room temperature. Finally, strips and 10 µL SDS-PAGE molecular weight standard on filter paper were placed on top of the 20 cm x 20.5 cm 12 % second-dimension gel (12 % v/v acrylamide/bis solution, 375 mM Tris, pH 8.8, 0.1 % v/v SDS, 1/2000 TEMED, 0.05 % v/v APS). Both were fixed in place with a 0.5 % w/v agarose overlay. Gels were run in PROTEAN Plus Dodeca cell from Bio-Rad at 70 V for approximately 14 h, followed by 200 V until the bromophenol blue dye reached the bottom of the gel. The running buffer (25 mM Tris, 0.2 M glycin, 0.1 % SDS) was cooled externally to 16°C. \nGels/proteins were fixed overnight in 30 % ethanol, 2 % phosphoric acid, washed 3 x 20 min. with 2 % phosphoric acid. The gels were equilibrated with 15 % ammoniumsulfate, 18 % ethanol, 2 % phosphoric acid for 15 min and finally stained with colloidal coomassie blue for 48 h. Gel scanning and image analysis After staining, gels were washed 10 min with pure water and scanned on a Molecular FX Scanner Bio-Rad at 100 µm resolution. Protein spots were imaged first automatically and then manually and analyzed using the PDQuest ™ software Bio-Rad. The normalization was carried out in total density in gel mode according to the manufactures recommendations. For reproducibility, two experiments were performed, each time running 4-control and 6-tumor samples for a total of 20 gels. From them, 14 gels were chosen and used for spot excision and MS analysis. The gels with higher number of spots were selected; all spots (about 180 spots per gel) were excised for MS analysis MALDI-MS A total of 2500 spots from 14 gels were excised using the spot cutter of Bio-Rad and placed into 96-well microtiter plates. Excised gel spots were washed with 20 µL of water for 10 min. and destained twice with 15 µL ammonium bicarbonate 50 mM for 5 min. first and then with 15 µL 50 % ammonium bicarbonate 50 mM - 50 % acetonitrile for 5 min. Finally, gel particles were covered by acetonitrile until gel pieces shrunk and left dry for 10 min. Gels/proteins were digested in situ with 4 µL of ammonium bicarbonate 50 mM containing 20 ng trypsin (Sequencing Grade Modified Trypsin Promega). After 15 min. each gel peace was re-swelled with 10 µL of ammonium bicarbonate 50 mM and incubated for 4 h at 37°C. After 4 h the reaction was stopped by adding 10 µL of trifluoro acetic acid 1 % containing 1.5 % (w/v) n-octyl-β-D-glucopyranoside (OGP) (AppliChem). For the application of the samples, 4 µL of peptide solution were loaded on a MTP Anchor Chip Target 600/384 (Bruker Daltonics) previously prepared with a saturated solution of matrix, α-cyano-4-hydroxy-cinnamic acid (α-HCCA) (Bruker Daltonics). An external calibration was performed by spotting on the 96 calibration positions of the Anchor Chip Target 1 µL of peptide calibration standards (Bruker Daltonics) containing the following peptides: angiotensin II (1046.5420 Da), angiotensin I (1296.6853 Da), substance P (1347.7361 Da), bombesin (1619.8230 Da), ACTH clip 1-17 (2093.0868 Da), ACTH clip 18-39 (2465.1990 Da), somatostatin 28 (3147.4714 Da) and OGP 1.5 % (w/v). Samples were analyzed in a MALDI-TOFFTOF spectrometer (Ultraflex, Bruker Daltonics) using an accelerating voltage of 25 kV for the Peptide Mass Fingerprint (PMF) mode. Peptide matching and protein searches were performed automatically with the MASCOT 2.0 software. For the PMF search the parameters were the following: C-carbaimidomethyl (fixed modification), M-oxidation (variable modification), monoisotopic (mass value), 100 ppm (peptide mass tolerance), 1 (max missed cleavege), mammalia (taxonomy). Five matching peptides and at least 10 % peptide coverage of the theoretical sequences was the minimal requirement for an identity assignment. The identified proteins were organized with the ProteinScape ™ database (Protagen-Bruker Daltonics), checked individually and only mouse proteins or highly homologous sequences from other species were considered. In conclusion, the EGF receptor plays an important role in various tumor diseases. Its hyperactivity can cause cancer of numerous organs. By detecting early stages of tumor growth a dramatic reduction in the mortality rate of cancer patients can be achieved. To date, though, diagnostic markers for liver cancer, such as alpha-Fetoprotein (AFP) and the Des-Gamma-Carboxyprothrombin (DCP) are insufficient for the definite diagnosis of tumor disease. The studies according to the invention provide new information on the role of EGF in tumorigenesis. The serum proteomics facilitates the discovery of biomarkers and enables an improved early detection of cancers and therapeutic monitoring in the various treatment strategies. An EGF-transgenic mouse model has been developed and by using this model the consequences of a changed EGF-signalling in the emergence of liver cancer has been investigated. The mouse model is very similar to the human hepatocellular carcinoma allowing research on the various stages of cancerogenesis. With the help of genomic platform technologies molecular events referring to the individual stages of tumor development could be investigated. Also, the analyses of tumor specific proteins and serum proteins according to the invention provided beneficial approaches for identifying potential serum biomarkers of liver tumors. Blood proteins are easily accessible. Therefore, great efforts are undertaken worldwide to seek serum biomarkers for monitoring the course of disease in patients. Changes in the expression of serum-proteins or -peptides are easy to measure even in the early stages of the disease to measure, well in advance before the disease phenotype associated with significant metabolic damage manifests. A major drawback in serum proteome analytics is, however, the complexity of the sample to be analyzed. For this reason, several additional methods for removing abundant proteins, such as albumin, have been developed to facilitate an identification of the less prevalent and disease associated proteins. However, the pre-treatment of serum samples is problematic, since proteins that only occur in small quantities are lost. Moreover, the prefractioning of serum proteins is costly in terms of time. Here, the efforts for analyzing the serum proteome while avoiding an pre-fractioning are described. The EGF2B-transgenic mouse has already been described in a previous publication. For the serum proteome analysis blood serum was obtained both from wild type mice as well as tumor mice. By using a lysis buffer containing thiourea the serum proteins were extracted and separated by 2D-gelelektrophoresis (2-DE) with the use of two different pH-gradients (3-10, 4-7). Subsequently to colloidal Coomassie-blue staining the spots were cut from the 2D-gel with a spot cutter. Then, the gel samples were washed, discolored and digested with trypsin. An over-expression of EGF in transgenic mice was confirmed by RT-PCR. As previously described in detail, HCC-disease was induced by liver specific overexpression of EGF. In the genomic studies, also signal proteins regulated by an excessive EGF-tyrosine kinase activity could be identified. \nUsing genome wide gene expression analysis, new candidate genes that play a role in tumor formation were identified. Some were changed depending on the degree of differentiation of the tumor, so for example the expression of TGFα and PDGFα. Increased expression of eps-15, a substrate of the EGFR was likewise observed. In less differentiated tumors, the activation of the RhoC-kinase was particularly pronounced. In all of the tumors the expression of cell cycle-regulating proteins such as junB, c-fos, egr-1, and the survival factor IGFBP1 was significantly increased. The oncogenomic studies revealed important information about the serum proteome analyses and were affected by the motivation to find new diagnostic biomarkers for HCC. For overcoming the technical difficulties, the analysis of the serum proteome had to be improved so that as many proteins as possible could be identified after separation with high-resolution 2-DE by mass spectrometric methods (MALDI-MS) . With the help of differential display, tumor-associated serum proteins were discovered in the 2D-gel electrophoresis. In addition, it was possible to automate the MS-analysis of the trypsin-digested proteins. The different behavior of matrix peptide mixtures in peptide mass fingerprinting has already been published in numerous studies. It was further a goal to automate the MS and MS / MS-analyses in order to detect tumor serum proteins in a high-throughput format. For example, with the help of this method the zinc-alpha-2-Glycoprotein could be identified with an outstanding sequence coverage. This was achieved by the use of α-cyano-4-hydroxycinnamic acid in matrix preparations. In addition, this improved mass spectroscopic method also allows access to information on posttranslational modifications such as phosphorylation and glycosylation. \nWith the help of this newly developed protocol, a reference list of the serum-proteome was created, which enables an important basis for studies in healthy and tumor diseased subjects. Figure captions Figure 1 . A: Western blot representing the overexpression of EGF in livers of transgenic mouse model of HCC. (T= tumor samples; C= control samples). B: Histopathology of advanced liver cancer. C: Histopathology of control liver. Figure 2 . A: Example for a map of the mouse serum proteome. (pH 3-10 NL; stain: coomassie blue; loaded sample: 500 µg); B, C: Zoom in for control and tumour serum samples, respectively. Immunoglobulins (circle) and glutathione peroxidase 3 (small rectangle) are down regulated in HCC-mice sera (right side of the panel). Two spots of serum amyloid component P (big rectangle) are up regulated (right side of the panel). Figure 3 . ppm values of the 25 regulated proteins. A: down regulated proteins; C, E: up regulated proteins; B, D, F: proteins virtually present only in tumor samples; G: proteins virtually present only in control samples. Figure 4 . Western blots of fibrinogen gamma (A), apoM (B), alfafetoprotein (C) and serum amyloid component P (D).All these proteins were up-regulated in serum samples of tumor bearing mice. (C= control , T= tumor). Table 1. List of the 25 differentially regulated proteins. Proteins are sorted according to their name. NCBI accession number, MASCOT score, percent of sequence coverage and number of identified peptides (Match) are given. Protein function, p-value, mean fold change and frequency of in gel identification are also reported in table 1. ° Spots were present in 2 gels, but only 1 spot was cut and analyzed for MALDI mass spectrometry identification. * Isoform Supplementary material 1 ( Fig. 5 ): Outline of the experiments. Two experiments were carried out. In the experiment 1, n=1 control serum (non transgenic mouse) (C1) was run in duplicate and then studied for the search and identification of proteins; n = 3 tumour (T1, T2, T3) sera of bearing mice (EGF) were run in duplicate and then studied for the search and identification of proteins. \nIn the experiment 2, n= 4 control sera (non transgenic mice) (C1, C2, C3, C4) and n= 4 tumour sera (T1, T4, T5, T6) were run and then processed for protein identification. In summary a total of 5 gels were studied for the control samples (grey boxes) and a total of 9 gels (grey boxes) were studied for the tumour samples. (IEF: isoelectric focusing ; 2-DE: two dimensional electrophoresis Supplementary material 2 (Fig. 6): Distribution of relative volumes of identified proteins. \nPrimary hepatocellular carcinoma (HCC) is worldwide a common neoplasm with approximately 600 000 death per year. Early detection of tumor growth is essential for therapy and overall survival. Disease-associated proteins have been searched in the sera of HCC bearing mice, which specifically developed HCC, as a result of targeted overexpression of epidermal growth factor (EGF). The picture depicts the distribution of the relative volumes of the spots in the quantification of the 2-DE gels Supplementary material 3 (Fig. 7) The six spots of Apo A-I in 2-D gels. Supplementary material 4 (Fig. 8) The five spots of Apo H in 2-D gels. Supplementary material 5 (Fig. 9) Overexpression and ppm values of apolipoprotein E (apo E) in sera of HCC mice. R = ppm ratio (tumour / control). Supplementary material 6 (Fig. 10): Overexpression and ppm values of apolipoprotein M (apo M) in sera of HCC mice. R = ppm ratio (tumour / control). Supplementary material 7 (Fig. 11): Overexpression and ppm values of serum amyloid component P (SAP). (A, B): control samples. (D, E): sera of HCC mice, the second SAP isoform, SAP*, is identified in sera of HCC mice only. (C, F): 3-D view of SAP spots in control and HCC mice respectively. R = ppm ratio (tumour / control). Supplementary material 8 (Fig. 12) Overexpression and ppm values of two A2MG-fragments in sera of HCC mice (E, F, G, H). The x and y isoforms (A, E). R = ppm ratio (tumour / control). Supplementary material 9 (Fig. 13): Down-regulation of glutathione peroxidase 3 (Gpx3). (A, C): control samples, gpx3 is present in two isoforms, Gpx3* and Gpx3. (B, D): tumour samples, the isoform Gpx3 is down regulated, while the isoform Gpx3* is now virtually absent. Supplementary material 10 (Fig. 14): (A): Expression of fibrinogens alpha, beta and gamma (Fga, Fgb, Fgg) in sera of HCC mice. (B, C, D): zoom view of the gels; Not all tumor animals carried the three fibrinogens in sera. Supplementary material 11 (Fig. 15): Down regulation of immunoglobulins. Many immunoglobulins were virtually absent in tumor samples (B). Supplementary table 1. Serum proteins A total of 2500 spots derived from 14 gels were excised and digested with trypsin (Promega). Peptides were loaded on a MTP Anchor Chip Target 600/384 (Bruker Daltonics) previously prepared with HCCA and analyzed in a MALDI-TOF-TOF spectrometer (Ultraflex I, Bruker Daltonics). Peptide matching and protein searches were performed automatically with the MASCOT 2.0 software. MASCOT scores are also reported in the table (see column \"Mascot Score\"). Five matching peptides (see column \"N° of matched peptides\") and at least 10 % peptide coverage of the theoretical sequences was the minimal requirement for an identity assignment (see column \"Coverage\"). The identified proteins were organized with the ProteinScape ™ database (Bruker Daltonics) and checked individually. \nIn the table proteins are sorted by alphabetical order in the second column and the NCBI annotation is given in the first column. The theoretical pl, MW, and biological function are given herein. Expression of proteins and frequency of identification are reported in the column \"regulation\" and \"gels\" respectively. Supplementary table 2. Sequences of the identified peptides.