Mirkamalova E G, Baskova I P
Biokhimiia. 1978 Nov;43(11):1939-53.
The review of different mechanisms of non-physiological non-specific prothrombin activation is given as compared with the specific activation by the factor Xa. The use of snake venom enzymes or staphylocoagulase makes possible the thrombin generation from pathological forms of prothrombin lacking of gamma-carboxyglutamic acid and incapable of complete activation into thrombin by the specific activator, factor Xa. This fact stimulated the use of non-specific activators in medicine. Investigation of non-specific prothrombin activators made possible to reveal and to trace pathways of the formation of thrombin active site. It is demonstrated that prothrombin, like other serine proenzymes (trypsinogen, chymotrypsinogen), has already formed active site. This site can be revealed under changes of the conformation of the prothrombin molecule due to the chemical modification or the complex formation with staphylocoagulase.
与凝血因子Xa的特异性激活相比,本文综述了非生理性非特异性凝血酶原激活的不同机制。使用蛇毒酶或葡萄球菌凝固酶可从缺乏γ-羧基谷氨酸且无法被特异性激活剂凝血因子Xa完全激活为凝血酶的病理性凝血酶原形式生成凝血酶。这一事实推动了非特异性激活剂在医学中的应用。对非特异性凝血酶原激活剂的研究使得揭示和追踪凝血酶活性位点的形成途径成为可能。结果表明,凝血酶与其他丝氨酸前酶(胰蛋白酶原、糜蛋白酶原)一样,已经形成了活性位点。由于化学修饰或与葡萄球菌凝固酶形成复合物导致凝血酶原分子构象发生变化时,该位点可被揭示。