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Hemextin AB复合物——一种抑制因子VIIa活性的蛇毒抗凝血蛋白复合物。

Hemextin AB complex--a snake venom anticoagulant protein complex that inhibits factor VIIa activity.

作者信息

Banerjee Yajnavalka, Mizuguchi Jun, Iwanaga Sadaaki, Kini R Manjunatha

机构信息

Protein Science Laboratory, Department of Biological Sciences, Faculty of Science, National University of Singapore, Singapore.

出版信息

Pathophysiol Haemost Thromb. 2005;34(4-5):184-7. doi: 10.1159/000092420.

Abstract

Snake venom is a veritable gold mine of bioactive molecules, capable of binding to a wide variety of pharmacological targets, including the blood coagulation cascade. Here, we report the isolation and characterization of two synergistically acting anticoagulant three-finger proteins, hemextin A and hemextin B, from the venom of Hemachatus haemachatus (African Ringhals cobra). Hemextin A but not hemextin B exhibits mild anticoagulant activity. However, hemextin B interacts with hemextin A and forms a complex (hemextin AB complex), and synergistically enhances its anticoagulant potency. Prothrombin time assay showed that these two proteins form a 1:1 complex. Using a 'a dissection approach', we found that hemextins A and AB complex prolong clotting by inhibiting extrinsic tenase activity. Further studies showed that hemextin AB complex potently inhibits the proteolytic activity of factor VIIa (FVIIa) and its complexes. Kinetic studies showed that hemextin AB complex is a non-competitive inhibitor of FVIIa-soluble tissue factor proteolytic activity with a K(i) of 25 nM. Hemextin AB complex is the first reported natural inhibitor of FVIIa that does not require either tissue factor or factor Xa scaffold to mediate its inhibitory activity. Molecular interactions of hemextin AB complex with FVIIa/tissue factor-FVIIa may provide a new paradigm in the search for anticoagulants inhibiting the initiation of blood coagulation.

摘要

蛇毒是生物活性分子的真正宝库,能够与多种药理学靶点结合,包括血液凝固级联反应。在此,我们报告了从黑曼巴蛇(非洲环颈眼镜蛇)毒液中分离并鉴定出两种具有协同作用的抗凝三指蛋白——血纤蛋白A和血纤蛋白B。血纤蛋白A具有轻微的抗凝活性,而血纤蛋白B没有。然而,血纤蛋白B与血纤蛋白A相互作用并形成复合物(血纤蛋白AB复合物),并协同增强其抗凝效力。凝血酶原时间测定表明这两种蛋白形成1:1复合物。通过“剖析方法”,我们发现血纤蛋白A和血纤蛋白AB复合物通过抑制外源性凝血酶原激酶活性来延长凝血时间。进一步研究表明,血纤蛋白AB复合物能有效抑制因子VIIa(FVIIa)及其复合物的蛋白水解活性。动力学研究表明,血纤蛋白AB复合物是FVIIa-可溶性组织因子蛋白水解活性的非竞争性抑制剂,其抑制常数(K(i))为25 nM。血纤蛋白AB复合物是首个被报道的不需要组织因子或因子Xa支架来介导其抑制活性的FVIIa天然抑制剂。血纤蛋白AB复合物与FVIIa/组织因子-FVIIa的分子相互作用可能为寻找抑制血液凝固起始的抗凝剂提供新的范例。

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