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Studies of the heterogeneity of antithrombin III concentrates
Author(s) -
Barrowcliffe T. W.,
Eggleton C. Anne,
Mahmoud M.
Publication year - 1983
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/j.1365-2141.1983.tb01222.x
Subject(s) - antithrombin , heparin , chemistry , thrombin , immunoelectrophoresis , affinity chromatography , antigen , biochemistry , anticoagulant , binding site , chromatography , immunology , enzyme , biology , medicine , platelet
S ummary . The biological activities of antithrombin III (At III) concentrates, prepared by several manufacturers for clinical use, have been compared by three assay methods, and their heparin‐binding properties studied by crossed immunoelectrophoresis and heparin affinity chromatography. Concentrates from two of the four manufacturers showed discrepancies between assay methods, with concentrations by heparin co‐factor assays significantly lower than those by immunological and progressive antithrombin methods. Heterogeneity was also found by heparin binding studies, with about half the total At III antigen in these concentrates being unable to bind to heparin. These results confirm previous findings of heterogeneity in At III concentrates and show that some concentrates contain substantial amounts of altered At III molecules in which the heparin‐binding site has been denatured but the thrombin‐neutralizing site left largely intact.