Jordan R E, Oosta G M, Gardner W T, Rosenberg R D
J Biol Chem. 1980 Nov 10;255(21):10081-90.
The kinetics of inhibition of four hemostatic system enzymes by antithrombin were examined as a function of heparin concentration. Plots of the initial velocity of factor Xa-antithrombin or plasmin-antithrombin interaction versus the level of added mucopolysaccharide exhibit an ascending limb and subsequent plateau regions. In each case, the kinetic profile is closely correlated with the concentration of the heparin . antithrombin complex formed within the reaction mixture. A decrease in the velocity of inhibition is not observed at high levels of added mucopolysaccharide despite the generation of significant quantities of heparin-enzyme interaction products. The second-order rate constants for the neutralization of factor Xa or plasmin by the mucopolysaccharide . inhibitor complex are 2.4 x 10(8) M-1 min-1 and 4.0 x 10(6) M-1 min-1, respectively. These parameters must be contrasted with the similarly designated constants obtained in the absence of heparin which are 1.88 x 10(5) M-1 min-1 and 4.0 x 10(4) M-1 min-1, respectively. Plots of the initial velocity of the factor IXa-antithrombin or the thrombin-antithrombin interaction versus the level of added mucopolysaccharide exhibit an ascending limb, pseudoplateau, descending limb, and final plateau regions. In each case, the ascending limb and pseudoplateau are closely correlated with the concentration of heparin c antithrombin complex formed within the reaction mixture. Furthermore, the descending limb and final plateau of these two processes coincide with the generation of increasing amounts of the respective mucopolysaccharide-enzyme interaction products. The second-order rate constants for the neutralization of factor IXa or thrombin by the heparin . antithrombin complex are 3.0 x 10(8) M-1 min-1 and 1.7 x 10(9) M-1 min-1, respectively. The second-order rate constants for the inhibition of mucopolysaccharide-factor IXa or mucopolysaccharide-thrombin interaction products by the heparin . antithrombin complex are 2.0 x 10(7) M-1 min-1 and 3.0 x 10(8) M-1 min-1, respectively. These kinetic parameters must be contrasted with similarly designated constants obtained in the absence of mucopolysaccharide which are 2.94 x 10(4) M-1 min-1 and 4.25 x 10(5) M-1 min-1, respectively. Thus, our data demonstrate that binding of heparin to antithrombin is required for the mucopolysaccharide-dependent enhancement in the rates of neutralization of thrombin, factor IXa, factor Xa, or plasmin by the protease inhibitor. Furthermore, a careful comparison of the various constants suggests that the direct interaction between heparin and antithrombin may be largely responsible for the kinetic effect of this mucopolysaccharide.
研究了抗凝血酶对四种止血系统酶的抑制动力学与肝素浓度的关系。因子Xa-抗凝血酶或纤溶酶-抗凝血酶相互作用的初始速度与添加的粘多糖水平的关系图呈现一个上升段和随后的平台区。在每种情况下,动力学曲线都与反应混合物中形成的肝素-抗凝血酶复合物的浓度密切相关。尽管产生了大量的肝素-酶相互作用产物,但在高浓度添加粘多糖时未观察到抑制速度的降低。粘多糖-抑制剂复合物中和因子Xa或纤溶酶的二级速率常数分别为2.4×10⁸ M⁻¹ min⁻¹和4.0×10⁶ M⁻¹ min⁻¹。这些参数必须与在无肝素情况下获得的类似指定常数进行对比,后者分别为1.88×10⁵ M⁻¹ min⁻¹和4.0×10⁴ M⁻¹ min⁻¹。因子IXa-抗凝血酶或凝血酶-抗凝血酶相互作用的初始速度与添加的粘多糖水平的关系图呈现一个上升段、假平台、下降段和最终平台区。在每种情况下,上升段和假平台都与反应混合物中形成的肝素c-抗凝血酶复合物的浓度密切相关。此外,这两个过程的下降段和最终平台与相应的粘多糖-酶相互作用产物量的增加相吻合。肝素-抗凝血酶复合物中和因子IXa或凝血酶的二级速率常数分别为3.0×10⁸ M⁻¹ min⁻¹和1.7×10⁹ M⁻¹ min⁻¹。肝素-抗凝血酶复合物抑制粘多糖-因子IXa或粘多糖-凝血酶相互作用产物的二级速率常数分别为2.0×10⁷ M⁻¹ min⁻¹和3.0×10⁸ M⁻¹ min⁻¹。这些动力学参数必须与在无粘多糖情况下获得的类似指定常数进行对比,后者分别为2.94×10⁴ M⁻¹ min⁻¹和4.25×10⁵ M⁻¹ min⁻¹。因此,我们的数据表明,蛋白酶抑制剂对凝血酶、因子IXa、因子Xa或纤溶酶的中和速率的粘多糖依赖性增强需要肝素与抗凝血酶结合。此外,对各种常数的仔细比较表明,肝素与抗凝血酶之间的直接相互作用可能在很大程度上导致了这种粘多糖的动力学效应。