An Antithrombin-Heparin Complex Increases the Anticoagulant Activity of Fibrin Clots
Lesley J. Smith, Tracy Anne Mewhort‐Buist, Leslie Roy Berry, Anthony K.C. Chan
Abstract
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Lesley J. Smith, Tracy Anne Mewhort‐Buist, Leslie Roy Berry, Anthony K.C. Chan
Abstract
Open-access reader
Clotting blood contains fibrin-bound thrombin, which is a major source of procoagulant activity leading to clot extension and further activation of coagulation. When bound to fibrin, thrombin is protected from inhibition by antithrombin (AT) + heparin but is neutralized when AT and heparin are covalently linked (ATH). Here, we report the surprising observation that, rather than yielding an inert complex, thrombin-ATH formation converts clots into anticoagulant surfaces that effectively catalyze inhibition of thrombin in the surrounding environment.
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Clotting blood contains fibrin-bound thrombin, which is a major source of procoagulant activity leading to clot extension and further activation of coagulation. When bound to fibrin, thrombin is protected from inhibition by antithrombin (AT) + heparin but is neutralized when AT and heparin are covalently linked (ATH). Here, we report the surprising observation that, rather than yielding an inert complex, thrombin-ATH formation converts clots into anticoagulant surfaces that effectively catalyze inhibition of thrombin in the surrounding environment.
Key concepts: Thrombin, Antithrombin, Fibrin, Heparin, Chemistry, Coagulation, Anticoagulant, Biochemistry