| Literature DB >> 25046629 |
Volodymyr Chernyshenko1, Tetyana Platonova2, Yevgen Makogonenko2, Andriy Rebriev2, Lyuba Mikhalovska3, Tamara Chernyshenko2, Serhiy Komisarenko2.
Abstract
The variety of enzymes including serine proteases that possess fibrin(ogen)olytic and platelet modulating activity have been discovered in different snake venoms. In our work the fibrin(ogen)olytic and platelet modulating activity of a new protease from Echis multisquamatis snake venom was studied. It was shown that purified enzyme cleaved the ВβR42-A43 bond of fibrinogen during first contact with the substrate following much slower hydrolysis of C-terminus of fibrinogen Aα-chain. Protease hydrolysed fibrin clot too, but at much slower rate and cleaved both C-terminus of Aα-chain and ВβR42-A43 bond of Bβ-chain simultaneously. Preincubation of fibrinogen with protease dramatically elongated thrombin clotting time and the clot formed from a mixture of native fibrinogen and fibrinogen desВβ(1-42)2 digested by plasmin much faster than a native fibrin clot. The protease did not activate platelets nor cause changes in their shape and granularity, but it reduced platelets aggregation induced by ADP.Entities:
Keywords: Fibrin polymerization; Fibrinogen; Fibrinogenase; Platelet aggregation; Snake venom
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Year: 2014 PMID: 25046629 DOI: 10.1016/j.biochi.2014.06.015
Source DB: PubMed Journal: Biochimie ISSN: 0300-9084 Impact factor: 4.079