\n TABLE-tabl0001 Table 1 Acc. Number (NCBI) Protein Name Mascot Score Sequence Covera ge % N° of matched peptides Function p- value Regulation (tumor / kontrol) Gels gi|191765 Alpha fetoprotein 234 39,2 16 Unknown 0,035 1,6 3 gi|14318646 Amylase 1, salivary 72,5 23,1 13 Unknown - tumor 3 gi|6753096 Apolipoprotein A-I 84,2 32,3 20 Reverse transport of cholesterol from tissues to the liver - tumor 4 gi|6753102 Apolipoprotein E 220 60,5 18 Binding and transport 0,035 2,2 12 gi|9055162 Apolipoprotein M 114 45,3 9 Lipid transport. 0,044 8 8 gi|2921308 Carboxyl esterase precursor 93,3 26,4 14 Metabolism of xenobiotics - tumor 2 gi|13899173 Caspase recruitment domain protein 12 70,3 11,7 9 Promotion of apoptosis. - tumor 2 gi|49523333 Clusterin (Apolipoprotein J) 79,6 22,1 10 Maybe binding to cells, membranes and hydrophobic proteins. - tumor 4 gi|33563252 Fibrinogen, alpha polypeptide 204 47,2 26 Cofactor in platelet aggregation - tumor 1° gi|33859809 Fibrinogen, beta polypeptide 263 59,9 29 Cofactor in platelet aggregation - tumor 1° gi|19527078 Fibrinogen, gamma polypeptide 234 60,6 22 Cofactor in platelet aggregation - tumor 1° gi|52843238 Glutathione peroxidase 3 117 43 9 Unknown 0,002 0,2 4 gi|40715898 HMW-kininogen-II variant 106 25,5 9 Unknown - control 2 gi|21594125 Lifr protein 95,5 20,4 10 Unknown - control 3 gi|8569601 Major urinary protein 1 161 73,5 11 Binds pheromones 0,22 0,14 3 gi|6754654 Mannose binding lectin (A) 113 45,6 10 Binds mannose and N-acetylglucosamine in a Ca++ dependent way - control 5 gi|233018 Mannose-binding protein C; MBP-C 160 49,6 13 Unknown - control 3 gi|387437 MHC factor B 246 58,5 30 . Complement system - tumor 4 gi|6679182 Orosomucoid 1 100 34,8 10 Acute-phase reaction - control 4 gi|53787 Properdin (AA 5 - 441) 143 32,5 16 . Complement system. 0,103 6 0,4 6 gi|34785996 A2MG 216 22,3 22 Endopeptidase inhibitor. 0,001 8 1,8 14 gi|34785996 A2MG * 216 22,3 22 . Endopeptidase inhibitor. 2,6 e-5 3,2 14 gi|6679383 Serine (or cysteine) proteinase inhibitor, clade F, member 2; plasmin inhibitor alpha 2; alpha 2 antiplasmin; serine (or cysteine) proteinase inhibitor, clade F (alpha-2 antiplasmin, pigment epithelium derived factor), member 2 [Mus musculus] 124 35 17 Inhibitor for plasmin, trypsin, and chymotrypsin 0,303 3 4,7 5 gi|38174334 Serum amyloid P-component 122 37,5 9 Unknown 0,010 3 10 7 gi|38174334 Serum amyloid P-component * 92,3 27,2 7 Unknown - tumor 4 \n TABLE-tabl0002 SUPPLEMENTARY TABLE 1 Acc. Number (NCBI) Protein Name pl Mr (kDa) Mascot Score Sequence Coverage % N° of matched peptides Function Regulation (tumor / control) Gels gi|15277503 ACTB protein 5,5 40,2 249 61,4 20 Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells 2 gi|71621 Actin beta 5,2 41,6 192 65,2 19 Involved in various types of cell motility. 1 gi|21553101 Afamin 5,5 69,6 146 38,1 18 Transport 5 gi|20072386 Afm protein 5,6 47,6 186 50,4 20 Transport 11 gi|11277085 Albumin (fragment) 5,4 51,4 283 56,7 22 Serum albumin, the main protein of plasma, has a good binding capacity for water, Ca(2+), Na(+), K(+), fatty acids, hormones, bilirubin and drugs. Its main function is the regulation of the colloidal osmotic pressure of blood 13 gi|33859506 Albumin 1 5,7 68,7 421 65,6 37 Transport 14 gi|42542817 Alpha fetoprotein 5,6 67,3 111 43 18 Unknown up regulated 3 gi|191765 Alpha fetoprotein 5,4 47,2 234 39,2 16 Unknown up regulated 9 gi|191844 Alpha-1 protease inhibitor 2 5,3 44,8 166 60,4 19 Inhibitor of serine proteases. Its primary target is elastase, but it also has a moderate affinity for plasmin and thrombin. 7 gi|31982171 Alpha-2 macroglobulin MUG1 6 165,1 131 22,6 31 A proteinase activates the inhibitor by specific proteolysis in the bait region, which, by an unknown mechanism leads to reaction at the cysteinyl-glutamyl internal thiol ester site and to a conformational change, whereby the proteinase is trapped and/or covalently bound to the inhibitor. 9 While in the tetrameric proteinase inhibitors steric inhibition is sufficiently strong, monomeric forms need a covalent linkage between the activated glutamyl residue of the original thiol ester and a terminal amino group of a lysine or another nucleophilic group on the proteinase, for inhibition to be effective gi|7304875 Alpha-2-HS-glycoprotein (Fetuin) 6,1 37,3 98,8 48,4 13 Probably involved in differentiation. 8 gi|14318646 Amylase 1, salivary 6,6 57,6 72,5 23,1 13 Unknown tumor 3 gi|425520 Anti-colorectal carcinoma light chain 6,2 26,5 88,8 40,7 6 Unknown 1 gi|26345182 Apolipoprotein A1 (Unnamed protein product) 5,4 30,6 163 62,5 18 Participates in the reverse transport of cholesterol from tissues to the liver for excretion by promoting cholesterol efflux from tissues and by acting as a cofactor for the lecithin cholesterol acyltransferase (LCAT). 12 gi|14789706 Apolipoprotein A4 5,3 45 292 73,9 25 May have a role in chylomicrons and VLDL secretion and catabolism. Required for efficient activation of lipoprotein lipase by ApoC-II; potent activator of LCAT. Apoa-IV is a major component of HDL and chylomicrons. 10 gi|6753096 Apolipoprotein A-I 5,4 30,5 84,2 32,3 20 Participates in the reverse transport of cholesterol from tissues to the liver for excretion by promoting cholesterol efflux from tissues and by acting as a cofactor for the lecithin cholesterol acyltransferase (LCAT). tumor 4 gi|6753102 Apolipoprotein E 5,7 33,2 220 60,5 18 Mediates the binding, internalization, and catabolism of lipoprotein particles. It can serve as a ligand for the LDL (apo B/E) receptor and for the specific apo-E receptor (chylomicron remnant) of hepatic tissues. up regulated 12 gi|1938223 Apolipoprotein H (beta-2 glycoprotein I ) 9,7 36,3 153 59,1 15 Binds to various kinds of negatively charged substances such as heparin, phospholipids, and dextran sulfate. May prevent activation of the intrinsic blood coagulation cascade by binding to phospholipids on the surface of damaged cells. 12 gi|9055162 Apolipoprotein M 6,1 21,3 114 45,3 9 Probably involved in lipid transport. up regulated 8 gi|2921308 Carboxylesterase precursor 5 61,1 93,3 26,4 13 Involved in the detoxification of xenobiotics and in the activation of ester and amide prodrugs. Involved in the extracellular metabolism of lung surfactant tumor 2 gi|13899173 Caspase recruitment domain protein 12 6,27 116,1 70,3 11,7 9 Plays a role in the promotion of apoptosis tumor 2 gi|49523333 Clusterin (Apolipoprotein J) 5,4 51,7 79,6 22,1 10 Not yet clear. It is known to be expressed in a variety of tissues and it seems to be able to bind to cells, membranes and hydrophobic proteins. It has been associated with programmed cell death. tumor 4 gi|6753798 Coagulation factor II (prothrombin) 6 70,3 215 45 24 Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. 10 gi|13624321 Coagulation factor XIII, beta subunit 6,6 76 190 32,8 19 The B chain of factor XIII is not catalytically active, but is thought to stabilize the A subunits and regulate the rate of transglutaminase formation by thrombin. 3 gi|6996919 Complememnt histocompatibility 2, complement component factor B 7,1 85 264 52 30 Cell proliferation and complement activation, alternative pathway. 12 gi|28175786 Complement C3 precursor (HSE-MSF) 6,4 186,4 289 29 40 C3 plays a central role in the activation of the complement system. Its processing by C3 convertase is the central reaction in both classical and alternative complement pathways. After activation C3b can bind covalently, via its reactive thiolester, to cell surface carbohydrates or immune aggregates. 12 gi|220349 Complement C4 9,1 59,2 217 47,9 22 C4 plays a central role in the activation of the classical pathway of the complement system. It is processed by activated C1 which remove from the alpha chain the C4a anaphylatoxin. 8 gi|309119 Complement C4b-binding protein precursor 6 46,6 93,9 33,8 11 Controls the pathway of complement activation. It accelerates the degradation of the C4bC2a complex. It interacts with SAP 1 gi|15030019 Complement component 6 5,7 86,6 207 39 27 Involved in the formation of the lytic c5b-9m complex 2 gi|27462724 Complement component C1SA 4,8 76,9 72,3 18,3 9 C1s B chain is a serine protease that combines with C1q and C1s to form C1, the first component of the classical pathway of the complement system. C1r activates C1 s so that it can, in turn, activate C2 and C4 1 gi|19072788 Complement component factor h 6,6 139 264 32 30 Factor H functions as a cofactor in the inactivation of C3b by factor I and also increases the rate of dissociation of the C3bBb complex (C3 convertase) and the (C3b)NBB complex (C5 convertase) in the alternative complement pathway 10 gi|6671744 Complement component factor i 9,2 67,2 87,6 21,7 7 Responsible for cleaving the alpha chains of C4b and C3b in the presence of the cofactors C4 binding protein and factor H respectively. 6 gi|9954973 Complement D Chain D, N-Terminally Truncated C3dg Fragment 5 31,1 75,1 38,3 10 C3 plays a central role in the activation of the complement system. Its processing by C3 convertase is the central reaction in both classical and alternative complement pathways. After activation C3b can bind covalently, via its reactive thiolester, to cell surface carbohydrates or immune aggregates. Derived from proteolytic degradation of 1 complement C3, C3a anaphylatoxin is a mediator of local inflammatory process. It induces the contraction of smooth muscle, increases vascular permeability and causes histamine release from mast cells and basophilic leukocytes. The short isoform has B-cell stimulatory activity. gi|6754132 Complement histocompatibility 2, Q region locus 10 5,1 37,3 217 53,2 18 Involved in the presentation of foreign antigens to the immune system 9 gi|54173 Contraspin 5 46,7 259 60,5 22 Contrapsin inhibits trypsin-like proteases 6 gi|38614350 Cp protein 5,5 121,1 248 40,5 36 Ceruloplasmin is a blue, copper binding (6-7 atoms per molecule) glycoprotein found in plasma. Four possible functions are ferroxidase activity, amine oxidase activity, copper transport and homeostasis, and superoxide dismutase activity. 13 gi|19388017 Cpn2 protein 5,5 62 112 29,7 11 The 83 kDa subunit binds and stabilizes the catalytic subunit at 37 degrees Celsius and keeps it in circulation. Under some circumstances it may be an allosteric modifier of the catalytic subunit 5 gi|11055360 Epidermal growth factor receptor isoform 2 6,8 71,4 239 43,4 22 cell proliferation - cellular morphogenesis -epidermal growth factor receptor signaling pathway positive regulation of cell proliferation - protein amino acid autophosphorylation - regulation of peptidyl-tyrosine phosphorylation signal transduction 9 gi|6679689 Esterase 1 4,9 61,1 164 46,8 18 Involved in the detoxification of xenobiotics and in the activation of ester and amide prodrugs. Involved in the extracellular metabolism of lung surfactant 9 gi|33563252 Fibrinogen, alpha polypeptide 7 61,3 204 47,2 26 Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation tumor 1° gi|33859809 Fibrinogen, beta polypeptide 6,5 54,8 263 59,9 29 Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation tumor 1° gi|19527078 Fibrinogen, gamma polypeptide 5,5 49,4 234 60,6 22 Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation tumor 1° gi|1181242 Fibronectin 5,2 160,9 161 23,5 25 Fibronectins bind cell surfaces and compounds including collagen, fibrin, heparin, DNA, and actin. They are involved in cell adhesion, cell motility, opsonization, wound healing, and maintenance of cell shape. Interaction with TNR mediates inhibition of cell adhesion and neurite outgrowth. 