Parry M A, Zhang X C, Bode I
Max-Planck Institute of Biochemistry, Dept for Structural Research, Am Klopferspitz 18a, 82152 Martinsried, Germany.
Trends Biochem Sci. 2000 Feb;25(2):53-9. doi: 10.1016/s0968-0004(99)01521-2.
Plasminogen activation is a key event in the fibrinolytic system that results in the dissolution of blood clots, and also promotes cell migration and tissue remodelling. The recent structure determinations of microplasmin in complex with the bacterial plasminogen activators staphylokinase and streptokinase have provided novel insights into the molecular mechanisms of plasminogen activation and cofactor function. These bacterial proteins are cofactor molecules that contribute to exosite formation and enhance the substrate presentation to the enzyme. At the same time, they modulate the specificity of plasmin towards substrates and inhibitors, making a 'specificity switch' possible.
纤溶酶原激活是纤维蛋白溶解系统中的关键事件,它导致血凝块溶解,还促进细胞迁移和组织重塑。最近关于微纤溶酶与细菌纤溶酶原激活剂葡萄球菌激酶和链激酶复合物的结构测定,为纤溶酶原激活和辅因子功能的分子机制提供了新的见解。这些细菌蛋白是辅因子分子,有助于形成外部位点并增强底物向酶的呈递。同时,它们调节纤溶酶对底物和抑制剂的特异性,使得“特异性转换”成为可能。