Stone S R, Hofsteenge J
Friedrich Miescher-Institut, Basel, Switzerland.
Eur J Biochem. 1987 Dec 1;169(2):373-6. doi: 10.1111/j.1432-1033.1987.tb13622.x.
The effect of heparin on the interaction between thrombin and hirudin has been examined by kinetic methods. Three forms of heparin fractionated on the basis of their affinity for antithrombin III and unfractionated heparin were found to act as noncompetitive inhibitors of the formation of the thrombin-hirudin complex. A three--four fold increase in the dissociation constant of the complex was observed at saturating heparin concentrations. This increase in the dissociation constant was due to a twofold decrease in the rate of association of thrombin and hirudin together with a similar increase in the rate of dissociation of the complex. Implications for the location of the heparin binding site on thrombin and the possible therapeutic use of the hirudin are discussed.
已通过动力学方法研究了肝素对凝血酶与水蛭素之间相互作用的影响。根据其对抗凝血酶III的亲和力进行分级分离得到的三种肝素形式以及未分级的肝素,均被发现可作为凝血酶-水蛭素复合物形成的非竞争性抑制剂。在肝素浓度饱和时,观察到复合物的解离常数增加了三到四倍。解离常数的这种增加是由于凝血酶与水蛭素结合速率降低了两倍,同时复合物解离速率有类似程度的增加。文中还讨论了肝素在凝血酶上结合位点的位置以及水蛭素可能的治疗用途。