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人血小板上因子VIII/血管性血友病因子特异性结合位点的证实与特性分析

Demonstration and characterization of specific binding sites for factor VIII/von Willebrand factor on human platelets.

作者信息

Kao K J, Pizzo S V, McKee P A

出版信息

J Clin Invest. 1979 Apr;63(4):656-64. doi: 10.1172/JCI109348.

Abstract

The presence of specific Factor VIII/von Willebrand factor (FVIII/vWF) binding sites on human platelets has been demonstrated by using 125I-FVIII/vWF and washed human platelets. Binding is ristocetin-dependent and increases in proportion to the concentration of ristocetin from 0.2 to 1 mg/ml. Binding of 125I-FVIII/vWF to platelets can be competitively inhibited by unlabeled human or bovine FVIII/vWF, but not by human thrombin, fibrinogen, alpha 2-macroglobulin, equine collagen, or a lectin of Ricinus communis. Scatchard analysis of binding data indicated that the dissociation constant of FVIII/vWF receptors is 0.45--0.5 nM. There are 31,000 binding sites per platelet at 1 mg/ml of ristocetin concentration. The optimal pH range for binding is from 7.0 to 7.5. At a concentration of 2 mM, EGTA inhibits 86% of the binding; however, 20 mM of Ca++, Mg++, or EDTA have little effect. Binding sites for FVIII/vWF were found only on platelets, and no significant binding was detected with human erythrocytes or polymorphonuclear leukocytes.

摘要

通过使用125I - FVIII/vWF和洗涤过的人血小板,已证明人血小板上存在特定的凝血因子VIII/血管性血友病因子(FVIII/vWF)结合位点。结合是瑞斯托菌素依赖性的,并且与瑞斯托菌素浓度从0.2至1mg/ml成比例增加。125I - FVIII/vWF与血小板的结合可被未标记的人或牛FVIII/vWF竞争性抑制,但不能被人凝血酶、纤维蛋白原、α2 -巨球蛋白、马胶原或蓖麻凝集素抑制。对结合数据的Scatchard分析表明,FVIII/vWF受体的解离常数为0.45 - 0.5 nM。在1mg/ml的瑞斯托菌素浓度下,每个血小板有31,000个结合位点。结合的最佳pH范围是7.0至7.5。在2mM的浓度下,EGTA抑制86%的结合;然而,20mM的Ca++、Mg++或EDTA几乎没有影响。FVIII/vWF的结合位点仅在血小板上发现,在人红细胞或多形核白细胞上未检测到明显结合。

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The effects of various lectins on platelet aggregation and release.各种凝集素对血小板聚集和释放的影响。
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