5 gi|46849812 Fibronectin 1 5,4 272,5 349 31 59 Fibronectins bind cell surfaces and various compounds including collagen, fibrin, heparin, DNA, and actin. Fibronectins are involved in cell adhesion, cell motility, opsonization, wound healing, and maintenance of cell shape. Interaction with TNR mediates inhibition of cell adhesion and neurite outgrowth. 9 gi|28916693 Gelsolin 5,8 85,9 255 47,6 28 Calcium-regulated, actin modulating protein that binds to the plus (or barbed) ends of actin monomers or filaments, preventing monomer exchange (end-blocking or capping). It can promote the assembly of monomers into filaments (nucleation) as well as sever filaments already formed. 12 gi|52843238 Glutathione peroxidase 3 9,1 25,4 117 43 9 Unknown down regulated 4 gi|17512357 Gpld1 protein 6,3 93,6 125 19,4 16 This protein hydrolyzes the inositol phosphate linkage in proteins anchored by phosphatidylinositol glycans (GPI-anchor) thus releasing these proteins from the membrane. 3 gi|1694789 GRS protein 5,3 20,1 70 44,6 5 Retards apoptosis induced by IL-3 deprivation. May function in the response of hemopoietic cells to external signals and in maintaining endothelial survival during infection 1 gi|37719755 GUGU alpha 6,2 44,4 155 50,6 16 Multifunction 3 gi|23956086 Hemopexin 9 51,3 238 55,7 23 Binds heme and transports it to the liver for breakdown and iron recovery, after which the free hemopexin returns to the circulation 11 gi|50082914 High molecular weight kininogen I isoform DeltaD5 4,7 53,2 89,2 27,7 11 (1) Kininogens are inhibitors of thiol proteases; 3 (2) HMW-kininogen plays an important role in blood coagulation by helping to position optimally prekallikrein and factor XI next to factor XII; ; (3) HMW kininogen inhibits the thrombin- and plasmin-induced aggregation of thrombocytes; (4) the active peptide bradykinin that is released from HMW-kininogen shows a variety of physiological effects: (4A) influence in smooth muscle contraction, (4B) induction of hypotension, (4C) natriuresis and diuresis, (4D) decrease in blood glucose level, (4E) it is a mediator of inflammation and causes (4E1) increase in vascular permeability, (4E2) stimulation of nociceptors (4E3) release of other mediators of inflammation (e.g. prostaglandins), (4F) it has a cardioprotective effect (directly via bradykinin action, indirectly via endothelium-derived relaxing factor action) (5) LMW kininogen inhibits the aggregation of thrombocytes; (6) LMW kininogen is in contrast to HMW kininogen not involved in blood clotting gi|40715898 HMW-kininogen-II variant 6 51 86,4 25,8 12 (1) Kininogens are inhibitors of thiol proteases; control 2 (2) HMW-kininogen plays an important role in blood coagulation by helping to position optimally prekallikrein and factor XI next to factor XII; (3) HMW kininogen inhibits the thrombin- and plasmin-induced aggregation of thrombocytes; (4) the active peptide bradykinin that is released from HMW-kininogen shows a variety of physiological effects: (4A) influence in smooth muscle contraction, (4B) induction of hypotension, (4C) natriuresis and diuresis, (4D) decrease in blood glucose level, (4E) it is a mediator of inflammation and causes (4E1) increase in vascular permeability, (4E2) stimulation of nociceptors (4E3) release of other mediators of inflammation (e.g. prostaglandins), (4F) it has a cardioprotective effect (directly via bradykinin action, indirectly via endothelium-derived relaxing factor action); (5) LMW kininogen inhibits the aggregation of thrombocytes; (6) LMW kininogen is in contrast to HMW kininogen not involved in blood clotting gi|31615671 Ig (A Chain A, Crystal Structure Of Fab Fragment Of Antibody Hyhel-26 Complexed With Lysozyme) 5,5 23,6 76,4 44,4 6 Host defense control 3 gi|4930001 Ig (A Chain A, Idiotope-Anti Idiotope Fab-Fab Complex) 6 23,7 65,8 41,6 7 Host defense control 4 gi|11514687 Ig (A Chain A, Lyme Disease Antigen Ospa In Complex With Neutralizing Antibody Fab La-2) 7,4 23,6 78,7 49,3 6 Host defense control 1 gi|42543442 Ig (A Chain A, S25-2- Kdo Monosaccharide Complex) 9,4 24,2 89,2 44,7 7 Host defense control 2 gi|7766934 Ig (A Chain A, Structure Of An Activity Suppressing Fab Fragment To Cytochrome P450 Aromatase) 6 23,8 78,2 42,9 6 Host defense control 1 gi|27373551 Ig (antibody variable domain) 7 12,7 68,5 48,7 5 Host defense tumor 1 gi|1870378 Ig (Anti-DNA immunoglobulin light chain IgG) 6,3 11,6 109 57 6 Host defense up regulated 5 gi|12002896 Ig (anti-human apolipoprotein A monoclonal antibody mAb(a)23L kappa light chain) 7,4 23,5 82,4 44,6 7 Host defense control 1 gi|349893 Ig (C Chain C, Fab (Igg2a,Kappa) Fragment (26-10) Complex With Digoxin) 7,8 24 114 47,5 8 Host defense control 1 gi|47059057 Ig (gamma-2b-immunoglobulin) 8,9 51,9 69 29 8 Host defense tumor 2 gi|1806128 Ig (immunoglobulin constant heavy chain) 9,3 51,7 88,4 41,9 12 Host defense 5 gi|10121892 Ig (immunoglobulin IgM MP 18-3-117 kappa light chain) 5,2 26 76,9 42,1 7 Host defense control 3 gi|196723 Ig (immunoglobulin kappa chain VK-1) 5,6 10,9 125 61,6 7 Host defense control 2 gi|18033701 Ig (immunoglobulin light chain constant region) 5,5 11,3 65,6 70,2 5 Host defense control 1 gi|13399686 Ig (L Chain L, 64m-2 Antibody Fab Complexed With D(5ht)(6-4)t) 6 23,9 115 70,5 10 Host defense control 5 gi|3212470 Ig (L Chain L, Anti Taq Fab Tp7) 5,7 23,1 104 58,6 5 Host defense control 2 gi|5542523 Ig (L Chain L, Bactericidal Antibody Against Neisseria Meningitidis) 9,3 24,1 107 66,2 11 Host defense control 2 gi|16975338 Ig (L Chain L, Crystal Structure Of Immunoglobulin Fab Fragment Complexed With 17-Beta-Estradiol) 6,6 23,6 102 69,2 11 Host defense control 2 gi|18655521 Ig (L Chain L, Crystal Structure Of The Fab Fragment Of The Mouse Anti- Human Fas Antibody Hfe7a) 4,8 23,9 81,1 56,4 8 Host defense 2 gi|1942810 Ig (L Chain L, Fab Fragment Of A Neutralizing Antibody Directed Against An Epitope Of Gp41 From Hiv-1) 6,4 24,2 124 80 12 Host defense control 2 gi|7546516 Ig (L Chain L, Fab Fragment Of Neutralising Monoclonal Antibody 4c4 Complexed With G-H Loop From Fmdv) 5,6 23,7 72,4 37 5 Host defense control 1 gi|17943084 Ig (L Chain L, Structural Basis For Disfavored Elimination Reaction In Catalytic Antibody 1d4) 7,8 24,2 118 59,1 8 Host defense control 2 gi|2624743 Ig (L Chain L, Structure Of A Catalytic Antibody, Igg2a Fab Fragment) 7,3 24 69,9 45,7 8 Host defense control 1 gi|32263981 Ig (mAb immunoglobulin light chain variable region) 9,9 11,6 80,9 59,8 7 Host defense control 1 gi|18568342 Ig (monoclonal antibody BBK-2 light chain) 6,5 26,1 77,8 51,7 8 Host defense control 1 gi|52382 Ig (mu(b) immunoglobulin heavy chain) 6,4 50 153 40,7 19 Host defense control 1 gi|7439167 Ig (PC4436 monoclonal antibody 13-1 heavy chain) 8,7 49,3 92,6 29,1 8 Host defense 2 gi|15824610 Ig (Pterin-mimicking anti-idiotope kappa chain variable region) 7,8 12 75,4 77,5 5 Unknown control 1 gi|780265 Ig gamma-1 chain C region (15C5) (fragment) 9 17,3 70,5 38,8 8 Host defense 3 gi|1799551 Ig gamma-chain, secrete type 9,4 36,2 88,5 31 9 Host defense 1 gi|223428 Ig H-C allotype gamma2b 7,8 36,6 174 56 19 Host defense 9 gi|224008 Ig J chain 4,4 15,8 111 42,4 9 Host defense control 2 gi|12832551 Ig K (unnamed protein product) 6,4 23,2 98 43,1 8 Host defense control 2 gi|896077 Ig kappa chain 7,6 8,7 90,1 74,7 6 Host defense control 3 gi|896089 Ig kappa chain 9,5 10,5 82 82,3 6 Host defense control 1 gi|896103 Ig kappa chain 4,3 10,3 64,7 57,9 5 Host defense control 3 gi|896107 Ig kappa chain 4,6 9,1 71,6 71,8 5 Host defense control 1 gi|7513693 Ig kappa chain (Mab03-1) 6,4 23,6 104 58,9 11 Host defense control 1 gi|110429 Ig kappa chain V region (9.42 9,1 10,4 73,4 58,5 6 Host defense control 1 gi|49258884 Ig kappa chain V region (D444) 9,3 11,8 70,1 50,9 7 Host defense control 3 gi|930226 Ig kappa chain V region (hybridoma NC19-E11) 5,1 11 90 55,6 8 Host defense control 2 gi|125796 Ig kappa chain V-III region PC 2880/PC 1229 5,2 12 73,7 66,7 6 Host defense down regulated 1 gi|197064 Ig kappa chain V-region (V-Jk1) protein 7,3 11,9 92,3 99,1 7 Host defense control 1 gi|1613779 Ig kappa light chain 5,5 23,9 69,6 38,3 10 Host defense control 1 gi|284924 Ig light chain V region (clone 185-c1) 6,1 10,7 86,9 75,5 6 Host defense tumor 1 gi|494164 Igg2a Fab Fragment (Fab 179) 5,7 23,9 65,7 39,6 5 Host defense control 1 gi|229901 Igg2b, Kappa 5,8 23,7 108 70,1 12 Host defense control 5 gi|62204734 Inter alpha-trypsin inhibitor, heavy chain 4 6,1 104 220 37 29 Unknown 5 gi|16418335 Leucine-rich alpha-2-glycoprotein 6 37,4 71 23,4 8 Unknown 3 gi|21594125 Lifr protein (leukemia inhibitory factor receptor) 6,5 81,3 95,5 20,4 10 The WSXWS motif appears to be necessary for proper protein folding and thereby efficient intracellular transport and cell-surface receptor binding control 3 gi|8569601 Major urinary protein 1 4,9 20,6 161 73,5 11 Binds pheromones down regulated 3 gi|6754654 Mannose binding lectin (A) 7,3 25,4 113 45,6 10 Binds mannose and N-acetylglucosamine in a Ca++ dependent way. Is capable of host defense against pathogens, by activating the classical complement pathway independently of the antibody control 5 gi|233018 Mannose binding protein C 4,9 25,9 160 49,6 11 Binds mannose and N-acetylglucosamine. Host defense against pathogens, by activating the complement pathway independently of the antibody. control 3 gi|2118830 MHC class I histocompatibility antigen H-2 Q10 alpha chain 5,1 37 240 53,7 21 Involved in the presentation of foreign antigens to the immune system 9 gi|387437 MHC factor B 8,7 54 246 58,5 30 Factor B which is part of the alternate pathway of the complement system is cleaved by factor D into 2 fragments: Ba and Bb. Bb, a serine protease, then combines with complement factor 3b to generate the C3 or C5 convertase tumor 4 gi|55217 Murine valosin-containing protein 5,1 89,3 91,6 19,1 12 Necessary for the fragmentation of Golgi stacks during mitosis and for their reassembly after mitosis. Involved in the formation of the transitional endoplasmic reticulum (tER). The transfer of membranes from the endoplasmic reticulum to the Golgi apparatus occurs via 50-70 nm transition vesicles which derive from part-rough, part-smooth transitional elements of the endoplasmic reticulum (tER). 1 Vesicle budding from the tER is an ATP-dependent process. The ternary complex containing UFD1 L, VCP and NPL4 binds ubiquitinated proteins and is necessary for the export of misfolded proteins from the ER to the cytoplasm, where they are degraded by the proteasome. The NPL4-UFD1L-VCP complex regulates spindle disassembly at the end of mitosis and is necessary for the formation of a closed nuclear envelope gi|6679182 Orosomucoid 1 5,4 23,9 100 34,8 10 Appears to function in modulating the activity of the immune system during the acute-phase reaction control 4 gi|31982113 Plasminogen [Mus musculus] 6,1 90,8 449 61,5 53 Plasmin dissolves the fibrin of blood clots and acts as a proteolytic factor in a variety of other processes including embryonic development, tissue remodeling, tumor invasion, and inflammation; in ovulation it weakens the walls of the Graafian follicle. It activates the urokinase type plasminogen activator, collagenases and several complement zymogens, such as C1 and C5. It cleaves fibrin, fibronectin, thrombospondin, laminin and von Willebrand factor. Its role in tissue remodeling and tumor invasion may be modulated by CSPG4 10 gi|2144495 PLMS plasmin 6 90,8 352 51,4 38 Plasmin dissolves the fibrin of blood clots and acts as a proteolytic factor in a variety of other processes including embryonic development, tissue remodeling, tumor invasion, and inflammation; in ovulation it weakens the walls of the Graafian follicle. It activates the urokinase type plasminogen activator, collagenases and several complement zymogens, such as C1 and C5. It cleaves fibrin, fibronectin, thrombospondin, laminin and von Willebrand factor. Its role in tissue remodeling and tumor invasion may be modulated by CSPG4 n.v.o. 8 gi|6680608 Pregnancy zone protein 6,2 165,8 113 13,7 14 Endopeptidase inhibitor activity 8 gi|53787 Properdin (AA 5 - 441) 8,4 47,5 143 32,5 16 A positive regulator of the alternate pathway of complement. It binds to and stabilizes the C3- and C5 convertase enzyme complexes. up regulated 6 gi|49868 Put. beta-actin (aa 27-375) 5,7 39,2 136 44,4 16 Involved in various types of cell motility. 1 gi|34785996 Pzp protein 6,2 165,9 187 28,2 32 Unknown up regulated 14 gi|33859612 Retinol binding protein 4 5,6 23,2 147 51,7 14 Delivers retinol from the liver stores to the peripheral tissues. In plasma, the RBP-retinol complex interacts with transthyretin, this prevents its loss by filtration through the kidney glomeruli. 