Fast functional protein C assay using protac® a novel protein C activator
A simple and rapid clotting method for the quantitative determination of protein C (PC) in plasma consists of the conversion of PC into activated PC (APC) by means of Protac®, an activator protein isolated from Agkistrodon contortrix contortrix venom, of the subsequent degradation of factors V and V...
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Veröffentlicht in: | Thrombosis research 1986-08, Vol.43 (3), p.253-264 |
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description | A simple and rapid clotting method for the quantitative determination of protein C (PC) in plasma consists of the conversion of PC into activated PC (APC) by means of Protac®, an activator protein isolated from Agkistrodon contortrix contortrix venom, of the subsequent degradation of factors V and VIII in PC immuno-depleted plasma by the generated APC and of the measurement of the prolongation of the activated partial thromboplastin time (APTT) which is proportional to the amount of PC in the sample. In 33 normal individuals a mean PC level of 97.1% of a normal pooled plasma was found. Comparison with an enzyme-immunoassay for PC in 33 patients with liver disease revealed a good correlation (r = 0.986). Patients under warfarin therapy (n = 34) had a mean PC level of 19.8%; a comparison with the immunological assay (mean value = 55.3%) in the same population suggested that the assay did not coestimate acarboxy forms of PC. The assay proved to be insensitive to heparin concentration lower than 1 U/ml. Due to its simplicity, it should be suitable for diagnostic routine and monitoring of patients with abnormal PC level, even if under anticoagulation. |
doi_str_mv | 10.1016/0049-3848(86)90145-3 |
format | Article |
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In 33 normal individuals a mean PC level of 97.1% of a normal pooled plasma was found. Comparison with an enzyme-immunoassay for PC in 33 patients with liver disease revealed a good correlation (r = 0.986). Patients under warfarin therapy (n = 34) had a mean PC level of 19.8%; a comparison with the immunological assay (mean value = 55.3%) in the same population suggested that the assay did not coestimate acarboxy forms of PC. The assay proved to be insensitive to heparin concentration lower than 1 U/ml. Due to its simplicity, it should be suitable for diagnostic routine and monitoring of patients with abnormal PC level, even if under anticoagulation.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/0049-3848(86)90145-3</identifier><identifier>PMID: 3526629</identifier><identifier>CODEN: THBRAA</identifier><language>eng</language><publisher>New York, NY: Elsevier Ltd</publisher><subject>Anticoagulants - therapeutic use ; Biological and medical sciences ; Blood Coagulation Tests ; Blood coagulation. Blood cells ; Crotalid Venoms ; Fundamental and applied biological sciences. Psychology ; General aspects, investigation methods, hemostasis, fibrinolysis ; Glycoproteins - blood ; human plasma ; Humans ; Immunoenzyme Techniques ; liver disease ; Liver Diseases - blood ; Molecular and cellular biology ; oral anticoagulation ; Partial Thromboplastin Time ; Peptides ; Protein C ; protein C assay</subject><ispartof>Thrombosis research, 1986-08, Vol.43 (3), p.253-264</ispartof><rights>1986</rights><rights>1987 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c386t-6f120f27df52d783ed9a4c792f2aae022a213ee3486529084a5a5a8d3555d1563</citedby><cites>FETCH-LOGICAL-c386t-6f120f27df52d783ed9a4c792f2aae022a213ee3486529084a5a5a8d3555d1563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0049-3848(86)90145-3$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27911,27912,45982</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=8039889$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3526629$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Martinoli, J.L.</creatorcontrib><creatorcontrib>Stocker, K.</creatorcontrib><title>Fast functional protein C assay using protac® a novel protein C activator</title><title>Thrombosis research</title><addtitle>Thromb Res</addtitle><description>A simple and rapid clotting method for the quantitative determination of protein C (PC) in plasma consists of the conversion of PC into activated PC (APC) by means of Protac®, an activator protein isolated from Agkistrodon contortrix contortrix venom, of the subsequent degradation of factors V and VIII in PC immuno-depleted plasma by the generated APC and of the measurement of the prolongation of the activated partial thromboplastin time (APTT) which is proportional to the amount of PC in the sample. In 33 normal individuals a mean PC level of 97.1% of a normal pooled plasma was found. Comparison with an enzyme-immunoassay for PC in 33 patients with liver disease revealed a good correlation (r = 0.986). Patients under warfarin therapy (n = 34) had a mean PC level of 19.8%; a comparison with the immunological assay (mean value = 55.3%) in the same population suggested that the assay did not coestimate acarboxy forms of PC. The assay proved to be insensitive to heparin concentration lower than 1 U/ml. Due to its simplicity, it should be suitable for diagnostic routine and monitoring of patients with abnormal PC level, even if under anticoagulation.