Rosing J, Zwaal R F, Tans G
J Biol Chem. 1986 Mar 25;261(9):4224-8.
The conversion of prothrombin into thrombin by Factor Xa requires the cleavage of two peptide bonds in prothrombin. Dependent on the order of cleavage, prethrombin 2 or meizothrombin occurs as intermediate. Since prethrombin 2 has as yet been the only observed intermediate, prothrombin activation is generally considered to proceed via prethrombin 2. In this paper we present new methods that allow differentiation between meizothrombin and thrombin formed during the initial phase of prothrombin activation. These methods, which make use of the different reactivities of meizothrombin and thrombin toward fibrinogen and antithrombin III plus heparin, enabled us to show the generation of considerable amounts of meizothrombin during Factor Xa-catalyzed prothrombin activation. Both meizothrombin and thrombin incorporated the active site-directed fluorescent chloromethyl ketone 5-dimethylaminonaphthalene-1-sulfonyl-Glu-Gly-Arg-CH2Cl. Gel electrophoretic analysis of chloromethyl ketone-treated aliquots of prothrombin activation mixtures confirmed meizothrombin formation. These observations demonstrate that prothrombin may also be converted into thrombin via meizothrombin.
凝血因子Xa将凝血酶原转化为凝血酶需要裂解凝血酶原中的两个肽键。根据裂解顺序,凝血酶原2或中凝血酶作为中间体出现。由于凝血酶原2是目前唯一观察到的中间体,凝血酶原激活通常被认为是通过凝血酶原2进行的。在本文中,我们提出了新的方法,可区分中凝血酶和凝血酶原激活初始阶段形成的凝血酶。这些方法利用了中凝血酶和凝血酶对纤维蛋白原以及抗凝血酶III加肝素的不同反应性,使我们能够证明在凝血因子Xa催化的凝血酶原激活过程中会生成大量的中凝血酶。中凝血酶和凝血酶都掺入了活性位点导向的荧光氯甲基酮5-二甲基氨基萘-1-磺酰基-Glu-Gly-Arg-CH2Cl。对凝血酶原激活混合物的氯甲基酮处理等分试样进行凝胶电泳分析,证实了中凝血酶的形成。这些观察结果表明,凝血酶原也可能通过中凝血酶转化为凝血酶。