9 gi|6678083 Serine (or cysteine) proteinase inhibitor, clade A, member 1 a 5,3 45,9 149 62,7 20 Inhibitor of serine proteases. Can inhibit trypsin and chymotrypsin; relatively ineffective against elastase 6 gi|15029662 Serine (or cysteine) proteinase inhibitor, clade A, member 1 a 5,3 46 143 51,6 17 Inhibitor of serine proteases. Its primary target is elastase, but it also has a moderate affinity for plasmin and thrombin. 8 gi|6678085 Serine (or cysteine) proteinase inhibitor, clade A, member 1d 5,2 46 171 47 14 Inhibitor of serine proteases. Can inhibit trypsin and chymotrypsin; relatively ineffective against elastase 1 gi|6678087 Serine (or cysteine) proteinase inhibitor, clade A, member 1 e 5,4 45,9 154 41,6 19 Does not inhibit elastase or chymotrypsin. No target protease has been identified to date 5 gi|18044689 Serine (or cysteine) proteinase inhibitor, clade A, member 3K 5 46,9 99,1 40 13 serine-type endopeptidase inhibitor activity 1 gi|18252782 Serine (or cysteine) proteinase inhibitor, clade C (antithrombin), member 1 6,1 52 195 61,7 25 Most important serine protease inhibitor in plasma that regulates the blood coagulation cascade. AT-III inhibits thrombin as well as factors IXa, Xa and XIa. Its inhibitory activity is greatly enhanced in the presence of heparin. 7 gi|6679383 Serine (or cysteine) proteinase inhibitor, clade F, member 2 5,8 54,9 106 34,6 17 Serine-type endopeptidase inhibitor activity up regulated 5 gi|15929675 Serpina1a protein 5,4 45,6 219 62 23 Inhibitor of serine proteases. Can inhibit trypsin and chymotrypsin; relatively ineffective against elastase. 12 gi|14602605 Serpina1a protein 5,3 46 224 62 24 Inhibitor of serine proteases. Can inhibit trypsin and chymotrypsin; relatively ineffective against elastase. 7 gi|38174334 Serum amyloid P-component 6,2 26,2 122 37,5 9 Unknown up regulated 7 gi|20330802 Transferrin 6,8 76,7 159 40 47 Transferrins are iron binding transport proteins which can bind two Fe(3+) ions in association with the binding of an anion, usually bicarbonate. It is responsible for the transport of iron from sites of absorption and heme degradation to those of storage and utilization. Serum transferrin may also have a further role in stimulating cell proliferation. 13 gi|19354093 Transthyretin 5,5 15,8 155 96,6 11 Thyroid hormone-binding protein. Probably transports thyroxine from the bloodstream to the brain. 8 gi|111243 Vitamin D-binding protein 5,2 53,1 288 65,3 30 Multifunction 12 gi|1083568 Zinc-alpha 2-glycoprotein 5,7 33,5 94,6 40 10 Stimulates lipid degradation in adipocytes and causes the extensive fat losses associated with some advanced cancers 1 \n TABLE-tabl0003 Supplementary Table 2 NCBI Number Protein Identified Peptides gi|15277503 ACTB protein AGFAGDDAPR AVFPSIVGRPR DLYANTVLSGGTTMYPGIADR DSYVGDEAQSKR GYSFTTTAER GYSFTTTAEREIVR HQGVMVGMGQK ox ox HQGVMVGMGQKDSYVGDEAQSK ox ox IIAPPERK IKIIAPPER ILTERGYSFTTTAER IWHHTFYNELR KDLYANTVLSGGTTMYPGIADR ox LCYVALDFEQEMATAASSSSLEK cam ox LDLAGRDLTDYLMK LDLAGRDLTDYLMK ox QEYDESGPSIVHR QEYDESGPSIVHRK SYELPDGQVITIGNER TTGIVMDSGDGVTHTVPIYEGYALPHAILR ox VAPEEHPVLLTEAPLNPK gi|71621 Actin beta AGFAGDDAPR AVFPSIVGRPR DDDIAALVVDNGSGMCK cam ox DLYANTVLSGGTTMYPGIADR ox DSYVGDEAQSKR EITALAPSTMK ox GYSFTTTAER GYSFTTTAEREIVR HQGVMVGMGQK ox IIAPPERK IKIIAPPER IWHHTFYNELR KDLYANTVLSGGTTMYPGIADR ox LCYVALDFEQEMATAASSSSLEK cam ox LDLAGRDLTDYLMK ox QEYDESGPSIVHR QEYDESGPSIVHRK SYELPDGQVITIGNER TTGIVMDSGDGVTHTVPIYEGYALPHAILR ox VAPEEHPVLLTEAPLNPK gi|21553101 Afamin AAPQLPMEELVSLSK ANVGFLPPFPTLDPEEK SLAMVQQECNQFQELGKDTLQR ox cam CWADNTLPECSK cam cam DRCWADNTLPECSK cam cam DSDPDKFFAEFIYEYSR EACIINANKDDRPEGLSLR cam FTAAREECSEVQEPESCFSPESSK cam cam FTESENVCQER cam HFLVKFTK IGFKDLTTLLEDVSSMYEGCCEGDVVHCIR cam cam cam KANVGFLPPFPTLDPEEK RLCFFYNK cam TINPAVDHCCK cam cam TINPAVDHCCKTDFAFR cam cam VLNSINVAVFSK VMLDYRDR VMLDYRDR ox VYMDFLEDCCSR ox cam cam gi|20072386 Afm protein ANVGFLPPFPTLDPEEK ASSSYQRNVCGALIK cam ATCFQAKAAPITQYLK cam CWADNTLPECSK cam cam DDRPEGLSLREAK DSDPDKFFAEFIYEYSR EACIINANKDDRPEGLSLR cam EAKFTESENVCQER cam FTESENVCQER cam ITKVYMDFLEDCCSR ox cam cam KANVGFLPPFPTLDPEEK LCFFYNKK cam NVCGALIKFGPK cam QFQELGKDTLQR RHPDLSTPELLR SLAMVQQECK ox cam SQSQVVNHICSK cam SQSQVVNHICSKQDSISSK cam VLNSINVAVFSK VMLDYRDR VYMDFLEDCCSR ox cam cam gi|11277085 Albumin (fragment) AETFTFHSDICTLPEKEK cam APQVSTPTLVEAAR CCAEANPPACYGTVLAEFQPLVEEPK cam cam cam CCAEANPPACYGTVLAEFQPLVEEPKNLVKcam cam cam CCSGSLVER cam cam CCTLPEDQRLPCVEDYLSAILNR cam cam cam DVFLGTFLYEYSR ENPTTFMGHYLHEVAR HPDYSVSLLLR LGEYGFQNAILVR LPCVEDYLSAILNR cam LQTCCDKPLLK cam cam LQTCCDKPLLKK cam cam LSQTFPNADFAEITK LSQTFPNADFAEITKLATDLTK NYAEAKDVFLGTFLYEYSR QEPERNECFLQHK cam RHPDYSVSLLLR RPCFSALTVDETYVPK cam TNCDLYEKLGEYGFQNAILVR cam VCLLHEKTPVSEHVTK cam YMCENQATISSK cam YTQKAPQVSTPTLVEAAR gi|33859506 Albumin 1 SEIAHRYNDLGEQHFK AETFTFHSDICTLPEKEK cam AFKAWAVAR AHCLSEVEHDTMPADLPAIAADFVEDQEVCK cam ox cam APQVSTPTLVEAAR APQVSTPTLVEAARNLGR CCAEANPPACYGTVLAEFQPLVEEPK cam cam cam CCSGSLVER cam cam CCTLPEDQR cam cam CCTLPEDQRLPCVEDYLSAILNR cam cam cam DDNPSLPPFERPEAEAMCTSFK ox cam DVFLGTFLYEYSR DVFLGTFLYEYSRR EAHKSEIAHR ECCHGDLLECADDRAELAK cam cam cam EFKAETFTFHSDICTLPEK cam ENPTTFMGHYLHEVAR ox ENYGELADCCTK cam cam HPDYSVSLLLR LCAIPNLRENYGELADCCTK cam cam cam LGEYGFQNAILVR LPCVEDYLSAILNR cam LQTCCDKPLLK cam cam LQTCCDKPLLKK cam cam LSQTFPNADFAEITK LVQEVTDFAK QEPERNECFLQHK cam RHPDYSVSLLLR RPCFSALTVDETYVPK cam RPCFSALTVDETYVPKEFK cam SLHTLFGDKLCAIPNLR cam TNCDLYEKLGEYGFQNAILVR cam TVMDDFAQFLDTCCK cam cam YMCENQATISSK ox cam YNDLGEQHFK YNDLGEQHFKGLVLIAFSQYLQK YTQKAPQVSTPTLVEAAR gi|42542817 Alpha fetoprotein ALQTMKQELLINLVK AQDQEVCFTEEGPK cam AQDQEVCFTEEGPKLISK cam CSQSGNLPGCQDNLEEELQK cam cam CSQSGNLPGCQDNLEEELQKHIEESQALSK cam cam DETYAPPPFSEDK EGSMLNEHVCSVIR cam ELREGSMLNEHVCSVIR ox cam FIYEVSRR LQNLFLIGYTR NPFMYAPAILSLAAQYDK ox NSGDGCLESQLSVFLDEICHETELSNK cam cam QKPELTEEQLAAVTADFSGLLEK QSCALYQTLGDYKLQNLFLIGYTR cam TAPASVPPFQFPEPAESCK cam TAPASVPPFQFPEPAESCKAHEENR cam THPNLPVSVILR VMTYICSQQNILSSK cam YGLSGCCSQSGVER cam cam gi|191765 Alpha fetoprotein APQVSTPTLVEAAR CCSGSLVER cam cam CCTLPEDQRLPCVEDYLSAILNR cam cam cam DVFLGTFLYEYSR HPDYSVSLLLR LGEYGFQNAILVR LPCVEDYLSAILNR cam LQTCCDKPLLK cam cam LQTCCDKPLLKK cam cam LSQTFPNADFAEITK LSQTFPNADFAEITKLATDLTK NYAEAKDVFLGTFLYEYSR RHPDYSVSLLLR TNCDLYEKLGEYGFQNAILVR cam VCLLHEKTPVSEHVTK cam YMCENQATISSK ox cam YTQKAPQVSTPTLVEAAR gi|191844 Alpha-1 protease AVLTIDETGTEAAAATVFEAVPMSMPPILR inhibitor 2 DQSPASHEIATNLGDFAISLYR FDHPFLFIIFEEHTQSPIFVGK FLEEAKNHYQAEVFSVNFAESEEAK IFNNGADLSGITEENAPLK IFNNGADLSGITEENAPLKLSK IVEAVKELDQDTVFALANYILFK KPFDPENTEEAEFHVDK KVINDFVEK LSISGDYNLK LSISGDYNLKTLMSPLGITR MQHLEQTLNK MQHLEQTLNKELISK NHYQAEVFSVNFAESEEAK NHYQAEVFSVNFAESEEAKK SFQHLLQTLNRPDSELQLSTGNGLFVNNDLK TLMSPLGITR VINDFVEKGTQGK WKKPFDPENTEEAEFHVDK gi|31982171 Alpha-2 ADSHFRHGIPFFVK macroglobulin MUG1 AHFSVMGDILSSAIR ALMAYAFALAGNQNK ALMAYAFALAGNQNKR ox ALSCLESSWK cam DGSYSAFGDQNGER EGNTWLTAFVLK ESGEKEEHSFTVMEFVLPR ESVVFVQTDKPVYKPGQSVK FALEIPVEFSMVPMAK ox ox FSTSQSLPASQTR HTNLVPHGTEKDVYR HTSSWLVTPK HVAYAVYSLSK LPIICFDYGMVPISAPR cam ox LQVTASPQSLCGLR cam LSEDQEDCILYSSWLAEK cam LSSSDEEDFLYVDIKGPTHEFSK LVDIKGDPIPNEK MLRPLNELLPLAYIEDPKK MLSGFIPLKPTVK MSLVLPPTVVK MSLVLPPTVVKDSAR NKESVVFVQTDKPVYKPGQSVK NLFDELVLDKDLFQCVSFIIPR cam QMSFSLAAEPIQGPYK ox QQNSNGGFSSTQDTVVALDALSK SLDEEAIKENNSIHWK SQKTTLVTIQSTGSFSQK TTLVTIQSTGSFSQK YTYGKPVPGHVK gi|7304875 Alpha-2-HS- ANLMHNLGGEEVSVACK cam glycoprotein (Fetuin) AQNVPLPVSTLVEFVIAATDCTAK cam CNLLAEK CNLLAEKQHGFCK cam cam ELACDDPEAEQVALLAVDYLNNHLLQGFK cam EVTDPAKCNLLAEK cam HAFSPVASVESASGETLHSPK QLTEHAVEGDCDFHILK cam QLTEHAVEGDCDFHILKQDGQFR cam QVLNQIDK QVLNQIDKVK TYHDLR VGQPGAAGPVSPMCPGR cam gi|14318646 Amylase 1, salivary AHFSISNSAEDPFIAIHAESKI AILDKLHNLNTK ALVFVDNHDNQR DFPGVPYSGFDFNDGK GHGAGGASILTFWDAR LSGLLDLALEKDYVR NWGEGWGLMPSDR ox SGNEDEFRDMVNR TAIVHLFEWR TASGGIENYQDAAQVR VADYMNHLIDIGVAGFR ox VMSSYYWPR WVDIAKECER cam gi|425520 Anti-colorectal ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK carcinoma light chain cam ASQDINSYLSWFQQKPGK HNSYTCEATHK cam MTQSPSSMYASLGER ox RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam TPAQFLGILLLWFPGMK ox gi|26345182 Apolipoprotein A1 ARPALEDLR (Unnamed protein DFANVYVDAVKDSGR product) DFWDNLEKETDWVR HSLMPMLETLK ox LAELKSNPTLNEYHTR LSPVAEEFRDR MRTHVDSLR QKLQELQGR QKVQPYLDEFQK SNPTLNEYHTR TQLAPHSEQMR TQLAPHSEQMRESLAQR ox TQVQSVIDKASETLTAQ VAPLGAELQESARQK VKDFANVYVDAVK VQPYLDEFQK VQPYLDEFQKK WKEDVELYR gi|14789706 Apolipoprotein A4 ALVQQLEQFR ALVQQLEQFRQQLGPNSGEVESHLSFLEK ATIDQNLEDLRR EAVEQFQKTDVTQQLSTLFQDK EKVNSFMSTLEK FLKAAVLTLALVAITGTR GSPDQPQALPLPEQAQEQAQEQAQEQVQPKPLES LGDASTYADGVHNK LNHQMEGLAFQMK LNHQMEGLAFQMKK LQEHLKPYAVDLQDQINTQTQEMK LQLTPYIQR LVPFVVQLSGHLAQETER MMPHANKVTQTFGENMQK ox NLAPLVEDVQSK NMEELKGHLTPR QLEQQVEEFRR QQLGPNSGEVESHLSFLEK SLAPLTVGVQEK SLAPLTVGVQEKLNHQMEGLAFQMK TDVTQQLSTLFQDK TDVTQQLSTLFQDKLGDASTYADGVHNK TVEPMGEMFNK VKGNTEGLQK VNSFMSTLEK gi|6753096 Apolipoprotein A-I AQSVIDKASETLTAQ ARPALEDLR DFANVYVDAVK DFWDNLEKETDWVR HSLMPMLETLK ox ox LAELKSNPTLNEYHTR LQELQGR LSPVAEEFR LSPVAEEFRDR MRTHVDSLR ox QEMNKDLEEVK ox QKLQELQGR THVDSLR TQLAPHSEQMR TQLAPHSEQMRESLAQR ox VAPLGAELQESARQK VKDFANVYVDAVK VQPYLDEFQK VQPYLDEFQKK WKEDVELYR gi|6753102 Apolipoprotein E AQAFGDRIR EHMEEVRSK ELEEQLGPVAEETR ELEEQLGPVAEETRAR ERLGPLVEQGR GRLEEVGNQAR GWFEPIVEDMHR ox LGADMEDLRNR LGKEVQAAQAR LGPLVEQGRQR LGQYRNEVHTMLGQSTEEIR LKGWFEPIVEDMHR LQAEIFQAR MEEQTQQIR NEVHTMLGQSTEEIRAR ox QWANLMEK SKMEEQTQQIR TANLGAGAAQPLRDR gi|1938223 Apolipoprotein H ATFGCHETYKLDGPEEAECTK cam cam (beta-2 glycoprotein) I ATVLYQGMR ox CLPHFAMIGNDTVMCTEQGNWTR ox cam cam CPFPPRPENGYVNYPAKPVLLYK cam CPFPPRPENGYVNYPAKPVLLYKDK cam CSYTVEAHCR cam cam DGTIEIPSCFKEHSSLAFWK cam FTCPLTGMWPINTLR cam ITCPPPPVPK cam KATVLYQGMR KCSYTVEAHCR cam cam RFTCPLTGMWPINTLR cam TGTWSFLPTCR cam TSYDPGEQIVYSCKPGYVSR cam VCPFAGILENGIVR cam WSPDIPACAR cam gi|9055162 Apolipoprotein M CVEEFQSLTSCLDFK cam cam CVEEFQSLTSCLDFKAFLVTPR cam cam FLLYNRSPHPPEK LTEGKGNMELR QLQLRATIR SPHPPEKCVEEFQSLTSCLDFK cam cam TDLFSSSCPGGIMLK cam ox TDLFSSSCPGGIMLKETGQGYQR cam TEGRPDMKTDLFSSSCPGGIMLK ox cam gi|2921308 Carboxylesterase DAGVSTYMYEFR precursor FAPPQPAEPWSFVK MNEETASLLLR MNEETASLLLR ox MNEETASLLLRR ox MVMKFWANFAR ox ox RFHSELNISESMIPAVIEK ox SELILDMFGDIFFGIPAVLMSR ox ox SFNTVPYIVGFNK SLRDAGVSTYMYEFR VLGKYISLEGFEQPVAVFLGVPFAKPPLGSLR YISLEGFEQPVAVFLGVPFAKPPLGSLR YRPSFVSDK gi|49523333 Clusterin ASGIIDTLFQDR (Apolipoprotein J) ASGIIDTLFQDRFFAR ELHDPHYFSPIGFPHK ELHDPHYFSPIGFPHKRPHFLYPK HTCMKFYAR cam ox QQSQVLDAMQDSFAR ox RPHFLYPK SLLNSLEEAKK TLIEKTNAER YINKEIQNAVQGVK gi|6753798 Coagulation factor II DNLSPPLGQCLTER cam (prothrombin) DTTEKELLDSYIDGR EECSVPVCGQEGR cam cam ENLDRDIALLK ETFMDCLEGR cam ETFMDCLEGR ox cam GIAPWQVMLFR GIAPWQVMLFRK ox GKYGFYTHVFR IRITDNMFCAGFK cam ITDNMFCAGFK cam KPVPFSDYIHPVCLPDKQTVTSLLR cam LYQGNLAVTTLGSPCLPWNSLPAK cam NPDSSTTGPWCYTTDPTVR cam REECSVPVCGQEGR cam cam RGDACEGDSGGPFVMK cam SGGSKDNLSPPLGQCLTER cam SPQELLCGASLISDR cam TFGLGEADCGLRPLFEK cam TLSKYQDFDPEVK TTDAEFHTFFNEK WYQMGIVSWGEGCDRK cam YNWRENLDR YTVCDSVRKPR cam gi|13624321 Coagulation factor CNEYYLLK cam XIII, beta subunit CNEYYLLKGSETSR cam CTAEGWSPNPR cam DAYISETSIAGSVLR DIVAYTCTAGYYTTTGK cam GDVRYPMCIR cam GMCASPPVIR cam IAQYYYTFK ILHGDLIDFVCK cam LIENGYFHPVK LSFFCLAGYATESGKQEEQIR cam QCDFPTVENGR cam QGYNLSPSIPLSEISAQCNR cam QTGEAECQANGWSLTPQCNK cam cam RDAYISETSIAGSVLR SFYFPMSVDK SFYFPMSVDKK ox TTGGKDEEVVHCLSAGWSSQPSCR cam cam VKDIVAYTCTAGYYTTTGK cam gi|6996919 Complememnt AEGIPEFYDYDVALVK histocompatibility 2, ALLDIGRDPK complement ALRLPQTATCK cam component factor B CLTNLIEKVASYGVRPR cam CPRPQDFENGEFWPR cam DVKALFVSEQGK FIQVGVISWGVVDVCR cam GDSGGPLIVHKR GGSFQLLQGGQALEYLCPSGFYPYPVQTR cam GNDYHKQPWQAK HVIIIMTDGLHNMGGNPVTVIQDIR ox KDNEHHVFK LEDIVTYHCSR cam LKYGQTLRPICLPCTEGTTR cam cam LNQISYEDHKLK NPREDYLDVYVFGVGPLVDSVNINALASK QHKEQLLPVK QQLVPSYAR RDLEIEEVLFHPK RQQLVPSYAR SLSLCGMVWEHK cam SLSLCGMVWEHKK cam SRFIQVGVISWGVVDVCR cam STGSWSDLQTR VKDASEVVTPR VKDMEDLENVFYQMIDETK ox ox VSDERSSDADWVTEK WDGQTAICDDGAGYCPNPGIPIGTR cam cam YGLLTYATVPK YGQTLRPICLPCTEGTTR cam cam gi|28175786 Complement C3 AAVFNHFISDGVKK precursor (HSE-MSF) AFYEHAPK AVMVSFQSGYLFIQTDK ox C47H50N3O7S2 (H+-Ion) DNHLAPGQQTTLR DNHLAPGQQTTLRIEGNQGAR DSCIGTLVVKGDPR cam EPGQDLVVLSLPITPEFIPSFR EVVADSVWVDVKDSCIGTLVVK cam FFKPAMPFDLMVFVTNPDGSPASK ox ox GDPRDNHLAPGQQTTLR IEGNQGAR IFTVDNNLLPVGK IRAFYEHAPK IRYYTYLVMNK ox ISLAHSLTR KVLMEGVRPSNADALVGK LESEETIVLEAHDAQGDIPVTVTVQDFLKR LSINTPNSR LVAYYTLIGASGQR MELKPGDNLNVNFHLR ox NVDGTAFVIFGVQDGDKK NYAGVFMDAGLAFK QIFSAEFEVK QPLTITVR QVLTSEKTVLTGASGHLR SGIPIVTSPYQIHFTK SLYVSVTVILHSGSDMVEAER ox TIYTPGSTVLYR TMEAHPYSTMHNSNNYLHLSVSR ox ox TSQGLQTEQR TVLTGASGHLR TVVILIETPDGIPVKR VEPTETFYYIDDPNGLEVSIIAK VGLVAVDKGVFVLNK VLMEGVRPSNADALVGK VVIEDGVGDAVLTR VVIEDGVGDAVLTRK YVTVVANFGETVVEK YYTYLVMNK gi|220349 Complement C4 APHIQLVAQSPWLR ATETQGVNLLFSSR ATETQGVNLLFSSRR FALMDEQGKR FVSSAFSLDLSR GHIFVQTDQPIYNPGQR GLETQAKLVEGR