</description><subject>Anticoagulants - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Blood Coagulation Tests</subject><subject>Blood coagulation. Blood cells</subject><subject>Crotalid Venoms</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects, investigation methods, hemostasis, fibrinolysis</subject><subject>Glycoproteins - blood</subject><subject>human plasma</subject><subject>Humans</subject><subject>Immunoenzyme Techniques</subject><subject>liver disease</subject><subject>Liver Diseases - blood</subject><subject>Molecular and cellular biology</subject><subject>oral anticoagulation</subject><subject>Partial Thromboplastin Time</subject><subject>Peptides</subject><subject>Protein C</subject><subject>protein C assay</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1986</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMlKxEAQhhtRxnF5A4UcRPQQ7T3dF0EGxwXBi56bslORlkyi3cmAL-VD-GRmFga8SB0Kqr6_KD5Cjhi9YJTpS0qlzYWR5szoc0uZVLnYImNmCptzWfBtMt4gu2QvpXdKWcGsGpGRUFxrbsfkYQqpy6q-8V1oG6izj9h2GJpskkFK8JX1KTRvyyn4n-8Msqad4x9sSM6ha-MB2amgTni47vvkZXrzPLnLH59u7yfXj7kXRne5rhinFS_KSvGyMAJLC9IXllccACnnwJlAFNJoxS01EtRQphRKqZIpLfbJ6eru8MNnj6lzs5A81jU02PbJFdoWWkk1gHIF-timFLFyHzHMIH45Rt1CoVv4cQs_zmi3VOjEEDte3-9fZ1huQmtnw_5kvYfkoa4iND6kDWaosMYssKsVhoOLecDokg_YeCxDRN-5sg3___ELjQaMiA</recordid><startdate>19860801</startdate><enddate>19860801</enddate><creator>Martinoli, J.L.</creator><creator>Stocker, K.</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19860801</creationdate><title>Fast functional protein C assay using protac® a novel protein C activator</title><author>Martinoli, J.L. ; Stocker, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c386t-6f120f27df52d783ed9a4c792f2aae022a213ee3486529084a5a5a8d3555d1563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1986</creationdate><topic>Anticoagulants - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Blood Coagulation Tests</topic><topic>Blood coagulation. Blood cells</topic><topic>Crotalid Venoms</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects, investigation methods, hemostasis, fibrinolysis</topic><topic>Glycoproteins - blood</topic><topic>human plasma</topic><topic>Humans</topic><topic>Immunoenzyme Techniques</topic><topic>liver disease</topic><topic>Liver Diseases - blood</topic><topic>Molecular and cellular biology</topic><topic>oral anticoagulation</topic><topic>Partial Thromboplastin Time</topic><topic>Peptides</topic><topic>Protein C</topic><topic>protein C assay</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Martinoli, J.L.</creatorcontrib><creatorcontrib>Stocker, K.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Martinoli, J.L.</au><au>Stocker, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fast functional protein C assay using protac® a novel protein C activator</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>1986-08-01</date><risdate>1986</risdate><volume>43</volume><issue>3</issue><spage>253</spage><epage>264</epage><pages>253-264</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><coden>THBRAA</coden><abstract>A simple and rapid clotting method for the quantitative determination of protein C (PC) in plasma consists of the conversion of PC into activated PC (APC) by means of Protac®, an activator protein isolated from Agkistrodon contortrix contortrix venom, of the subsequent degradation of factors V and VIII in PC immuno-depleted plasma by the generated APC and of the measurement of the prolongation of the activated partial thromboplastin time (APTT) which is proportional to the amount of PC in the sample. In 33 normal individuals a mean PC level of 97.1% of a normal pooled plasma was found. Comparison with an enzyme-immunoassay for PC in 33 patients with liver disease revealed a good correlation (r = 0.986). Patients under warfarin therapy (n = 34) had a mean PC level of 19.8%; a comparison with the immunological assay (mean value = 55.3%) in the same population suggested that the assay did not coestimate acarboxy forms of PC. The assay proved to be insensitive to heparin concentration lower than 1 U/ml. Due to its simplicity, it should be suitable for diagnostic routine and monitoring of patients with abnormal PC level, even if under anticoagulation.</abstract><cop>New York, NY</cop><pub>Elsevier Ltd</pub><pmid>3526629</pmid><doi>10.1016/0049-3848(86)90145-3</doi><tpages>12</tpages></addata></record> |
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subjects | Anticoagulants - therapeutic use Biological and medical sciences Blood Coagulation Tests Blood coagulation. Blood cells Crotalid Venoms Fundamental and applied biological sciences. Psychology General aspects, investigation methods, hemostasis, fibrinolysis Glycoproteins - blood human plasma Humans Immunoenzyme Techniques liver disease Liver Diseases - blood Molecular and cellular biology oral anticoagulation Partial Thromboplastin Time Peptides Protein C protein C assay |
title | Fast functional protein C assay using protac® a novel protein C activator |
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