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外切酶加速血液凝固。

Exosites expedite blood coagulation.

机构信息

Biochemistry Department, Universidade Federal de São Paulo, São Paulo-SP, Brazil.

Biodiscovery Institute, School of Pharmacy, University of Nottingham, Nottingham, United Kingdom.

出版信息

J Biol Chem. 2020 Nov 6;295(45):15208-15209. doi: 10.1074/jbc.H120.016301.

Abstract

A careful balance between active-site and exosite contributions is critically important for the specificity of many proteases, but this balance is not yet defined for some of the serine proteases that serve as coagulation factors. Basavaraj and Krishnaswamy have closed an important gap in our knowledge of coagulation factor X activation by the intrinsic Xase complex by showing that exosite binding plays a critical role in this process, which they describe as a "dock and lock." This finding not only significantly enhances our understanding of this step in the coagulation cascade and highlights parallels with the prothrombinase complex, but will also provide a novel rationale for inhibitor development in the future.

摘要

在许多蛋白酶中,活性位点和变构位点的贡献之间的精细平衡对于其特异性至关重要,但对于一些作为凝血因子的丝氨酸蛋白酶,这种平衡尚未确定。Basavaraj 和 Krishnaswamy 通过显示变构位点结合在该过程中起着关键作用,从而填补了我们对内源性 Xase 复合物激活凝血因子 X 知识的重要空白,他们将该过程描述为“对接和锁定”。这一发现不仅极大地提高了我们对凝血级联反应这一步骤的理解,并突出了与凝血酶原酶复合物的相似之处,而且还为未来的抑制剂开发提供了新的依据。

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本文引用的文献

1
Exosite binding drives substrate affinity for the activation of coagulation factor X by the intrinsic Xase complex.
J Biol Chem. 2020 Nov 6;295(45):15198-15207. doi: 10.1074/jbc.RA120.015325. Epub 2020 Aug 28.
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Recent Insights Into the Regulation of Coagulation and Thrombosis.
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