Gonzalez-Gronow M, Siefring G E, Castellino F J
J Biol Chem. 1978 Feb 25;253(4):1090-4.
The object of this investigation was to distinguish between two potential mechanisms of activation of human plasminogen (HPg) to plasmin (HPm) by catalytic levels of the activator complex, streptokinase.plasmin (SK.HPm). One mechanism, which is widely supported, postulates an enzymatic role for SK.HPm in the conversion of molar excesses of plasminogen to plasmin. A more recently described kinetic mechanism involves a direct conversion of HPg to HPm by streptokinase (SK). Here, it is believed that displacement of HPm from SK.HPm by excess HPg is the major source of free HPm in the activation process. The present paper shows that SK is not capable of undergoing rapid exchange from SK.HPm to other HPg or HPm molecules, thus precluding the possibility of direct activation of HPg by SK. Our evidence supports a mechanism involving an enzymatic role for SK.HPm as the major means of converting free HPg to HPm.
本研究的目的是区分激活剂复合物链激酶 - 纤溶酶(SK.HPm)在催化水平下将人纤溶酶原(HPg)激活为纤溶酶(HPm)的两种潜在机制。一种得到广泛支持的机制假定SK.HPm在将过量摩尔数的纤溶酶原转化为纤溶酶过程中起酶促作用。最近描述的一种动力学机制涉及链激酶(SK)将HPg直接转化为HPm。在此,人们认为在激活过程中,过量的HPg将HPm从SK.HPm中置换出来是游离HPm的主要来源。本文表明SK不能从SK.HPm快速交换到其他HPg或HPm分子,因此排除了SK直接激活HPg的可能性。我们的证据支持一种机制,即SK.HPm作为将游离HPg转化为HPm的主要方式起酶促作用。