GTGFLSIEPLDPR HLVPGAHFLLQALVQEMSGSEASNVPVK ox KYVLPNFEVK LLLFSPSVVNLGTPLSVGVQLLDAPPGQEVK LLVSAGSLYPAIAR LSSGDDFVLLSLEVPLEDVR LTVQAPPSRGTGFLSIEPLDPR MRPSTDFLTITVENSHGLR ox NTAFKATETQGVNLLFSSR RAPHIQLVAQSPWLR RGHIFVQTDQPIYNPGQR SCGLFDLRR cam TFLRGLETQAK YIYGKPVQGVAYTR YVLPNFEVK gi|309119 Complement C4b- ATYTHRDSVR binding protein GKGVAWSNPFPECVIVK cam precursor HSGTEDFYPYNHGISYTCDPGFR cam IICSQPNILHGVIVSGYK cam IICSQPNILHGVIVSGYKATYTHR cam ITLVTYECDKGYR cam MMVYCKPSGEWEISVSCAK ox cam cam TMQYVPNSHDVK ox TVPVWSSSPPTCEK cam WKGTAPQCK cam YECLPGYGR cam gi|15030019 Complement ALVHLPLEYNSAVYSR component 6 ATDLQLSDVFLK CLPDRTWSQGDVECQR cam cam ECNNPAPQR cam FDPCQCAPCPNNGRPR cam cam cam FFPIPIFHFSEK FLCDSGRCIPSK cam cam FLYMEIHKEDTCTK cam GEVLDNSFTGGICK cam LSGTECLCVCQSGTYGENCER cam cam cam cam NEDSLSVDER NEHSHYSSAFNK NEHSHYSSAFNKVIK NIPCAVTKR cam NKFLCDSGR cam NKNEDSLSVDER QELQNSGLTEEEAQNCVQYETK cam QRQVVVNDYYWK QVVVNDYYWK SQQAAALAWEK SVLRPSQFGGQPCTEPLVTFQPCVPSK cam cam TKFFPIPIFHFSEK TRECNNPAPQR cam TSCLKPVVQDVLTISPFQR cam TVVSQGDVECQR cam VYQIGESIELTCPR cam YGGSFLQGSEK gi|27462724 Complement CIPACGVPTEPFQVHQR cam cam component C1SA IFGGQPAKIENFPWQVFFNHPR ISDPLMYVGTMSVR ox ox LQVVFTSDFSNEER LRYHGDPISCAK cam NQQFGPYCGNGFPGPLTIR cam SPNSPIIEEFQFPYNK WVNDQLGIELPR YHGDPISCAK cam gi|19072788 Complement CDNGFSPPSGYSWDYLR cam component factor h CIEKIPCSQPPTIEHGSINLPR cam cam CLPVTELENGR cam CSPPYILNGIYTPHR cam CTAQGWEPEVPCVR cam cam CTAQGWEPEVPCVRK cam cam CTLKPCEFPQFK cam cam CTLKPCEFPQFKYGR cam cam CTPTGWIPVPR cam CVATDQLEKCR cam cam CVEILCTPPR cam cam GDAVCTGSGWSSQPFCEEKR cam cam HTEKIYSHSGEDIEFGCK cam IIHRSDDEIR IKTCSASDIHIDNGFLSESSSIYALNR cam IPCSQPPTIEHGSINLPR cam IVSGAAETDQEYYFGQVVR KPCGHPGDTPFGSFR cam KVEYSHGEWK LYYEESLRPNFPVSIGNK LYYEESLRPNFPVSIGNKYSYK NGKWVASNPSR SCDMPVFENSITKNTR cam ox SDDEIRYECNYGFYPVTGSTVSK cam SYRTGEQVTFR TCGDIPELEHGSAK cam TSCPPPPQIPNTQVIETTVK cam VGDLLEFSCHSGHR cam VGPDSVQCYHFGWSPGFPTCK cam cam YRVGDLLEFSCHSGHR cam gi|6671744 Complement ECELPNSVPACVPWSPYLFQPNDR cam cam component factor i ITCGGIYIGGCWILTAAHCVRPSR cam cam cam SPSASDLPQEELVDQK VANYFDWISYHVGR VANYFDWISYHVGRSLVSQHNV VIGGKPANVGDYPWQVAIKDGQR VIVHEKYNGATFQNDIALIEMK gi|9954973 Complement D Chain DFDSVPPWR D, N-Terminally DICEGQVNSLPGSINK cam Truncated C3dg EADVSLTAFVLIALQEAR Fragment FLNTAKDR GYTQQLAFK KGYTQQLAFK QKPDGVFQEDGPVIHQEMIGGFR RQEALELIK WLILEK WLNDER gi|6754132 Complement AKGNEQSFHVSLR histocompatibility 2, APWMEQEGPEYWER Q region locus 10 APWMEQEGPEYWERETQR AYLEAECVEWLLR cam FDSDAETPRMEPR FIIVGYVDDTQFVR FIIVGYVDDTQFVRFDSDAETPR GNEQSFHVSLR GYLQYAYDGR GYLQYAYDGRDYIALNEDLK KWEQAGAAEYYR TDPPKTHVTHHPGSEGDVTLR THVTHHPGSEGDVTLR TWTAADVAAIITR WASVVVPLGK WEQAGAAEYYR YFETSVSRPGLGEPR YLELGKETLLR gi|54173 Contraspin ALYQTEAFTADFQQPTEAK AVLDVAETGTEAAAATGVIGGIR AVLDVAETGTEAAAATGVIGGI RK AVLPAVCFNRPFLIVIYHTSAQSILFMAK cam ox DLQILAEFHEK DLQILAEFHEKTR EVFTEQADLSGITEAK EVFTEQADLSGITEAKK FSIASDYRLEEDVLPEMGIK GKTMEEILEGLK ox HFRDEELSCSVLELK cam ISFDPQDTFESEFYLDEKR KLISELDDGTLMVLVNYIYFK ox KLSVSQVVHK KTLFSSQIEELNLPK LISELDDGTLMVLVNYIYFK ox MQQVEASLQPETLR MQQVEASLQPETLRK NIVFSPLSISAALALVSLGAK NQDKNIVFSPLSISAALALVSLGAK TLFSSQIEELNLPK TRALYQTEAFTADFQQPTEAK gi|38614350 Cp protein AEDEHLGILGPPIHANVGDK AEDEHLGILGPPIHANVGDKVK AEVEDKVYVHLK AGLQAFFQVR ALYFEYTDGTFSK DCNKPSPEDNIQDR cam DIFTGLIGPMKICK cam DLYSGLIGPLIVCR cam DTANLFPHK EMGPTYADPVCLSK ox cam ETFTYEWTVPK EYTDGSFTNR EYTDGSFTNRK GQHPLSIQPMGVSFTAENEGTYYGPPGR ox IYHSHVDAPK IYHSHVDAPKDIASGLIGPLILCK cam IYTFHAHGVTYTK KALYFEYTDGTFSK KLISVDTEQSNFYLQNGPDR LISVDTEQSNFYLQNGPDR MAYREYTDGSFTNR ox MFGNLQGLTMHVK ox ox MFTTAPDQVDKEDEDFQESNK ox MYYSGVDPTKDIFTGLIGPMK NMATRPYSIHAHGVK NMATRPYSIHAHGVK ox QFEDFTVYLGER QKYTVNQCQR cam RAEDEHLGILGPPIHANVGDK RDTANLFPHK SGAGREDSACIPWAYYSTVDR cam SLTLLMNPDTK ox TESSTVVPTLPGEVR TIDKPAWLGFLGPVIK TYTWQIPER TYYVAAVEVEWDYSPSR VFFEQGATR VKDLYSGLIGPLIVCR cam VNKDNEEFLESNK YTVNQCQR cam gi|19388017 Cpn2 protein AAHSQCAYSNPEGTVLLACEESR cam cam ALGLDEGEPAGSWDLTVEGR CRWLNIQLSSR cam DLRTLNLAQNLLTQLPK GAFQSLTGLQMLK GQLVPNLKQEQLICPVNPGHLSFR cam HLEPDAFGGLPR LFQSLRDLR LVSLTLSHNAITDLPEHVFR LVSLTLSHNAITDLPEHVFRNLEQLVK QEQLICPVNPGHLSFR cam TLNLAQNLLTQLPK TLPGRLFQSLR VVFLNTQVR WLNIQLSSR gi|11055360 Epidermal growth ACGPDYYEVEEDGIR cam factor receptor ACGPDYYEVEEDGIRK cam isoform 2 AVNHVCNPLCSSEGCWGPEPR cam cam cam CNILEGEPR cam FSNNPILCNMDTIQWR cam GPDNCIQCAHYIDGPHCVK cam cam cam GRSPSDCCHNQCAAGCTGPR cam cam cam cam IICAQQCSHR cam cam IPLENLQIIR KLFGTPNQK LTQLGTFEDHFLSLQR MYNNCEVVLGNLEITYVQR ox cam NLCYANTINWK cam NLCYANTINWKK cam NLQEILIGAVR NYVVTDHGSCVR cam SLKEISDGDVIISGNR SPSDCCHNQCAAGCTGPR cam cam cam cam TIQEVAGYVLIALNTVER TPPLDPRELEILK YCTAISGDLHILPVAFKGDSFTR cam YSFGATCVKK cam gi|6679689 Esterase 1 AISESGVVINTNVGKK FAPPQPAEPWSFVK ILSDMFSTEKEILPLK ox ISEDCLYLNIYSPADLTK cam KSELILDMFGDIFFGIPAVLLSR LKAEEVAFWTELLAK MNEETASLLLR MNEETASLLLRR MVMKFWANFAR NGNPNGEGLPHWPEYDEQEGYLQIGATTQQAQR QKTESELLEISGK RPQTVEGDHGDEIFFVFGAPLLK SELILDMFGDIFFGIPAVLLSR ox SFNTVPYIVGFNK SLRDAGVSTYMYEFR YISLEGFEQPVAVFLGVPFAKPPLGSLR YRPSFVSDK YRPSFVSDKRPQTVEGDHGDEIFFVFGAPLLK gi|33563252 Fibrinogen, alpha ALTEMRQMR ox ox polypeptide AQQIQALQSNVR AVNREINLQDYEGHQK DSDWPFCSDDDWNHKCPSGCR cam cam cam EINLQDYEGHQK EINLQDYEGHQKQLQQVIAK GDFANANNFDNTYGQVSEDLR GDFANANNFDNTYGQVSEDLRR GDFATRGPGSK GDSRGDFATR GLIDEANQDFTNR GLIDEANQDFTNRINK HPDLSGFFDNHFGLISPNFKEFGSK LKNSLFDFQR MADEAGSEAHREGETR MKGLIDEANQDFTNR MSPVPDLVPGSFK ox MSPVPDLVPGSFKSQLQEAPPEWK ox NNKDSNSLTR QYLPALKMSPVPDLVPGSFK ox RLEVDIDIK SQLQEAPPEWK SQLQEAPPEWKALTEMR THSDSDILTNIEDPSSHVPEFSSSSK VIEKAQQIQALQSNVR VTSSGTSTTHR gi|33859809 Fibrinogen, B beta AHYGGFTVQNEASK polypeptide AHYGGFTVQNEASKYQVSVNK EDGGGWWYNR EEPPSLRPAPPPISGGGYR ENENVINEYSSILEDQR GFGNIATNEDAK GFGNIATNEDAKK GGETSEMYLIQPDTSIKPYR GSWYSMRR ox HGTDDGWWMNWK IQKLESDISAQMEYCR cam IRPFFPQQ KEEPPSLRPAPPPISGGGYR KGGETSEMYLIQPDTSIKPYR LYIDETVNDNIPLNLR LYIDETVNDNIPLNLRVLR MGPTELLIEMEDWKGDK MSMKIRPFFPQQ ox QAQVKENENVINEYSSILEDQR QCSKEDGGGWWYNR cam QDGSVDFGRK SILEDLRSK TENGGWTVIQNR TPCTVSCNIPVVSGK cam cam TPCTVSCNIPVVSGKECEEIIR cam cam cam VYCDMKTENGGWTVIQNR cam YCGLPGEYWLGNDK cam YCGLPGEYWLGNDKISQLTR cam YYWGGLYSWDMSK gi|19527078 Fibrinogen, gamma AIQVYYNPDQPPKPGMIDSATQK polypeptide CHAGHLNGVYHQGGTYSK cam DNCCILDER cam cam EGFGHLSPTGTTEFWLGNEK ESGLYFIRPLK ESGLYFIRPLKAK FGSFCPTTCGIADFLSSYQTDVDNDLR cam cam GAKESGLYFIRPLK IHLISMQSTIPYALR IIPFNRLSIGEGQQHHMGGSK IQLKDWNGR LSIGEGQQHHMGGSK LSIGEGQQHHMGGSKQAGDV MVEEIVKYEALLLTHETSIR QQFLVYCEIDGSGNGWTVLQK cam QQFLVYCEIDGSGNGWTVLQKR cam RIDGSLDFK SSTTNGFDDGIIWATWK SSTTNGFDDGIIWATWKSR TSTADYAMFR WYSMKETTMK YLQEIYNSNNQK gi|1181242 Fibronectin ATGVFTTLQPLR DGQERDAPIVNR DTLTSRPAQGVITTLENVSPPRR FLTTTPNSLLVSWQAPR FTNIGPDTMR GGQPKQYNVGPLASK GVTYNIIVEALQNQR GVTYNIIVEALQNQRR NLQPGSEYTATLVAVK HHAEHSVGRPR IAGYRLTAGLTR IHLYTLNDNAR ITGYIIKYEKPGSPPR ITYGETGGNSPVQEFTVPGSK LGVRPSQGGEAPR LTCQCLGFGSGHFR cam cam NTFAEITGLSPGVTYLFK QYNVGPLASKYPLR SSPVIIDASTAIDAPSNLR STTPDITGYR TKTETITGFQVDAIPANGQTPVQR VTDATETTITISWR VTWAPPPSIELTNLLVR WLPSTSPVTGYR TVLVTWTPPR gi|46849812 Fibronectin 1 APITGYIIR ATGVFTTLQPLR CDPIDQCQDSETR cam cam CHEGGQSYK cam DGQERDAPIVNR DQCIVDDITYNVNDTFHK cam EYLGAICSCTCFGGQR cam cam cam FLTTTPNSLLVSWQAPR FTNIGPDTMR GDSPASSKPVSINYK GEWACIPYSQLR cam GGNSNGALCHFPFLYNNR cam GGQPKQYNVGPLASK GLTPGVIYEGQLISIQQYGHR GNLLQCVCTGNGR cam cam GRISCTIANR cam GVTYNIIVEALQNQR GVTYNIIVEALQNQRR HALQSASAGSGSFTDVR HHAEHSVGRPR HYQINQQWER IAGYRLTAGLTR IGDQWDKQHDLGHMMR ox IGDTWSK IGEKWDR IHLYTLNDNAR ISCTIANR cam ITGYIIKYEKPGSPPR ITYGETGGNSPVQEFTVPGSK LGVRPSQGGEAPR LTCQCLGFGSGHFR cam cam MSCTCLGNGKGEFK cam cam NLQPGSEYTVTLVAVKGNQQSPK NRCNDQDTR cam NTFAEITGLSPGVTYLFK QDRVPPSR QYNVGPLASKYPLR RPGAAEPSPDGTTGHTYNQYTQR SDNVPPPTDLQFVELTDVK SSPVIIDASTAIDAPSNLR STATINNIKPGADYTITLYAVTGR STTPDITGYR TEIDKPSQMQVTDVQDNSISVR ox TFYQIGDSWEK TFYSCTTEGR cam TKTETITGFQVDAIPANGQTPVQR VEVLPVSLPGEHGQR VFAVHQGR VTDATETTITISWR VTWAPPPSIELTNLLVR WCHDNGVNYK cam WKCDPIDQCQDSETR cam cam WKEATIPGHLNSYTIK WLPSTSPVTGYR WSRPQAPITGYR YEKPGSPPR YIVNVYQISEEGK YSFCTDHAVLVQTR cam YTGNTYK gi|28916693 Gelsolin AGKEPGLQIWR AVQHREVQGFESSTFSGYFK DGGQTAPASIR DPDQTDGPGLGYLSSHIANVER EPAHLMSLFGGKPMIIYK EVQGFESSTFSGYFK FDLVPVPPNLYGDFFTGDAYVILK GGVASGFKHVVPNEVVVQR HVVPNEVVVQR IEGSNKVPVDPATYGQFYGGDSYIILYNYR MDAHPPRLFACSNR ox cam NWRDPDQTDGPGLGYLSSHIANVER QTQVSVLPEGGETPLFKQFFK SEDCFILDHGR cam SEDCFILDHGRDGK cam SGALNSNDAFVLK SQHVQVEEGSEPDAFWEALGGK TASDFISKMQYPR ox TPSAAYLWVGAGASEAEK TPSAAYLWVGAGASEAEKTGAQELLK VEKFDLVPVPPNLYGDFFTGDAYVILK VPFDAATLHTSTAMAAQHGMDDDGTGQK VPVDPATYGQFYGGDSYIILYNYR VSEARPSTMVVEHPEFLK VSNGAGSMSVSLVADENPFAQGALR VVQGKEPAHLMSLFGGKPMIIYK ox YIETDPANR YIETDPANRDR gi|52843238 Glutathione FLVGPDGIPVMR ox peroxidase 3 LFWEPMKIHDIR MDILSYMRR ox NSCPPTAELLGSPGR cam QEPGENSEILPSLK TTVSNVKMDILSYMR ox WNFEKFLVGPDGIPVMR ox YVRPGGGFVPNFQLFEK YVRPGGGFVPNFQLFEKGDVNGEK gi|17512357 Gpld1 protein AQYVLTSPEASSR GIVATFYSHPR GKYHDVSER GRNQVVVAAGR IYDNLYGRK LGTSLSSGYVR LSGALHVYSFSSD NDFHRNLTMFISR ox NLRLMLAGSSQK ox NLTMFISRDIR SLGKVYGYFLPNR SSWGARLSGALHVYSFSSD TQPALLSTFSGDRR VYGYFLPNR WYVPVRDLLR YHDVSERTHWTPFLNASIHYIR gi|1694789 GRS protein LAQDYLQCVLQIPQPGSGPSK cam QNGGWENGFVKK SGWMTFLEVTGKICEMLSLLK cam TLFTQVMEK VLQNVAFSVQKEVEK gi|37719755 GUGU alpha AMFHINKPR AMFHINKPRR AMNQWVSGPAYYVEYLIK DGYMLSLNR ox DQKDGYMLSLNR EHYQEDMGSLFYLTLDVLETDCHVLSR ox cam GSIQHLPELDDEKPEESK HVPLIQPVEK ISAFDRFGR KTHTTCPDCPSPIDLSNPSALEAATESLAK cam cam LVVLPFPGKEQR MFYESVYGQCK cam MISAFDRFGR SAECPGPEKENNPLVLPP cam SQASCSLQHSDSEPVGICQGSTVQSSLR cam cam THTTCPDCPSPIDLSNPSALEAATESLAK cam cam gi|23956086 Hemopexin DYFVSCPGR cam ELGSPPGISLETIDAAFSCPGSSR cam FNPVTGEVPPR FNPVTGEVPPRYPLDAR GATYAFTGSHYWR GECQSEGVLFFQGNR cam GECQSEGVLFFQGNRK cam GGNNLVSGYPK GPDSVFLIK LFQEEFPGIPYPPDAAVECHR cam LWWLDLK LYVSSGRR RLWWLDLK SGAQATWTEVSWPHEK SGAQATWTEVSWPHEKVDGALCLDK cam SLGPNTCSSNGSSLYFIHGPNLYCYSSIDKLNAAK cam cam SLPQPQKVNSILGCSQ cam VWVYPPEKK WFWDFATR WKNPITSVDAAFR WLERYYCFQGNK cam YYCFQGNK cam YYCFQGNKFLR cam gi|150082914 High molecular ATSQVVAGTKYVIEFIAR weight kininogen I AYFPCIGCVHAISTDSPDLEPVLK cam cam isoform DeltaD5 CQALDMTEMAR ox cam ENEFFIVTQTCK cam FPSLHGDCVALPNGDDGECR cam cam LISDFPEATSPK RENEFFIVTQTCK cam RPPGFSPFR SGNQYMLHR TDGSPTFYSFK VIEGTKTDGSPTFYSFK gi|40715898 HMW-kininogen-II AKMDGSATFYSFNYQIK ox variant ATSQVVAGTNYVIEFIAR CQALDKTIPIR cam EGNCSAQRGLAWQDCDFK cam cam ENKFFIVTQTCK cam FFIVTQTCK cam GDCVALPNGDGGECR cam cam KATSQVVAGTNYVIEFIAR MDGSATFYSFNYQIK ox QLPRNVLGAHGSQLAGR RPPGFSPFR RRPPGFSPFR gi|31615671 Ig (A Chain A, Crystal ASQSISNNLHWYQQK Structure Of Fab DIVLTQSPATLSVTPGDSVSLSCR cam Fragment Of DSTYSMSSTLTLTKDEYER Antibody Hyhel-26 HNSYTCEATHK cam Complexed With QNGVLNSWTDQDSK Lysozyme) YASQSISGIPSR gi|4930001 Ig (A Chain A, IAVAWYQQKPGQSPK Idiotope-Anti-Idiotope DSTYSMSSTLTLTKDEYER ox Fab-Fab Complex) FMSTSVGDRVSITCK cam HNSYTCEATHK cam LLIYWASTR QNGVLDSWTDQDSK VSITCKASQDVR cam gi|11514687 Ig (A Chain A, Lyme ASQDINKYIAWYQHKPGK Disease Antigen DSTYSMSSTLTLTKDEYER ox Ospa In Complex HNSYTCEATHK cam With Neutralizing HNSYTCEATHKTSTSPIVK cam Antibody Fab La-2) QNGVLNSWTDQDSK RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam YIAWYQHKPGK gi|42543442 Ig (A Chain A, S25-2- DIVMSQSPSSLAVSAGEK ox Kdo Monosaccharide DSTYSMSSTLTLTKDEYER ox Complex) HNSYTCEATHK cam LLIYWASTR NYLAWYQQKPGQSPK QNGVLNSWTDQDSK TSTSPIVKSFNR gi|7766934 Ig (A Chain A, ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK Structure Of An cam Activity Suppressing DIVLTQSPASLAVSLGQR Fab Fragment To DIVLTQSPASLAVSLGQRATISCR cam Cytochrome P450 HNSYTCEATHK cam Aromatase) HNSYTCEATHKTSTSPIVK cam LLIYLVSNLESGVPAR gi|27373551 Ig (antibody variable DFQPGYNTGLK domain) FTISKTSTTVDLK GLEYIGFINPRGTPYYASWAK GTPYYASWAK IWGPGTLVTVSS gi|1870378 Ig (Anti-DNA ASQSISDYLHWYQQK immunoglobulin light ASQSISDYLHWYQQKSHESPR chain IgG) DIVMTQSPATLSVTPGDR ox DIVMTQSPATLSVTPGDRVSLSCR ox cam LLIKYASQSISGIPSR YASQSISGIPSR gi|12002896 Ig (anti-human ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK apolipoprotein A cam monoclonal antibody HNSYTCEATHK cam mAb(a)23L kappa HNSYTCEATHKTSTSPIVK cam light chain) LLIHYTSTLQPGIPSR RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam TFGGGTKLEIK YIAWYQHKPGKGPR gi|349893 Ig (C Chain C, Fab DSTYSMSSTLTLTKDEYER (Igg2a,Kappa) DVVMTQTPLSLPVSLGDQASISCR cam Fragment (26-10) FSGSGSGTDFTLK Complex With FSGVPDRFSGSGSGTDFTLK Digoxin) HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam QNGVLNSWTDQDSK TSTSPIVKSFNR VSNRFSGVPDR gi|47059057 Ig (gamma-2b- APQVYILPPPAEQLSR immunoglobulin) CPAPNLEGGPSVFIFPPNIKDVLMISLTPK cam ox LEPSGPISTINPCPPCKECHK cam cam cam SEDTAMYYCAR cam TTPPSVYPLAPGCGDTTGSSVTLGCLVK cam cam VNNKDLPSPIER VVSALPIQHQDWMSGKEFK ox gi|1806128 Ig (immunoglobulin ALPSPIEKTISKPR constant heavy chain) APQVYVLPPPAEEMTKK ECPPCAAPDLLGGPSVFIFPPK cam cam GPVRAPQVYVLPPPAEEMTK GSLFACSVVHEGLHNHLTTK cam NTATVLDSDGSYFMYSK TEQNYKNTATVLDSDGSYFMYSK ox TTAPSVYPLAPVCGGTTGSSVTLGCLVK cam cam VPITQNPCPPLK cam VPITQNPCPPLKECPPCAAPDLLGGPSVFIFPPK cam cam cam WSALPIQHQDWMSGK VVSALPIQHQDWMSGKEFK gi|10121892 Ig (immunoglobulin ALIYSASYR IgM MP-18-3-117 ASQNVGTNVAWYQQKPGQSPK kappa light