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对结合到脂质纳米盘上的内源性凝血酶原酶复合物进行小角X射线散射分析,突出了凝血因子VIIIa/IXa之间的分子间接触。

SAXS analysis of the intrinsic tenase complex bound to a lipid nanodisc highlights intermolecular contacts between factors VIIIa/IXa.

作者信息

Childers Kenneth C, Peters Shaun C, Lollar Pete, Spencer Harold Trent, Doering Christopher B, Spiegel Paul C

机构信息

Department of Chemistry, Western Washington University, Bellingham, WA; and.

Department of Pediatrics, Aflac Cancer and Blood Disorders Center, Children's Healthcare of Atlanta, Emory University, Atlanta, GA.

出版信息

Blood Adv. 2022 Jun 14;6(11):3240-3254. doi: 10.1182/bloodadvances.2021005874.

Abstract

The intrinsic tenase (Xase) complex, formed by factors (f) VIIIa and fIXa, forms on activated platelet surfaces and catalyzes the activation of factor X to Xa, stimulating thrombin production in the blood coagulation cascade. The structural organization of the membrane-bound Xase complex remains largely unknown, hindering our understanding of the structural underpinnings that guide Xase complex assembly. Here, we aimed to characterize the Xase complex bound to a lipid nanodisc with biolayer interferometry (BLI), Michaelis-Menten kinetics, and small-angle X-ray scattering (SAXS). Using immobilized lipid nanodiscs, we measured binding rates and nanomolar affinities for fVIIIa, fIXa, and the Xase complex. Enzyme kinetic measurements demonstrated the assembly of an active enzyme complex in the presence of lipid nanodiscs. An ab initio molecular envelope of the nanodisc-bound Xase complex allowed us to computationally model fVIIIa and fIXa docked onto a flexible lipid membrane and identify protein-protein interactions. Our results highlight multiple points of contact between fVIIIa and fIXa, including a novel interaction with fIXa at the fVIIIa A1-A3 domain interface. Lastly, we identified hemophilia A/B-related mutations with varying severities at the fVIIIa/fIXa interface that may regulate Xase complex assembly. Together, our results support the use of SAXS as an emergent tool to investigate the membrane-bound Xase complex and illustrate how mutations at the fVIIIa/fIXa dimer interface may disrupt or stabilize the activated enzyme complex.

摘要

由因子(f)VIIIa和fIXa形成的内源性凝血酶原酶(Xase)复合物在活化的血小板表面形成,并催化因子X活化为Xa,刺激血液凝固级联反应中凝血酶的产生。膜结合Xase复合物的结构组织在很大程度上仍然未知,这阻碍了我们对指导Xase复合物组装的结构基础的理解。在这里,我们旨在通过生物层干涉术(BLI)、米氏动力学和小角X射线散射(SAXS)来表征与脂质纳米盘结合的Xase复合物。使用固定化脂质纳米盘,我们测量了fVIIIa、fIXa和Xase复合物的结合速率和纳摩尔亲和力。酶动力学测量表明在脂质纳米盘存在下活性酶复合物的组装。纳米盘结合的Xase复合物的从头算分子包络使我们能够通过计算模拟停靠在柔性脂质膜上的fVIIIa和fIXa,并确定蛋白质-蛋白质相互作用。我们的结果突出了fVIIIa和fIXa之间的多个接触点,包括在fVIIIa A1-A3结构域界面处与fIXa的新型相互作用。最后,我们在fVIIIa/fIXa界面鉴定了具有不同严重程度的血友病A/B相关突变,这些突变可能调节Xase复合物的组装。总之,我们的结果支持使用SAXS作为研究膜结合Xase复合物的新兴工具,并说明了fVIIIa/fIXa二聚体界面处的突变如何破坏或稳定活化的酶复合物。

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