Krishnaswamy S
Department of Medicine, Emory University School of Medicine, Atlanta, Georgia 30322.
J Biol Chem. 1992 Nov 25;267(33):23696-706.
The interaction of factor VIIa with tissue factor (TF) results in an increase in the catalytic efficiency for the hydrolysis of several synthetic peptidyl p-nitroanilide substrates by factor VIIa. The binding of human recombinant factor VIIa to recombinant human TF incorporated into vesicles containing phosphatidylcholine (TF/PC) or phosphatidylcholine/phosphatidylserine (TF/PCPS) was studied using the increased rate of H-D-phenylalanyl L-pipecoyl L-arginine p-nitroanilide (S2238) hydrolysis as a signal for the interaction. The saturable dependence of rate on increasing concentrations of factor VIIa or TF/PCPS yielded no obvious evidence for cooperativity and could be analyzed according to the interaction of factor VIIa with independent noninteracting sites (Kd = 259 +/- 60 pM, n = 1.05 +/- 0.12 mol of factor VIIa/mol of TF at saturation). Identical titration curves and equilibrium parameters were derived from titrations using TF/PC or TF in the absence of phospholipids, indicating that possible protein-membrane interactions do not further stabilize the extrinsic Xase complex. The dissociation constant for the interaction of factor VIIa with TF/PCPS inferred from measurements of factor X activation (Kd = 197 +/- 38 pM) was comparable with the values obtained from measurements of S2238 hydrolysis. In contrast to the membrane-independent nature of the enzyme-cofactor interaction, the rate of factor X activation was reduced by approximately 50-fold when the enzyme complex was assembled using solution-phase TF. Collectively, the result indicate that the membrane dependence of extrinsic Xase function primarily results from an influence of the membrane surface on factor X utilization.
因子VIIa与组织因子(TF)相互作用,使因子VIIa对几种合成肽基对硝基苯胺底物水解的催化效率提高。利用H-D-苯丙氨酰-L-哌啶甲酰-L-精氨酸对硝基苯胺(S2238)水解速率的增加作为相互作用的信号,研究了重组人因子VIIa与掺入含磷脂酰胆碱的囊泡(TF/PC)或磷脂酰胆碱/磷脂酰丝氨酸(TF/PCPS)中的重组人TF的结合。速率对因子VIIa或TF/PCPS浓度增加的饱和依赖性未显示出协同作用的明显证据,并且可以根据因子VIIa与独立的非相互作用位点的相互作用进行分析(Kd = 259 +/- 60 pM,饱和时n = 1.05 +/- 0.12摩尔因子VIIa/摩尔TF)。使用TF/PC或无磷脂情况下的TF进行滴定得到了相同的滴定曲线和平衡参数,表明可能的蛋白质-膜相互作用不会进一步稳定外源性X酶复合物。从因子X激活测量推断的因子VIIa与TF/PCPS相互作用的解离常数(Kd = 197 +/- 38 pM)与从S2238水解测量获得的值相当。与酶-辅因子相互作用的非膜依赖性性质相反,当使用溶液相TF组装酶复合物时,因子X激活速率降低了约50倍。总体而言,结果表明外源性X酶功能的膜依赖性主要源于膜表面对因子X利用的影响。