chain) FMSTSVGDRVSVTCK cam FMSTSVGDRVSVTCK ox cam HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam gi|196723 Ig (immunoglobulin DVQITQSPSYLAASPGETITINCR cam kappa-chain VK-1) DVQITQSPSYLAASPGETITINCRASK cam LLIYSGSTLQSGIPSR SISKYLAWYQEKPGK TNKLLIYSGSTLQSGIPSR YLAWYQEKPGK YLAWYQEKPGKTNK gi|18033701 Ig (immunoglobulin ANGTPITQGVDTSNPTK light chain constant EGNKFMASSFLHLTSDQWR region) FMASSFLHLTSDQWR SHNSFTCQVTHEGDTVEK cam STPTLTVFPPSSEELKENK gi|13399686 Ig (L Chain L, 64m-2 ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK Antibody Fab cam Complexed With DSTYSMSSTLTLTKDEYER D(5ht)(6-4)t) DVLMTQTPLSLPVSLGDQASISCR cam FSGSGSGTDFTLK FSGVPDRFSGSGSGTDFTLK HNSYTCEATHK cam QNGVLNSWTDQDSK RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam SSQSIVHSNGNTYLEWYLQKPGQSPK VSNRFSGVPDR gi|3212470 Ig (L Chain L, Anti ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK Taq Fab Tp7) cam DEYERHNSYTCEATHK cam DIQMTQSPAIMSASPGEK ox ox DSTYSMSSTLTLTKDEYER FSGSGSGTSYSLTISR HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam LLIYDSTNLASGVPVR RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam gi|5542523 Ig (L Chain L, ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK Bactericidal Antibody cam Against Neisseria DIVMTQTPLSLPVSLGDKASISCR cam Meningitidis) DIVMTQTPLSLPVSLGDKASISCR ox cam DSTYSMSSTLTLTKDEYER ox FSGSGSGTDFTLK FSGVPDRFSGSGSGTDFTLK HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam QNGVLNSWTDQDSK TFGGGTKLEIK VSNRFSGVPDR gi|16975338 Ig (L Chain L, Crystal ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK Structure Of cam Immunoglobulin Fab ASGNIHNYLAWYQQK Fragment Complexed DEYERHNSYTCEATHK cam With 17-Beta- DIQMTQSPASLSASVGETVTITCR ox cam Estradiol) DSTYSMSSTLTLTKDEYER DSTYSMSSTLTLTKDEYER ox FSGSGSGTQYSLK HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam QNGVLNSWTDQDSK SPQLLVYNAK gi|18655521 Ig (L Chain L, Crystal ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK Structure Of The Fab cam Fragment Of The ASQSVDYDGDSYMNWYQQKPGQPPK Mouse Anti- Human ASQSVDYDGDSYMNWYQQKPGQPPK ox Fas Antibody Hfe7a) DIVLTQSPASLAVSLGQR DSTYSMSSTLTLTKDEYER DSTYSMSSTLTLTKDEYER ox HNSYTCEATHK cam LLIYAASNLESGIPAR gi|1942810 Ig (L Chain L, Fab ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK Fragment Of A cam Neutralizing Antibody DVVMTQTPLTLSVTIGQPASISCK cam Directed Against An DVVMTQTPLTLSVTIGQPASISCK ox cam Epitope Of Gp41 FTGSGSGTDFTLK From Hiv-1) HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam LDSGVPDRFTGSGSGTDFTLK LIYLVSKLDSGVPDR QNGVLNSWTDQDSK SSQSLLDSDGKTYLNWLLQRPGQSPK TFGGGTKLEIK VEAEDLGVYYCWQGTHFPR cam gi|7546516 Ig (L Chain L, Fab ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK Fragment Of cam Neutralising DIVLTQSPASLAVSLGQR Monoclonal Antibody HNSYTCEATHK cam 4c4 Complexed With LLIYRASNLESGIPAR G-H Loop From RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK Fmdv) cam gi|17943084 Ig (L Chain L, DSTYSMSSTLTLTKDEYER Structural Basis For DSTYSMSSTLTLTKDEYER ox Disfavored EVVMTQSPLSLPVSLGDQASISCR cam Elimination Reaction EVVMTQSPLSLPVSLGDQASISCR ox cam In Catalytic Antibody FSGSGSGTDFTLK 1d4) FSGVPDRFSGSGSGTDFTLK HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam QNGVLNSWTDQDSK SSQSLVHSNGNTYLHWYLQKPGQSPK TSTSPIVKSFNR VSNRFSGVPDR gi|2624743 Ig (L Chain L, DEYERHNSYTCEATHK cam Structure Of A DIVMTQSPLTLSVTIGQPASISCKSSQSLLYSNGK ox Catalytic Antibody, cam Igg2a Fab Fragment) DSTYSMSSTLTLTKDEYER DSTYSMSSTLTLTKDEYER ox FTGSGSGTDFTLK HNSYTCEATHK cam LDSGVPDRFTGSGSGTDFTLK QNGVLNSWTDQDSK gi|32263981 Ig (mAb FSGSGSGTSYSLTISR immunoglobulin light FSGSGSGTSYSLTISRMEAEDAATYYCQQR ox cam chain variable region) MEAEDAATYYCQQR cam MEAEDAATYYCQQR ox cam QIVLTQSPAIMSASPGEK ox SSYPFTFGSGTK SSYPFTFGSGTKLEIK gi|18568342 Ig (monoclonal CDIQMTQTTSALSASLGDR cam antibody BBK-2 light CDIQMTQTTSALSASLGDR cam ox chain) DSTYSMSSTLTLTKDEYER ox HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam MRFSAQFLGLLLLCFQGTR ox cam NLEQEDVATYFCQQGYTLPYTFGGGTKLEIK cam QNGVLNSWTDQDSK gi|52382 Ig (mu(b) DGKLVESGFTTDPVTIENK immunoglobulin DLHVPIPAVAEMNPNVNVFVPPR ox heavy chain) EFVCTVTHR cam EQLNLRESATVTCLVK cam FISKPNEVHK GFSPADISVQWLQR GVASVCVEDWNNR cam GVASVCVEDWNNRK cam HPPAVYLLPPAR KEFVCTVTHR cam LICEATNFTPKPITVSWLK cam LVESGFTTDPVTIENK LVESGFTTDPVTIENKGSTPQTYK NKDLHVPIPAVAEMNPNVNVFVPPR NKDLHVPIPAVAEMNPNVNVFVPPR ox NLVAMGCLAR cam NLVAMGCLAR ox cam SILEGSDEYLVCK cam TGGKYLATSQVLLSPK YLATSQVLLSPK gi|7439167 Ig (PC4436 APQVYTIPPPKEQMAK monoclonal antibody APQVYTIPPPKEQMAK ox 13-1 heavy chain) CRVNSAAFPAPIEK cam DCGCKPCICTVPEVSSVFIFPPKPK cam cam cam cam DDSKSSVYLQMNR GRPKAPQVYTIPPPK SNWEAGNTFTCSVLHEGLHNHHTEK cam TTPPSVYPLAPGSAAQTNSMVTLGCLVK ox cam VNSAAFPAPIEK VNSAAFPAPIEKTISK gi|15824610 Ig (Pterin-mimicking DIVLTQSPASLAVSLGQR anti-idiotope kappa FSGSGSGTDFTLNIHPVEEEDAATYYCQHSR cam chain variable region) LLIYLASNLESGVPAR ELPYTFGGGTKLEIK DIVLTQSPASLAVSLGQRATISCR cam gi|780265 Ig gamma-1 chain C APQVYTIPPPKEQMAK ox region (15C5) CRVNSAAFPAPIEK cam (fragment) NTQPIMDTDGSYFVYSKLNVQK ox SNWEAGNTFTCSVLHEGLHNHHTEK cam SVSELPIMHQDWLNGK SVSELPIMHQDWLNGK ox VNSAAFPAPIEK VNSAAFPAPIEKTISK gi|1799551 Ig gamma-chain, AQTPQVYTIPPPR secrete-type AQTPQVYTIPPPREQMSK AQTPQVYTIPPPREQMSK ox DALMISLTPK ox EVHTAWTQPR GYFPEPVTVK GYFPEPVTVKWNYGALSSGVR NTPPILDSDGTYFLYSK VNNKALPAPIER WSALPIQHQDWMR WSALPIQHQDWMR ox WNYGALSSGVR gi|223428 Ig H-C allotype APQVYILPPPAEQLSR gamma2b APQVYILPPPAEQLSRK CPAPNLEGGPSVFIFPPNIK cam CPAPNLEGGPSVFIFPPNIKDVLMISLTPK cam CPAPNLEGGPSVFIFPPNIKDVLMISLTPK cam ox GLVRAPQVYILPPPAEQLSR HEGLKNYYLK ISWFVNNVEVHTAQTQTHR LEPSGPISTINPCPPCKECHK cam cam cam TDSFSCNVR cam TDSFSCNVRHEGLK cam TTPPSVYPLAPGCGDTTGSSVTLGCLVK cam cam VNNKDLPSPIER VTCVVVDVSEDDPDVR cam WSALPIQHQDWMSGK WSALPIQHQDWMSGK ox WSALPIQHQDWMSGKEFK WSALPIQHQDWMSGKEFK ox WEKTDSFSCNVR cam gi|224008 Ig J chain CYTTMVPLR cam CYTTMVPLR cam ox CYTTMVPLRYHGETK cam CYTTMVPLRYHGETK cam ox IIPSTEDPNEDIVER IIPSTEDPNEDIVERNIR MVQAALTPDSCYPD ox cam NFVYHLSDVCK cam NFVYHLSDVCKK cam gi|12832551 Ig K (unnamed ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK protein product) cam ASENIYSNLAWYQQK ASENIYSNLAWYQQKQGK HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam QGKSPQLLVYAATNLADGVPSR RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam SPQLLVYAATNLADGVPSR gi|896077 Ig kappa chain ASSSVSSSYLHWYQQK ENVLTQSPAIMSASPGEK ox ENVLTQSPAIMSASPGEKVTMTCR ox cam ENVLTQSPAIMSASPGEKVTMTCR ox ox cam LWIYSTSNLASGVPAR SGASPKLWIYSTSNLASGVPAR gi|896089 Ig kappa chain DIVMSQSPSSLAVSVGEK ox ESGVPDRFTGSGSGTDFTLTISSVK FTGSGSGTDFTLTISSVK LLIYWASTR NYLAWYQQKPGQSPK SSQSLLYSSNQK gi|896103 Ig kappa chain ASQDIGSSLNWLQQEPDGTIKR DIQMTQSPSSLSASLGER DIQMTQSPSSLSASLGER ox LIYATSSLDSGVPK LIYATSSLDSGVPKR gi|896107 Ig kappa chain ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam ASENIYSNLAWYQQK ASENIYSNLAWYQQKQGK HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam QGKSPQLLVYAATNLADGVPSR RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam SPQLLVYAATNLADGVPSR gi|7513693 Ig kappa chain ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK (Mab03-1) cam DEYERHNSYTCEATHK cam DIVMTQSPSSLAMSVGQK DIVMTQSPSSLAMSVGQK ox DIVMTQSPSSLAMSVGQK ox ox DSTYSMSSTLTLTKDEYER ox HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam LLVYFASTR NYLAWYQQKPGQSPK SSQSLLNSRNQK gi|110429 Ig kappa chain V ASQDINKYIAWYQHKPGK region (9.42 DIQMTQSPSSLSASLGGK DIQMTQSPSSLSASLGGK ox LLIHYTSTLQPGIPSR YIAWYQHKPGK YIAWYQHKPGKGPR gi|49258884 Ig kappa chain V ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK region (D444) cam ASQSIGTDIHWYQQR DILLTQSPAILSVSPGER HNSYTCEATHK cam LLIKYASESISGIPSR RADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam YASESISGIPSR gi|930226 Ig kappa chain V ASQDIKSYLSWYQQKPWK region (hybridoma DIKMTQSPSSMYASLGER ox NC19-E11) DIKMTQSPSSMYASLGER ox ox MTQSPSSMYASLGER ox MTQSPSSMYASLGER ox ox SYLSWYQQKPWK SYLSWYQQKPWKSPK TLIYYATSLADGVPSR gi|125796 Ig kappa chain V-III ASESVDNYGISFMNWFQQKPGQPPK region PC 2880/PC ASESVDNYGISFMNWFQQKPGQPPK ox 1229 DIVLTQSPASLAVSLGQR EVPWTFGGGTK EVPWTFGGGTKLEIK LLIYAASNQGSGVPAR gi|197064 Ig kappa chain V- ASQDISNYLNWYQQKPDGTVK region (V-Jk1) protein DIQMTQTTSSLSASLGDR ox DIQMTQTTSSLSASLGDRVTISCR cam DIQMTQTTSSLSASLGDRVTISCR ox cam FSGSGSGTDYSLTISNLEQEDIATYFCQQGNTLPR cam LLIYYTSRLHSGVPSR TFGGGTKLEIK gi|1613779 Ig kappa light chain ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam ANRLVDGVPSR DIKMTQSPSSMYASLGER DIKMTQSPSSMYASLGER ox DIKMTQSPSSMYASLGER ox ox HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam MTQSPSSMYASLGER MTQSPSSMYASLGER ox MTQSPSSMYASLGER ox ox gi|284924 Ig light chain V region ASENIYSYLAWYQQK (clone 185-c1) DIQMTQSPASLSASVGETVTITCR ox cam FSGSGSGTQFSLK QGKSPQLLVYNAK SPQLLVYNAK TLAEGVPSRFSGSGSGTQFSLK gi|494164 Igg2a Fab Fragment ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK (Fab 179) cam DIVMTQSPSSLTVTAGEK ox HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam NYLTWYQQKPGQPPK gi|229901 Igg2b, Kappa ADAAPTVSIFPPSSEQLTSGGASVVCFLNNFYPK cam ASQDISNYLNWYQQKPDGTVK DIQMTQTTSSLSASLGDR DIQMTQTTSSLSASLGDR ox DIQMTQTTSSLSASLGDRVTISCR cam DIQMTQTTSSLSASLGDRVTISCR ox cam DSTYSMSSTLTLTKDEYER ox HNSYTCEATHK cam HNSYTCEATHKTSTSPIVK cam LLIYYTSR QNGVLNSWTDQDSK TFGGGTKLEIK gi|62204734 Inter alpha-trypsin ADAVQEATFQVELPR inhibitor, heavy chain AHGGTNINNAVLLAVELLDR 4 AHGGTNINNAVLLAVELLDRSNQAELLPSK DIVWEPPVEPDNTKR FKPTLSQQQK GSEMVVAGKLQDQGPDVLLAK ox ILKDLSPQDQFNLIEFSGEANQWK IRAHGGTNINNAVLLAVELLDR ITFELIYQELLQR ITFELIYQELLQRR LFVDPSQGLEVTGK LPLAAQAHPFRPPVR LWALLTIQQQLEQR MLSLPSVAQYPADPHLVVTEK ox NTEYKWK QSLVQATEENLNKAVNYASR QTEKFEVSVNVAPGSK QYSAAVGRGESAGIVK RLGMYELLLK RLGMYELLLK ox SQSEQDTVLNGDFIVR SVSLIILLTDGDPTVGETNPTIIQNNVR TLFSVLPGLK TVKVQGVDYLATR VQGVDYLATR VVNRADAVQEATFQVELPR YIFHNFMER YIFHNFMER ox YKFQHHFK gi|16418335 Leucine-rich alpha-2- CAGPEAMKGQR cam glycoprotein CAGPEAMKGQR cam ox DMQDGFDISHNPWICDKNLADLCR ox cam cam ELHLSSNRLQALSPELLAPVPR LEDSLLAPQPFLR LHLEGNRLQR LQALSPELLAPVPR LQRLEDSLLAPQPFLR gi|21594125 Lifr protein (leukemia AEIQLSKNDYIISVVAR inhibitory factor GAEDSTYHVAVDKLNPYTAYTFR receptor) HLTTEATPSKGPDTWR IASMEIPNDDITVEQAVGLGNR ox INLLCQIEICK cam cam LSCETHDLKEIICSWNPGR cam cam NDYIISVVAR NTEYTLFESISGK SEPCLLDWR cam YNFYLYGCTNQGYQLLR cam gi|8569601 Major urinary protein AGEYSVTYDGFNTFTIPK 1 DGETFQLMGLYGR ox EEASSTGRNFNVEK EKIEDNGNFR ENIIDLSNANR FAQLCEEHGILR cam FAQLCEEHGILRENIIDLSNANR cam IEDNGNFRLFLEQIHVLEK INGEWHTIILASDKR LFLEQIHVLEK TDYDNFLMAHLINEK ox gi|6754654 Mannose binding AIEEKLANMEAEIR lectin (A) AIEEKLANMEAEIR ox AIQEVATGIAFLGITDEATEGQFMYVTGGR ox GEPGQGLRGLQGPPGK LANMEAEIR ox LFVTNHEKMPFSK ox LQLTNKLHAFSMGK ox SLCTELQGTVAIPR cam SLCTELQGTVAIPRNAEENK cam VKSLCTELQGTVAIPR cam gi|233018 Mannose binding AEFDTSEIDSEIAALR protein C AEFDTSEIDSEIAALRSELR ALCSEFQGSVATPR cam ALRNWVLFSLSEK DIAYLGITDVR DIAYLGITDVRVEGSFEDLTGNR NWVLFSLSEK VAKDIAYLGITDVR VEGSFEDLTGNR VEGSFEDLTGNRVR VKALCSEFQGSVATPR cam WNDVPCSDSFLAICEFSD cam cam YTNWNDGEPNNTGDGEDCVVILGNGK cam gi|2118830 MHC class I AKGNEQSFHVSLR histocompatibility APWMEQEGPEYWER antigen H-2 Q10 APWMEQEGPEYWER ox alpha chain APWMEQEGPEYWERETQR APWMEQEGPEYWERETQR ox AYLEAECVEWLLR cam FDSDAETPRMEPR FDSDAETPRMEPR ox FIIVGYVDDTQFVR FIIVGYVDDTQFVRFDSDAETPR GNEQSFHVSLR GYLQYAYDGR GYLQYAYDGRDYIALNEDLK KWEQAGAAEYYR TDPPKTHVTHHPGSEGDVTLR THVTHHPGSEGDVTLR TWTAADVAAIITR WASVVVPLGK WEQAGAAEYYR YFETSVSRPGLGEPR YLELGKETLLR gi|387437 MHC factor B AEGIPEFYDYDVALVK ALFVSEQGK ALLDIGRDPK ALRLPQTATCK cam CLTNLIEK cam DNEHHVFK FIQVGVISWGVVDVCR cam FLCTGGVDPYADPNTCK cam cam GDSGGPLIVHKR GNDYHKQPWQAK HVIIIMTDGLHNMGGNPVTVIQDIR ox HVIIIMTDGLHNMGGNPVTVIQDIR ox ox ISVTRPLK KAEGIPEFYDYDVALVK KDNEHHVFK LKDEDLGFL LKYGQTLRPICLPCTEGTTR cam cam LNQISYEDHKLK RCLTNLIEK cam RDLEIEEVLFHPK SLSLCGMVWEHK cam SLSLCGMVWEHK cam ox SLSLCGMVWEHKK cam SLSLCGMVWEHKK cam ox VASYGVRPR VKDASEVVTPR VKDMEDLENVFYQMIDETK ox ox VSVGGQRR YGLLTYATVPK YGQTLRPICLPCTEGTTR cam cam gi|55217 Murine valosin- EAVCIVLSDDTCSDEKIR cam cam containing protein ELQELVQYPVEHPDKFLK EVDIGIPDATGRLEILQIHTK GILLYGPPGTGK GVLFYGPPGCGK cam IVSQLLTLMDGLK IVSQLLTLMDGLKQR IVSQLLTLMDGLKQR ox KYEMFAQTLQQSR ox MTNGFSGADLTEICQR ox cam QAAPCVLFFDELDSIAK cam WALSQSNPSALR gi|6679182 Orosomucoid 1 AVTHVGMDESEIIFVDWK ox AVTHVGMDESEIIFVDWKK AVTHVGMDESEIIFVDWKK ox HGAFMLAFDLKDEK HGAFMLAFDLKDEK ox RPDITPELR RPDITPELREVFQK WFFMGAAFR WFFMGAAFR ox YEGGVETFAHLIVLR YEGGVETFAHLIVLRK gi|31982113 Plasminogen [Mus CEGETDFVCR cam cam musculus] CQSWAAMFPHR cam CQSWAAMFPHR cam ox CQSWAAMFPHRHSK cam CQSWAAMFPHRHSK cam ox CTTPPPPPSPTYQCLK cam cam FTGQHFCGGTLIAPEWVLTAAHCLEK cam cam FVDWIEREMR FVDWIEREMR ox GENYRGTVSVTVSGK GKTAVTAAGTPCQGWAAQEPHR cam HNRTPENFPCK cam HSIFTPQTNPR HSKTPENFPDAGLEMNYCR cam HSKTPENFPDAGLEMNYCR ox cam KCQSWAAMFPHR cam KCQSWAAMFPHR cam ox LILEPNNRDIALLK LKEAQLPVIENK LSRPATITDK LSRPATITDKVIPACLPSPNYMVADR cam LSRPATITDKVIPACLPSPNYMVADR cam ox MRDVILFEK MRDVILFEK ox NLEENYCR cam NLEENYCRNPDGETAPWCYTTDSQLR cam cam NPDGDKGPWCYTTDPSVR cam NPDGDVNGPWCYTTNPR cam NPDGDVNGPWCYTTNPRK cam NPDGEPRPWCFTTDPTK cam NPDGEPRPWCFTTDPTKR cam NPDNDEQGPWCYTTDPDKR cam NYCRNPDGDVNGPWCYTTNPR cam cam QLAAGGVSDCLAK cam QLAAGGVSDCLAKCEGETDFVCR cam