Swords N A, Mann K G
Department of Biochemistry, College of Medicine, University of Vermont, Burlington 05405.
Arterioscler Thromb. 1993 Nov;13(11):1602-12. doi: 10.1161/01.atv.13.11.1602.
Prothrombinase complex assembly, in real time, on platelets adherent to immobilized von Willebrand Factor (vWf) was examined by total internal reflection fluorescence spectroscopy (TIRFS). Electron microscopy showed that the platelets adhered to vWf in a largely unactivated state and could be activated by thrombin. Antibody binding to glycoprotein (GP) Ib and functional GPIIb-IIIa receptor molecules on adherent platelet membranes monitored by TIRFS also indicated that platelets adhered in a largely unactivated state. Maximal expression of the receptor form of GPIIb-IIIa detected by antibody binding was seen only after thrombin stimulation of the adherent platelets. Antibody binding to GPIb was detected on adherent platelets. A reduction in antibody binding was observed after thrombin stimulation of the platelets, indicating a change in GPIb as a consequence of thrombin stimulation of the platelets. The binding of the protein components of the prothrombinase complex to adherent and thrombin-stimulated adherent platelets was then studied individually. Factor Va bound to adherent and thrombin-stimulated adherent platelets was then studied individually. Factor Va bound to adherent and thrombin-stimulated adherent platelets with an estimated Kd of 58 nmol/L. Minimal factor Xa binding was observed on adherent platelets before thrombin stimulation. Factor Xa binding was, however, readily observed on thrombin-stimulated adherent platelets. This factor Xa binding was not saturable, and no Kd value could be estimated. Direct measurement of prothrombinase complex assembly was demonstrated by using an energy transfer phenomenon between fluorescein-labeled factor Va and rhodamine-labeled factor Xa. Prothrombinase complex assembly was observed on both adherent and thrombin-stimulated adherent platelets. The estimated Kd for the factor Va/factor Xa interaction was 4 nmol/L. TIRFS demonstrated that adherent platelets have the ability to support prothrombinase complex assembly, as shown by a direct energy transfer reaction between fluorescently labeled factors Va and Xa.
通过全内反射荧光光谱法(TIRFS)检测了凝血酶原酶复合物在黏附于固定化血管性血友病因子(vWf)的血小板上的实时组装情况。电子显微镜显示,血小板以基本未活化的状态黏附于vWf,并且可被凝血酶激活。通过TIRFS监测抗体与黏附血小板膜上糖蛋白(GP)Ib和功能性GPIIb - IIIa受体分子的结合,也表明血小板以基本未活化的状态黏附。仅在凝血酶刺激黏附血小板后,通过抗体结合检测到的GPIIb - IIIa受体形式才出现最大表达。在黏附血小板上检测到抗体与GPIb的结合。在凝血酶刺激血小板后,观察到抗体结合减少,表明凝血酶刺激血小板导致GPIb发生变化。然后分别研究了凝血酶原酶复合物的蛋白质成分与黏附及凝血酶刺激的黏附血小板的结合。接着分别研究了因子Va与黏附及凝血酶刺激的黏附血小板的结合。因子Va与黏附及凝血酶刺激的黏附血小板结合,估计解离常数(Kd)为58 nmol/L。在凝血酶刺激之前,在黏附血小板上观察到极少的因子Xa结合。然而,在凝血酶刺激的黏附血小板上很容易观察到因子Xa结合。这种因子Xa结合不饱和,无法估计Kd值。通过使用荧光素标记的因子Va和罗丹明标记的因子Xa之间的能量转移现象,证明了凝血酶原酶复合物组装的直接测量。在黏附及凝血酶刺激的黏附血小板上均观察到凝血酶原酶复合物组装。因子Va/因子Xa相互作用的估计Kd为4 nmol/L。TIRFS表明,黏附血小板具有支持凝血酶原酶复合物组装的能力,如荧光标记的因子Va和Xa之间的直接能量转移反应所示。