Lee P P, Wohl R C, Boreisha I G, Robbins K C
Department of Medicine, University of Chicago Medical Center/Michael Reese Hospital and Medical Center, Pritzker School of Medicine, University of Chicago, Illinois 60616.
Biochemistry. 1988 Sep 20;27(19):7506-13. doi: 10.1021/bi00419a049.
The kinetic parameters of three activator species of Glu1-plasminogen (Glu1-Plg) were compared in their reaction at pH 7.4 and 37 degrees C, in the presence and absence of CNBr-digested fibrinogen (CNBr-Fg). The urokinase- (u-PA-) derived covalent hybrid activator PlnA-u-PAB had an apparent Michaelis constant (Kplg) of 7.44 microM, a catalytic rate constant (kplg) of 51.1 min-1, and a second-order rate constant (kplg/Kplg) of 6.87 microM-1 min-1. The tissue plasminogen activator (t-PA) derived covalent hybrid activator PlnA-t-PAB was characterized by a Kplg of 3.33 microM, a kplg of 1.03 min-1, and a kplg/Kplg of 0.309 microM-1 min-1. The kplg/Kplg values for the parent u-PA and t-PA activators were 6- and 16-fold higher than the respective hybrids, mainly due to an approximately 10-fold increase in the apparent Kplg for the hybrids. In the presence of CNBr-Fg, the increase of the kplg/Kplg values for u-PA and its hybrid was 1.1-fold, but for t-PA and its hybrid, the increases were 7- and 12-fold, respectively. In both the absence and presence of CNBr-Fg, activator t-PAB had an apparent Kplg of 19.1 and 27.6 microM and a kplg of 2.9 and 5.0 min-1, respectively. The increase in the kplg/Kplg value with CNBr-Fg was 1.2-fold. The streptokinase- (SK-) derived activators Glu1-plasmin.SK (Glu1-Pln.SK), Val442-Pln.SK, and Val561-Pln.SK had apparent Kplg values of 0.458, 0.268, and 0.121 microM and kplg values of 20.0, 126.0, and 63.3 min-1, respectively. In the presence of CNBr-Fg, the first two activators showed an approximately 1.4-fold increase and the last showed a 1.4-fold decrease in their kplg/Kplg values. The catalytic efficiency (kplg/Kplg) of the various activator species fell in the decreasing order SK greater than u-PA greater than t-PA, in either the presence or absence of CNBr-Fg. CNBr-Fg enhanced significantly the activities of only two activators, t-PA and PlnA-t-PAB.
在pH 7.4和37℃条件下,比较了三种谷氨酸1 - 纤溶酶原(Glu1 - Plg)激活剂在有无CNBr消化的纤维蛋白原(CNBr - Fg)存在时的反应动力学参数。尿激酶(u - PA)衍生的共价杂交激活剂PlnA - u - PAB的表观米氏常数(Kplg)为7.44微摩尔,催化速率常数(kplg)为51.1分钟⁻¹,二级速率常数(kplg/Kplg)为6.87微摩尔⁻¹分钟⁻¹。组织纤溶酶原激活剂(t - PA)衍生的共价杂交激活剂PlnA - t - PAB的特征在于Kplg为3.33微摩尔,kplg为1.03分钟⁻¹,kplg/Kplg为0.309微摩尔⁻¹分钟⁻¹。亲本u - PA和t - PA激活剂的kplg/Kplg值分别比各自的杂交体高6倍和16倍,主要是因为杂交体的表观Kplg增加了约10倍。在存在CNBr - Fg的情况下,u - PA及其杂交体的kplg/Kplg值增加了1.1倍,但t - PA及其杂交体的增加分别为7倍和12倍。在不存在和存在CNBr - Fg的情况下,激活剂t - PAB的表观Kplg分别为19.1和27.6微摩尔,kplg分别为2.9和5.0分钟⁻¹。CNBr - Fg存在时kplg/Kplg值的增加为1.2倍。链激酶(SK)衍生的激活剂谷氨酸1 - 纤溶酶.SK(Glu1 - Pln.SK)、缬氨酸44处的纤溶酶.SK(Val442 - Pln.SK)和缬氨酸561处的纤溶酶.SK(Val