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全长和截短的重组组织因子途径抑制剂对人凝血因子Xa的抑制动力学

Kinetics of the inhibition of human factor Xa by full-length and truncated recombinant tissue factor pathway inhibitor.

作者信息

Lindhout T, Willems G, Blezer R, Hemker H C

机构信息

Department of Biochemistry, Cardiovascular Research Institute Maastricht, University of Limburg, The Netherlands.

出版信息

Biochem J. 1994 Jan 1;297 ( Pt 1)(Pt 1):131-6. doi: 10.1042/bj2970131.

Abstract

The inhibition equilibrium and kinetics of association and dissociation of the binding of three types of recombinant tissue factor pathway inhibitor (TFPI), namely full-length TFPI, C-terminal-truncated TFPI, and TFPI without the third Kunitz domain (TFPI1-161), to factor Xa have been measured. Formation and dissociation of the complexes were monitored by continuous measurement of the changes in the rate of hydrolysis of a peptidyl-p-nitroanilide substrate. Progress curves of product formation were fitted to a set of equations describing a one-step bimolecular inhibitory reaction in the presence of a competing substrate. For full-length TFPI the rate constants of association (kon) and dissociation (koff) were (5.1 +/- 0.7) x 10(6) M-1.s-1 and (2.6 +/- 0.9) x 10(-4)s-1 respectively. Thus, although the inhibition constant (50 pM) is far below the plasma concentration (2.5 nM) of TFPI, the half-time for transition to equilibrium in plasma is rather long (66s). The truncated forms of TFPI differ in that they have a 4-fold lower kon value but a similar dissociation rate constant. Therefore the inhibition constant, Ki, is 4-fold higher (0.2 nM) and the half-time to achieve equilibrium is prolonged to 250 s. The kon values of full-length and C-terminal-truncated TFPI, but not that of TFPI1-161, were found to decrease with increasing ionic strength.

摘要

已测定了三种类型的重组组织因子途径抑制剂(TFPI),即全长TFPI、C端截短的TFPI和不含第三个Kunitz结构域的TFPI(TFPI1-161)与因子Xa结合的抑制平衡以及结合和解离的动力学。通过连续测量肽基对硝基苯胺底物水解速率的变化来监测复合物的形成和解离。产物形成的进程曲线拟合为一组描述在存在竞争性底物时一步双分子抑制反应的方程。对于全长TFPI,结合速率常数(kon)和解离速率常数(koff)分别为(5.1±0.7)×10(6) M-1·s-1和(2.6±0.9)×10(-4)s-1。因此,尽管抑制常数(50 pM)远低于TFPI的血浆浓度(2.5 nM),但在血浆中达到平衡的半衰期相当长(66秒)。TFPI的截短形式的不同之处在于它们的kon值低4倍,但解离速率常数相似。因此,抑制常数Ki高4倍(0.2 nM),达到平衡的半衰期延长至250秒。发现全长和C端截短的TFPI的kon值会随着离子强度的增加而降低,但TFPI1-161的kon值不会。

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