cam cam RVYLSECK cam SFQYHSKEQQCVIMAENSK cam TAVTAAGTPCQGWAAQEPHR cam TGIGNGYRGTMSR ox TICYITGWGETQGTFGAGR cam TPENFPCKNLEENYCR cam cam TPENFPDAGLEMNYCR cam TPENFPDAGLEMNYCR ox cam VCNRVEYLNNR cam VILGAHEEYIR VILGAHEEYIRGSDVQEISVAK VIPACLPSPNYMVADR cam VIPACLPSPNYMVADR cam ox VSRFVDWIER WEYCDIPR cam WEYCNLKR cam WGATFPHVPNYSPSTHPNEGLEENYCR cam WSEQTPHRHNR YDYCNIPECEEECMYCSGEKYEGK cam cam cam ox cam gi|2144495 PLMS plasmin CEGETDFVCR cam cam CQSWAAMFPHR cam CQSWAAMFPHR cam ox CTTPPPPPSPTYQCLK cam cam EQQCVIMAENSK cam ox FTGQHFCGGTLIAPEWVLTAAHCLEK cam cam FVDWIEREMR ox GENYRGTVSVTVSGK GKTAVTAAGTPCQGWAAQEPHR cam HSIFTPQTNPR KCQSWAAMFPHR cam KCQSWAAMFPHR cam ox LI LEPNNRDIALLK LKEAQLPVIENK LSRPATITDK LYDYCDIPLCASASSFECGKPQVEPKK cam cam cam MRDVILFEK MRDVILFEK ox NLEENYCR cam NPDGDKGPWCYTTDPSVR cam NPDGDVNGPWCYTTNPR cam NPDGETAPWCYTTDSQLR cam NPDNDEQGPWCYTTDPDKR cam NYCRNPDGDVNGPWCYTTNPR cam cam QLAAGGVSDCLAKCEGETDFVCR cam cam cam TAVTAAGTPCQGWAAQEPHR cam TICYITGWGETQGTFGAGR cam TPENFPDAGLEMNYCR cam TPENFPDAGLEMNYCR ox cam VCNRVEYLNNR cam VILGAHEEYIR VILGAHEEYIRGLDVQEISVAK VIPACLPSPNYMVADR cam VIPACLPSPNYMVADR cam ox VSRFVDWIER WEYCDIPR cam WEYCNLKR cam WSEQTPHRHNR gi|6680608 Pregnancy zone AAPLSLCALTAVDQSVLLLKPEAK cam protein AESPVFVQTDKPIYKPGQIVKFR AINYLISGYQR ALLAYAFALAGNK ALLAYAFALAGNKAK AMGVPMMGLDYSDEINQVVEVR ox ox EEGTGIELTGIGSCEIANALSKLK cam HSLGDNDAHSIFQSVGINIFTNSK HSLGDNDAHSIFQSVGINIFTNSKIHKPR LSPQSIYNLLPGK SKAINYLISGYQR SVIVEPEGIEK VKALSFYQPR VNTNYRPGLPFSGQVLLVDEK gi|53787 Properdin (AA 5 - CGGHCPGEAQQSQACDTQK cam cam cam 441) DIRVEDCCLNAAYAFQEHDGGLCQACR cam cam cam cam HCYNIHNCIMK cam cam HCYNIHNCIMK cam cam ox HGGPFCAGDATR cam HGGPFCAGDATRNQMCNK cam ox cam LQDIRHCYNIHNCIMK cam cam LQDIRHCYNIHNCIMK cam cam ox LRMSINCEGTPGQQSR cam LRMSINCEGTPGQQSR ox cam MSINCEGTPGQQSR cam MSINCEGTPGQQSR ox cam QRLCTPLLPK cam QRVCDNPAPK cam SCSAPAPSHQPPGKPCSGPAYEHK cam cam SRSCSAPAPSHQPPGKPCSGPAYEHK cam cam gi|49868 Put. beta-actin (aa DLYANTVLSGGTTMYPGIADR 27-375) DLYANTVLSGGTTMYPGIADR ox DSYVGDEAQSK DSYVGDEAQSKR GYSFTTTAER GYSFTTTAEREIVR HQGVMVGMGQK ox ox IWHHTFYNELR KDLYANTVLSGGTTMYPGIADR ox LCYVALDFEQEMATAASSSSLEK cam ox LDLAGRDLTDYLMK LDLAGRDLTDYLMK ox QEYDESGPSIVHR QEYDESGPSIVHRK SYELPDGQVITIGNER VAPEEHPVLLTEAPLNPK gi|34785996 Pzp protein AAPLSLCALTAVDQSVLLLKPEAK cam AESPVFVQTDKPIYKPGQIVK AESPVFVQTDKPIYKPGQIVKFR AFAQAQSHIFIEK AINYLISGYQR ALLAYAFALAGNK APSAEVEMTAYVLLAYLTSESSRPTR ox ATVLNYMSHCIQIR ox cam DAVKEEDSLHWQRPGDVQK DLTFYYLIK EEGTGIELTGIGSCEIANALSKLK cam ENGCFQQSGYLLNNAMK cam ENGCFQQSGYLLNNAMK cam ox GSGSGCVYLQTSLK cam GSIFNLGSHVLSLEQGNMK GSIFNLGSHVLSLEQGNMK ox HSLGDNDAHSIFQSVGINIFTNSK IHYLLNEDIMKNEK ox KIEHSFEVK KLQDQPNIQR LPDLPGNYVTK LSPQSIYNLLPGK LTEVPALVHKDTVVK NEKDLTFYYLIK SKAINYLISGYQR SQKEVLVTIESSGTFSK TEVNTNHVLIYIEK THITNAFNWLSMK ox TVQGAFFGVPVYK VKALSFYQPR VNTNYRPGLPFSGQVLLVDEK YNILPVADGK gi|33859612 Retinol binding DPNGLSPETR protein 4 DPNGLSPETRR FSGLWYAIAK FSGLWYAIAKK LLSNWEVCADMVGTFTDTEDPAKFK cam ox LQNLDGTCADSYSFVFSR cam LQNLDGTCADSYSFVFSRDPNGLSPETR cam MKYWGVASFLQR MKYWGVASFLQR ox QEELCLER cam QRQEELCLER cam QYRWIEHNGYCQSRPSR cam WIEHNGYCQSRPSR cam YWGVASFLQR gi|6678083 Serine (or cysteine) AVLTMDETGTEAAAATVLLAVPYSMPPIVR proteinase inhibitor, AVLTMDETGTEAAAATVLLAVPYSMPPIVR ox clade A, member 1 a AVLTMDETGTEAAAATVLLAVPYSMPPIVR ox ox DQSPASHEIATNLGDFAISLYR FDHPFLFIIFEEHTQSPLFVGK FLEEAKNHYQAEVFSVNFAESEEAK IFNNGADLSGITEENAPLK IFNNGADLSGITEENAPLKLSQAVHK KLDQDTVFALANYILFK KPFDPENTEEAEFHVDESTTVK LAQIHFPRLSISGEYNLK LDQDTVFALANYILFK LSISGEYNLK MQHLEQTLSKELISK NHYQAEVFSVNFAESEEAK NHYQAEVFSVNFAESEEAKK RLAQIHFPR SFQHLLQTLNRPDSELQLSTGNGLFVNNDLK SFQHLLQTLNRPDSELQLSTGNGLFVNNDLKLVEK TLMSPLGITR ox VINDFVEKGTQGK WKKPFDPENTEEAEFHVDESTTVK gi|15029662 Serine (or cysteine) DQSPASHEIATNLGDFAISLYR proteinase inhibitor, FDHPFLFIIFEEHTQSPIFVGK clade A, member 1 a IFNNGADLSGITEENAPLK IFNNGADLSGITEENAPLKLSQAVHK KLDQDTVFALANYILFK KPFDPENTEEAEFHVDESTTVK LDQDTVFALANYILFK LSISGEYNLK LSQAVHKAVLTIDETGTEAAAVTVLQMVPMSMPPILR ox ox ox MQHLEQTLSK NHYQAEVFSVNFAESEEAK NHYQAEVFSVNFAESEEAKK RLAQIHFPR TLMSPLGITR TLMSPLGITR ox VINDFVEKGTQGK WKKPFDPENTEEAEFHVDESTTVK gi|6678085 Serine (or cysteine) DQSPASHEIATNLGDFALR proteinase inhibitor, ELISQFLLNRR clade A, member 1d FDHPFLFIIFEEHTQSPIFVGK FLEEAKNHYQAEVFSVNFAESEEAK IFNNGADLSGITEENAPLK IFNNGADLSGITEENAPLKLSK KLDQDTVFALANYILFK KVINDFVEK LDQDTVFALANYILFK LSISGNYNLK MQHLEQTLNKELISQFLLNR NHYQAEVFSVNFAESEEAK NHYQAEVFSVNFAESEEAKK QPFDPENTEEAEFHVDESTTVK RSDAQIHIPR SDAQIHIPR TLMSPLGITR TLMSPLGITR ox TLMSPLGITRIFNNGADLSGITEENAPLK ox VINDFVEKGTQGK WKQPFDPENTEEAEFHVDESTTVK gi|6678087 Serine (or cysteine) DQSPASHEIATNLGDFAISLYR proteinase inhibitor, FLEEAKNHYQAEVFSVNFAESEEAK clade A, member 1e IFNSGADLSGITEENAPLK IFNSGADLSGITEENAPLKLSQAVHK KLEQDTVFVLANYILFK KPFDPENTK KVINDFVEK LAQIHIPRLSISGNYNLETLMSPLGITR LAQIHIPRLSISGNYNLETLMSPLGITR ox LEQDTVFVLANYILFK LSISGNYNLETLMSPLGITR LSISGNYNLETLMSPLGITR ox MQHLEQTLNKELISK MQHLEQTLNKELISK ox NHYQAEVFSVNFAESEEAKK QAEFHVDESTTVK RLAQIHIPR VINDFVEKGTQGK WKKPFDPENTK gi|18044689 Serine (or cysteine) ALYQTEAFTADFQQPTEAK proteinase inhibitor, AVLDVAETGTEAAAATGVIGGIR clade A, member 3K AVLDVAETGTEAAAATGVIGGIRK DLQILAEFHEK FSIASNYR HFRDEELSCSVLELK cam ISFDPQDTFESEFYLDEKR KTLFPSQIEELNLPK LALKNPDTNIVFSPLSISAALALVSLGAK MQQVEASLQPETLR ox MQQVEASLQPETLRK ox TLFPSQIEELNLPK TLMVLVNYIYFK ox gi|18252782 Serine (or cysteine) ANRPFLVLIR proteinase inhibitor, ANRPFLVLIREVALNTIIFMGR ox clade C ATEEDGSEQKVPEATNR (antithrombin), DIPVNPLCIYR cam member 1 DIPVNPLCIYRSPGK cam ENPEQSRVTINNWVANK EQLQDMGLIDLFSPEK ox EVALNTIIFMGR EVALNTIIFMGR ox FATNFYQHLADSK FRTEDGFSLK IKDVIPQGAINELTALVLVNTIYFK LQPLDFKENPEQSR NDNDNIFLSPLSISTAFAMTK ox QLMEVFKFDTISEK QLMEVFKFDTISEK ox SKFSPENTR SLNPNRVTFK SQLPGIVAGGRDDLYVSDAFHK SSDLVSANRLFGDK TSDQIHFFFAK VAEGTQVLELPFKGDDITMVLILPKPEK VAEGTQVLELPFKGDDITMVLILPKPEK ox VDGQSCPVPMMYQEGK cam ox ox VDGQSCPVPMMYQEGK ox cam gi|6679383 Serine (or cysteine) DFFHLDER proteinase inhibitor, FDPSLTQKDFFHLDER clade F, member 2 FTVSVDMMHAVSYPLR ox FTVSVDMMHAVSYPLR ox ox GFPIKDDFLEQSER LAPRMEEDYPQFSSPK ox LDNQDFGDHATLK LDNQDFGDHATLKR LFGAKPVK LIGQNDKADFHGGK LPLPALFK LTGKQEEDLANINQWVK NPNPSALPQLQEQR NPNPSALPQLQEQRDSPDNR QEEDLANINQWVK SVPTAEETRR WFLLEQPEIQVAHFPFK gi|15929675 Serpina 1a protein AVLTIDETGTEAAAVTVLLAVPYSMPPILR AVLTIDETGTEAAAVTVLLAVPYSMPPILR ox DQSPASHEIATNLGDFAISLYR FDHPFLFIIFEEHTQSPLFVGK FLEEAKNHYQAEVFSVNFAESEEAK IFNNGADLSGITEENAPLK IFNNGADLSGITEENAPLKLSQAVHK KLDQDTVFALANYILFK KPFDPENTEEAEFHVDESTTVK KVINDFVEK LDQDTVFALANYILFK LSISGEYNLK MQHLEQTLSK MQHLEQTLSK ox NHYQAEVFSVNFAESEEAK NHYQAEVFSVNFAESEEAKK RLAQIHFPR SFQHLLQTLNRPDSELQLSTGNGLFVNNDLK SFQHLLQTLNRPDSELQLSTGNGLFVNNDLKLVEK TLMSPLGITR TLMSPLGITR ox VINDFVEKGTQGK WKKPFDPENTEEAEFHVDESTTVK gi|14602605 Serpina1a protein AVLTIDETGTEAAAVTVLLAVPYSMPPILR AVLTIDETGTEAAAVTVLLAVPYSMPPILR ox DQSPASHEIATNLGDFAISLYR FDHPFLFIIFEEHTQSPLFVGK FLEEAKNHYQAEVFSVNFAESEEAK FLLNRR IFNNGADLSGITEENAPLK IFNNGADLSGITEENAPLKLSQAVHK KLDQDTVFALANYILFK KPFDPENTEEAEFHVDESTTVK KVINDFVEK LAQIHFPR LDQDTVFALANYILFK LSISGEYNLK MQHLEQTLSK ox NHYQAEVFSVNFAESEEAK NHYQAEVFSVNFAESEEAKK RLAQIHFPR SFQHLLQTLNRPDSELQLSTGNGLFVNNDLK TLMSPLGITR TLMSPLGITR ox TLMSPLGITRIFNNGADLSGITEENAPLK VINDFVEK VINDFVEKGTQGK WKKPFDPENTEEAEFHVDESTTVK gi|38174334 Serum amyloid P- APPSIVLGQEQDNYGGGFQR component EKVGEYSLYIGQSK EYTVKAPPSIVLGQEQDNYGGGFQR GRDNELLIYK SQSLFSYSVKGR TYSDLSRSQSLFSYSVK VFVFPRESETDHVK VGEYSLYIGQSK VGEYSLYIGQSKVTVR gi|20330802 Transferrin ADRDQYELLCLDNTR cam AVLTSQETLFGGSDCTGNFCLFK cam cam AVSSFFSGSCVPCADPVAFPK cam cam CAPNNKEEYNGYTGAFR cam CFVKLPEGTTPEK cam CLKDGGGDVAFVK cam CLVEKGDVAFVK cam DFASCHLAQAPNHVVVSR cam DFASCHLAQAPNHVVVSRK cam DFQLFSSPLGK DGGGDVAFVK DLLFKDSAFGLLR DLLFRDDTK DQYELLCLDNTR cam DSAFGLLR DSAFGLLRVPPR FDEFFSQGCAPGYEK cam GTDFQLNQLEGKK GYYAVAVVK HQTVLDNTEGKNPAEWAK IPSHAVVAR KPVKDFASCHLAQAPNHVVVSR cam KSCHTGLGR cam KSCHTGVDR cam LCQLCPGCGCSSTQPFFGYVGAFK cam cam cam cam LLEACTFHKH cam LYLGHNYVTAIR NLKQEDFELLCPDGTR cam NQQEGVCPEGSIDNSPVK cam NQQEGVCPEGSIDNSPVKVVCALSHLER cam cam SAGWVIPIGLLFCK cam SCHTGLGR cam SCHTGVDR cam SKDFQLFSSPLGK TAGWNIPMGMLYNR ox TAGWNIPMGMLYNR ox ox TSYPDCIK cam TVLPPDGPR VAQEHFGK VPPRMDYR ox WCALSHLER cam WCAVSEHENTK cam YLGAEYMQSVGNMR YLGAEYMQSVGNMR ox YLGAEYMQSVGNMRK YLGAEYMQSVGNMRK ox YLGAEYMQSVGNMRK ox ox gi|19354093 Transthyretin FVEGVYRVELDTK GSPAVDVAVKVFK HYTIAALLSPYSYSTTAVVSNPQN KTSEGSWEPFASGK LFLLCLAGLVFVSEAGPAGAGESKCPLMVK cam cam ox TAESGELHGLTTDEK TAESGELHGLTTDEKFVEGVYR TLGISPFHEFADVVFTANDSGHR TSEGSWEPFASGK VELDTKSYWK VLDAVRGSPAVDVAVK gi|111243 Vitamin D-binding CCESTSEDCMASELPEHTIK cam cam cam ox protein DLCGQSTTQAMDQYTFELSR cam DLCGQSTTQAMDQYTFELSR cam ox DLCGQSTTQAMDQYTFELSRR cam DLCGQSTTQAMDQYTFELSRR cam ox ECCDTQDSVACFSTQSPLLKR cam cam cam EWSLTEECCAEGADPTCYDTR cam cam cam FSSSTFEQVNQLVK GFADQFLYEYSSNYGQAPLPLLVAYTK GQEMCADYSENTFTEYK cam GQEMCADYSENTFTEYKK ox cam HLSLLTTMSNR HLSLLTTMSNR ox KFSSSTFEQVNQLVK KLCMAALSHQPQEFPTYVEPTNDEICEAFR cam ox cam LAQKVPTANLENVLPLAEDFTEILSR LPTGKDLCGQSTTQAMDQYTFELSR cam ox LQMKHLSLLTTMSNR ox NYLSMVGSCCTSANPTVCFVK cam cam cam NYLSMVGSCCTSANPTVCFVK ox cam cam cam QLTSFIEKGQEMCADYSENTFTEYK ox cam RTQVPEVFLSK SCESDAPFPVHPGTPECCTK cam cam cam SCESDAPFPVHPGTPECCTKEGLER cam cam cam SLSLILYSR TLRECCDTQDSVACFSTQSPLLK cam cam cam TQVPEVFLSK VCSQYAAYGK cam VCSQYAAYGKEK cam VPTANLENVLPLAEDFTEILSR gi|1083568 Zinc-alpha 2- AREEIFLVTLK glycoprotein AYLEEECPEMLKR cam AYLEEECPEMLKR cam ox CLAYGFYPQR cam FQATAFLNDQAFFHYNSNSGK GFSQSLSVQWDR SHLDRIDPPTVTITSR VIPGGNRIFK WEAEKVYVQR YAYDGEDFIEFNK Legenda \nox = methionin oxidation \ncam = carbamidomethyl oxidation References \n (1) Zerbini, A.; 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Dig Liver Dis. 2005, 37(4), 260-8 . The characteristics of the invention being disclosed in the preceding description, the subsequent drawings and claims can be of importance both singularly and in arbitrary combination for the implementation of the invention in its different embodiments. \nThe foregoing description of preferred embodiments of the invention has been presented for the purposes of illustration and description. It is not intended to be exhaustive or to limit the invention to the precise form described, and many modifications and variations are possible in light of the teaching above. The embodiments were chosen and described in order to best explain the principles of the invention and its practical applications to thereby enable others skilled in the art to best utilize the invention in various embodiments and with various modifications as are suited to the particular use contemplated invention being thus described, it will be obvious that the same may be varied in many ways. Such variations are not to be regarded as a departure from the spirit and scope of the invention, and all such modifications as would be obvious to one skilled in the art are intended to be included within the scope of the following claims.","lang":"en","source":"EPO_FULLTEXT","data_format":"ORIGINAL"}},"description_lang":["en"],"has_description":true,"has_docdb":true,"has_inpadoc":true,"has_full_text":true,"biblio_lang":"en"},"jurisdiction":"EP","collections":[],"usersTags":[],"lensId":"014-592-413-018-664","publicationKey":"EP_2071336_A1","displayKey":"EP 2071336 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Fib-g, ApoE, A2MG, A2MG isoform, Serpin, Clusterin, MHC-fB, SAP isoform, or from a second group consisting of Gpx3, properidin, MUP1, HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C, wherein the biomarker is regulated by EGF overexpression in a subject."],"number":1,"annotation":false,"claim":true,"title":false},{"lines":["Biomarker as claimed in claim 1 selected from a first group consisting of Amy 1, Apo Al, Carbx, Casp, Fib-a, Fib-b, Fib-g, Clusterin, MHC-fB, SAP isoform or from a second group consisting of HMW-K, Lifr-p, Orm 1, MBL-A, MBP-C."],"number":2,"annotation":false,"claim":true,"title":false},{"lines":["Biomarker as claimed in claim 1 selected from a first group consisting of AFP, ApoE, ApoM, or from a second group consisting of Gpx3, A2MG, A2MG isoform, SAP."],"number":3,"annotation":false,"claim":true,"title":false},{"lines":["A composition for qualifying the EGFR kinase activity in a subject suffering from or being susceptible to cancer, in particular by an in vitro body fluid analysis, comprising an effective amount of at least one biomarker selected from the first group according to one of the claims 1-3 or an effective amount of at least one biomarker selected from the second group according to one of the claims 1-3."],"number":4,"annotation":false,"claim":true,"title":false},{"lines":["Composition as claimed in claim 4 comprising an effective amount of at least one biomarker selected from the first group according to one of the claims 1-3 and an effective amount of at least one biomarker selected from the second group according to one of the claims 1-3."],"number":5,"annotation":false,"claim":true,"title":false},{"lines":["Use of a composition as claimed in one of the claims 4-5 for the production of a diagnostic