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本文引用的文献

1
Characterization of the heparin-binding site of the protein z-dependent protease inhibitor.鉴定蛋白 Z 依赖性蛋白酶抑制剂的肝素结合位点。
Biochemistry. 2012 May 15;51(19):4078-85. doi: 10.1021/bi300353c. Epub 2012 May 2.
2
Role of the residues of the 39-loop in determining the substrate and inhibitor specificity of factor IXa.39 环残基在决定因子 IXa 的底物和抑制剂特异性中的作用。
J Biol Chem. 2010 Sep 10;285(37):28488-95. doi: 10.1074/jbc.M110.143321. Epub 2010 Jul 13.
3
Molecular basis of factor IXa recognition by heparin-activated antithrombin revealed by a 1.7-A structure of the ternary complex.肝素激活的抗凝血酶识别因子 IXa 的分子基础通过三元复合物的 1.7A 结构揭示。
Proc Natl Acad Sci U S A. 2010 Jan 12;107(2):645-50. doi: 10.1073/pnas.0910144107. Epub 2009 Dec 22.
4
Structural basis of the cofactor- and substrate-assisted activation of human coagulation factor IXa.人凝血因子 IXa 的辅因子和底物辅助激活的结构基础。
Structure. 2009 Dec 9;17(12):1669-1678. doi: 10.1016/j.str.2009.10.011.
5
Crystal structure of protein Z-dependent inhibitor complex shows how protein Z functions as a cofactor in the membrane inhibition of factor X.蛋白Z依赖性抑制剂复合物的晶体结构揭示了蛋白Z如何作为辅助因子在膜上抑制因子X发挥作用。
Blood. 2009 Oct 22;114(17):3662-7. doi: 10.1182/blood-2009-04-210021. Epub 2009 Jun 15.
6
Kinetic characterization of the protein Z-dependent protease inhibitor reaction with blood coagulation factor Xa.蛋白Z依赖性蛋白酶抑制剂与凝血因子Xa反应的动力学特征
J Biol Chem. 2008 Oct 31;283(44):29770-83. doi: 10.1074/jbc.M805214200. Epub 2008 Sep 3.
7
Protein Z-dependent protease inhibitor binds to the C-terminal domain of protein Z.蛋白Z依赖性蛋白酶抑制剂与蛋白Z的C末端结构域结合。
J Biol Chem. 2008 Jul 18;283(29):19922-6. doi: 10.1074/jbc.M802639200. Epub 2008 May 23.
8
Serpins in thrombosis, hemostasis and fibrinolysis.丝氨酸蛋白酶抑制剂在血栓形成、止血和纤维蛋白溶解中的作用
J Thromb Haemost. 2007 Jul;5 Suppl 1(Suppl 1):102-15. doi: 10.1111/j.1538-7836.2007.02516.x.
9
FRET studies with factor X mutants provide insight into the topography of the membrane-bound factor X/Xa.对因子X突变体进行的荧光共振能量转移(FRET)研究有助于深入了解膜结合型因子X/Xa的拓扑结构。
Biochem J. 2007 Nov 1;407(3):427-33. doi: 10.1042/BJ20070735.
10
Expression, purification and characterization of factor IX derivatives using a novel vector system.使用新型载体系统对因子IX衍生物进行表达、纯化及特性鉴定
Protein Expr Purif. 2006 Dec;50(2):196-202. doi: 10.1016/j.pep.2006.05.012. Epub 2006 Jun 2.

39 环残基限制了因子 IXa 的血浆抑制剂特异性。

Residues of the 39-loop restrict the plasma inhibitor specificity of factor IXa.

机构信息

Edward A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University School of Medicine, St. Louis, Missouri 63104, USA.

出版信息

J Biol Chem. 2013 May 3;288(18):12692-8. doi: 10.1074/jbc.M113.459347. Epub 2013 Mar 25.

DOI:10.1074/jbc.M113.459347
PMID:23530052
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3642315/
Abstract

The two plasma inhibitors, protein Z-dependent protease inhibitor (ZPI) and tissue factor pathway inhibitor (TFPI), effectively inhibit the activity of activated factor X (FXa); however, neither inhibitor exhibits any reactivity with the homologous protease activated factor IX (FIXa). In this study, we investigated the molecular basis for the lack of reactivity of FIXa with these plasma inhibitors and discovered that unique structural features within residues of the 39-loop are responsible for restricting the inhibitor specificity of FIXa. This loop in FXa is highly acidic and contains three Glu residues at positions 36, 37, and 39. On the other hand, the loop is shorter by one residue in FIXa (residue 37 is missing), and it contains a Lys and an Asp at positions 36 and 39, respectively. We discovered that replacing residues of the 39-loop (residues 31-41) of FIXa with corresponding residues of FXa renders the FIXa chimera susceptible to inactivation by both ZPI and TFPI. Thus, the inactivation rate of the FIXa chimera by ZPI in the presence of protein Z (PZ), negatively charged membrane vesicles, and calcium ions approached the same diffusion-limited rate (>10(7) m(-1) s(-1)) that has been observed for the PZ-dependent inhibition of FXa by ZPI. Interestingly, sequence alignments indicated that, similar to FXa, residue 36 is a Glu in both mouse and bovine FIXa and that both proteases are also susceptible to inhibition by the PZ-ZPI complex. These results suggest that structural features within residues of the 39-loop contribute to the resistance of FIXa to inhibition by plasma inhibitors ZPI and TFPI.

摘要

两种血浆抑制剂,蛋白 Z 依赖性蛋白酶抑制剂(ZPI)和组织因子途径抑制剂(TFPI),能有效抑制激活的因子 X(FXa)的活性;然而,这两种抑制剂均与同源蛋白酶激活的因子 IX(FIXa)无反应性。在这项研究中,我们研究了 FIXa 与这些血浆抑制剂缺乏反应性的分子基础,并发现 39 环内独特的结构特征限制了 FIXa 对抑制剂的特异性。FXa 中的该环高度酸性,在位置 36、37 和 39 处含有三个谷氨酸残基。另一方面,FIXa 中的环短一个残基(缺失位置 37 的残基),并且在位置 36 和 39 处分别含有一个赖氨酸和天冬氨酸。我们发现,用 FXa 的相应残基替换 FIXa 的 39 环(残基 31-41)的残基,使 FIXa 嵌合体易受 ZPI 和 TFPI 的失活。因此,在蛋白 Z(PZ)、带负电荷的膜囊泡和钙离子存在下,ZPI 对 FIXa 嵌合体的失活速率接近观察到的 PZ 依赖性 ZPI 对 FXa 的抑制的相同扩散限制速率(>10(7) m(-1) s(-1))。有趣的是,序列比对表明,与 FXa 相似,36 位残基在鼠和牛 FIXa 中均为谷氨酸,并且这两种蛋白酶均易受 PZ-ZPI 复合物的抑制。这些结果表明,39 环内残基的结构特征有助于 FIXa 抵抗血浆抑制剂 ZPI 和 TFPI 的抑制。