z-logo
Premium
Ca 2+ ‐induced binding of anticoagulation factor II from the venom of Agkistrodon acutus with factor IX
Author(s) -
Shen DengKe,
Xu XiaoLong,
Zhang Yan,
Song JiaJia,
Yan XinCheng,
Guo MingChun
Publication year - 2012
Publication title -
biopolymers
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.556
H-Index - 125
eISSN - 1097-0282
pISSN - 0006-3525
DOI - 10.1002/bip.22078
Subject(s) - chemistry , circular dichroism , in vivo , thrombin , venom , factor x , biophysics , factor ix , binding site , coagulation , partial thromboplastin time , thromboplastin , tissue factor , biochemistry , medicine , platelet , microbiology and biotechnology , biology
Anticoagulation factor II (ACF II), a coagulation factor X‐ binding protein from the venom of Agkistrodon acutus has both anticoagulant and hypotensive activities. Previous studies show that ACF II binds specifically with activated factor X (FXa) in a Ca 2+ ‐dependent manner and inhibits intrinsic coagulation pathway. In this study, the inhibition of extrinsic coagulation pathway by ACF II was measured in vivo by prothrombin time assay and the binding of ACF II to factor IX (FIX) was investigated by native polyacrylamide gel electrophoresis and surface plasmon resonance (SPR). The results indicate that ACF II also inhibits extrinsic coagulation pathway, but does not inhibit thrombin activity. ACF II also binds with FIX with high binding affinity in a Ca 2+ ‐dependent manner and their maximal binding occurs at about 0.1 m M Ca 2+ . ACF II has similar binding affinity to FIX and FX as determined by SPR. Ca 2+ has a slight effect on the secondary structure of FIX as determined by circular dichroism spectroscopy. Ca 2+ ions are required to maintain in vivo function of FIX Gla domain for its recognition of ACF II. However, Ca 2+ at high concentrations (>0.1 m M ) inhibits the binding of ACF II to FIX. Ca 2+ functions as a switch for the binding between ACF II and FIX. ACF II extends activated partial thromboplastin time more strongly than prothrombin time, suggesting that the binding of ACF II with FIX may play a dominant role in the anticoagulation of ACF II in vivo. © 2012 Wiley Periodicals, Inc. Biopolymers 97: 818–824, 2012.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here