agent, in particular of a diagnostic standard for body fluid analysis."],"number":6,"annotation":false,"claim":true,"title":false},{"lines":["Use as claimed in claim 6 for the production of a diagnostic agent for qualifying the EGFR kinase activity in a subject suffering from or being susceptible to cancer, in particular cancer of the liver, lung, breast, colon, prostate, bladder, head and neck, ovary or brain."],"number":7,"annotation":false,"claim":true,"title":false},{"lines":["Use as claimed in one of the claims 6-7 for the production of a diagnostic agent for predicting or monitoring the response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator."],"number":8,"annotation":false,"claim":true,"title":false},{"lines":["A kit for qualifying the EGFR kinase activity in a subject suffering from or being susceptible to cancer, in particular for predicting or monitoring the response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator, comprising at least one standard (1) indicative of the body fluid level of a biomarker selected from the first group according to one of the claims 1-3 in normal individuals or individuals having cancer associated with increased EGFR kinase activity and/or at least one standard (2) indicative of the body fluid level of a biomarker selected from the second group according to one of the claims 1-3 in normal individuals or individuals having cancer associated with increased EGFR kinase activity, and instructions for the use of the kit."],"number":9,"annotation":false,"claim":true,"title":false},{"lines":["The kit as claimed in claim 9, wherein the at least one standard (1) comprises an indicative amount of at least one biomarker selected from the first group according to one of the claims 1-3 and/or wherein the at least one standard (2) comprises an indicative amount of at least one biomarker selected from the second group according to one of the claims 1-3."],"number":10,"annotation":false,"claim":true,"title":false},{"lines":["The kit as claimed in one of the claims 9-10, comprising a mixture of the at least one standard (1) and the at least one standard (2), in particular the composition according to claim 5."],"number":11,"annotation":false,"claim":true,"title":false},{"lines":["The kit as claimed in one of the claims 9-11, further comprising a lysis buffer according to one of the claims 23-25 and/or a digesting buffer according to one of the claims 23-25."],"number":12,"annotation":false,"claim":true,"title":false},{"lines":["The kit as claimed in one of the claims 9-12, further comprising at least one antibody specific for a biomarker selected from the first group according to one of the claims 1-3 and/or at least one antibody specific for a biomarker selected from the second group according to one of the claims 1-3, and reagents effective to detect said biomarker(s) in a serum sample."],"number":13,"annotation":false,"claim":true,"title":false},{"lines":["The kit as claimed in claim 13, wherein the at least one antibody is polyclonal."],"number":14,"annotation":false,"claim":true,"title":false},{"lines":["The kit as claimed in one of the claims 13-14 comprising at least one labelled secondary antibody specific for the at least one antibody of claim 9-10."],"number":15,"annotation":false,"claim":true,"title":false},{"lines":["A method of qualifying the EGFR kinase activity in a subject, comprising determining in a body fluid sample of a subject suffering from or being susceptible to cancer at least one biomarker selected from the first group according to one of the claims 1-3 and/or at least one biomarker selected from the second group according to one of the claims 1-3, wherein the body fluid level of the at least one biomarker of said first group being significantly higher and/or the body fluid level of the at least one biomarker of said second group being significantly lower than the level of said biomarker(s) in the body fluid of subjects without cancer associated with increased activity of EGFR is indicative of induced EGFR kinase activity in the subject."],"number":16,"annotation":false,"claim":true,"title":false},{"lines":["Method as claimed in claim 16 for predicting the response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator, wherein the body fluid level of the at least one biomarker of said first group being significantly higher and/or the body fluid level of the at least one biomarker of said second group being significantly lower than the level of said biomarker(s) in the body fluid of subjects without cancer associated with increased activity of EGFR is indicative that the subject will respond therapeutically to a method of treating cancer comprising administering an EGFR kinase modulator."],"number":17,"annotation":false,"claim":true,"title":false},{"lines":["Method as claimed in claim 16 for monitoring the therapeutically response of a cancer patient to a method of treating cancer comprising administering an EGFR kinase modulator, wherein the body fluid level of the at least one biomarker of said first group before and after the treatment and/or the body fluid level of the at least one biomarker of said second group before and after the treatment is determined, and a significant decrease of said body fluid level(s) of the at least one biomarker of said first group and/or a significant increase of said body fluid level(s) of the at least one biomarker of said second group after the treatment is indicative that the cancer patient therapeutically responds to the administration of the EGFR kinase modulator."],"number":18,"annotation":false,"claim":true,"title":false},{"lines":["The method as claimed in one of the claims 16-18, wherein an immunoassay is performed, in particular by using the kit as claimed in one of the claims 9-15."],"number":19,"annotation":false,"claim":true,"title":false},{"lines":["The method as claimed in claim 19, wherein at least one antibody specific for a biomarker selected from the first group according to claim 2 and/or at least one antibody specific for a biomarker selected from the second group according to claim 2, and reagents effective to detect said biomarker(s) in a serum sample is used for the immunoassay."],"number":20,"annotation":false,"claim":true,"title":false},{"lines":["The method as claimed in one of the claims 16-18, wherein a peptide mass fingerprinting is performed, in particular by using the kit as claimed in one of the claims 9-12."],"number":21,"annotation":false,"claim":true,"title":false},{"lines":["The method as claimed in claim 21, comprising the steps of
- isolating a serum sample from a blood sample of a subject suffering from or being susceptible to cancer;
- adding lysis buffer to the serum sample;
- separating the proteins of the lysed serum sample by 2-DE gel electrophoresis;
- excising from the gel at least one sample containing a protein of interest;
- adding digesting buffer to the at least one excised sample;
- determining the amount of the at least one protein of interest by analyzing the at least one digest mixture by mass spectrometry."],"number":22,"annotation":false,"claim":true,"title":false},{"lines":["The method as claimed in claim 22, wherein
- the subject is a human patient or non-human transgenic animal; and/or
- the serum sample is isolated by centrifuging the blood sample; and/or
- the 2-DE is performed by using two different pH gradients; and/or
- the lysis buffer comprises (a) at least one buffer component, (b) at least one chaotrope, (c) at least one detergens, (d) at least one reducing agent (e) at least one carrier ampholyte, (f) at least one ribonuclease; and/or
- the protein of interest is a biomarker selected from the first group according to one of the claims 1-3 or a biomarker selected from the second group according to one of the claims 1-3; and/or
- the digesting buffer comprises a bicarbonate compound and a protease; and/or
- wherein the mass spectrometry is selected from the group consisting of MALDI-TOF and ESI-TOF."],"number":23,"annotation":false,"claim":true,"title":false},{"lines":["The method as claimed in one of the claims 22- 23, wherein
- the subject is suffering from or is susceptible to cancer in particular cancer of the liver, lung, breast, colon, prostate, bladder, head and neck, ovary or brain.; and/or
- the 2-DE is performed by using the pH gradients 3-10 and 4-7; and/or
- the lysis buffer is an aqueous solution of (a) at least one buffer compound selected from the group consisting of Tris and HEPES, (b) at least one chaotrope selected from the group consisting of urea and thiourea, (c) at least one detergens selected from the group consisting of CHAPS and SDS, (d) at least one reducing agent selected from the group consisting of DTT and TCEP, (e) at least one carrier ampholyte selected from the group consisting of biolyte 5-7 and biolyte 3-10, (f) at least one ribonuclease selected from the group consisting of endonuclease and exonuclease; and/or
- the protein of interest is a biomarker selected from the first group according to one of the claims 2-3 or a biomarker selected from the second group according to one of the claims 2-3; and/or
- the digesting buffer is an aqueous solution of at least one bicarbonate compound selected from the group consisting of ammonium bicarbonate and sodium bicarbonate and of at least one serine protease, in particular selected from the group consisting of trypsin, chymotrypsin and elastase; and/or
- the mass spectrometry is performed by MALDI-TOF; and/or
- a tandem mass spectrometer is used; and/or
- a matrix is used for the mass spectrometry selected from the group consisting of 3,5-dimethoxy-4-hydroxycinnamic acid, α-cyano-4-hydroxycinnamic acid and 2,5-dihydroxybenzoic acid."],"number":24,"annotation":false,"claim":true,"title":false},{"lines":["The method as claimed in one of the claims 22-24, wherein
- the subject is a transgenic mouse, in particular a mouse whose genome comprises a non natural IgEGF sequence; and/or
- the lysis buffer is an aqueous solution of (a) Tris; (b) urea and thiourea, (c) CHAPS, (d) DTT, (e) biolyte 3-10, (f) endonuclease; and/or
- the serum sample is calibrated or the serum samples are equilibrated to a predefined protein concentration by adding the lysis buffer; and/or
- the protein of interest is a biomarker selected from the first group according to claim 3 or a biomarker selected from the second group according to claim 3; and/or
- the digesting buffer is an aqueous solution of ammonium bicarbonate and trypsin; and/or
- a MALDI-TOF/TOF spectrometry is performed; and/or
- a matrix is used for the mass spectrometry selected from the group consisting of α-cyano-4-hydroxycinnamic acid."],"number":25,"annotation":false,"claim":true,"title":false},{"lines":["The method as claimed in one of the claims 22-25, further comprising the steps of
- determining the protein concentration of the serum sample, in particular by the Bradford method; and/or
- freezing and thawing the serum sample before the lysis buffer is added; and/or
- staining the gel after the 2-DE, in particular by using coomassie blue; and/or
- destaining the exised sample; and/or
- shrinking, in particular by adding acetonitrile, and drying of the excised sample before the digesting buffer is added; and/or
- using a peptide calibration standard for the mass spectrometry."],"number":26,"annotation":false,"claim":true,"title":false},{"lines":["A procedure to screen for and to identify drugs against cancer associated with an increased EGFR kinase activity comprising determining in a body fluid sample of a transgenic cancer mouse being treated with a compound to be tested, in particular of a mouse whose genome comprises a non natural IgEGF sequence, at least one biomarker selected from the first group according to one of the claims 1-3 and/or at least one biomarker selected from the second group according to one of the claims 1-3, wherein the body fluid level of the at least one biomarker of said first group being significantly lower and/or the body fluid level of the at least one biomarker of said second group being significantly higher than the level of said biomarker(s) in the body fluid of an untreated transgenic cancer mouse is indicative of the therapeutic effect of said compound as a EGFR kinase modulator."],"number":27,"annotation":false,"claim":true,"title":false},{"lines":["The procedure as claimed in claim 27, wherein the method as claimed in claim 18, in particular according to one of the claims 19-26, is used."],"number":28,"annotation":false,"claim":true,"title":false}]}},"filters":{"npl":[],"notNpl":[],"applicant":[],"notApplicant":[],"inventor":[],"notInventor":[],"owner":[],"notOwner":[],"tags":[],"dates":[],"types":[],"notTypes":[],"j":[],"notJ":[],"fj":[],"notFj":[],"classIpcr":[],"notClassIpcr":[],"classNat":[],"notClassNat":[],"classCpc":[],"notClassCpc":[],"so":[],"notSo":[],"sat":[]},"sequenceFilters":{"s":"SEQIDNO","d":"ASCENDING","p":0,"n":10,"sp":[],"si":[],"len":[],"t":[],"loc":[]}}