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凝血酶原在带正电荷脂质的膜上的非钙依赖性激活。

Calcium-independent activation of prothrombin on membranes with positively charged lipids.

作者信息

Rosing J, Tans G, Speijer H, Zwaal R F

机构信息

Department of Biochemistry, University of Limburg, Maastricht, The Netherlands.

出版信息

Biochemistry. 1988 Dec 13;27(25):9048-55. doi: 10.1021/bi00425a025.

Abstract

The activation of prothrombin by factor Xa is strongly accelerated by negatively charged phospholipids plus calcium ions. In this paper we report that positively charged membranes can also stimulate prothrombin activation provided that the activation reaction is carried out in the absence of calcium ions. Membranes composed of a mixture of phosphatidylcholine (PC) and positively charged lipids like stearylamine, sphingosine, or hexadecyltrimethylammonium bromide caused a more than 1000-fold increase of the rate of prothrombin activation. Prothrombin activation by the factor Xa-factor Va complex was also considerably stimulated by such membranes. Stimulation of prothrombin activation by positively charged membranes was suppressed at high ionic strength. This suggests that electrostatic attraction of negatively charged proteins by positively charged membranes is the major driving force in the association of prothrombin and factor Xa with the lipid surface. Calcium ions strongly inhibited prothrombin activation on vesicles composed of PC and stearylamine (80/20 M/M), which indicates that the regions of prothrombin and/or factor Xa containing gamma-carboxyglutamic acid (gla) are important for the interaction of these proteins with positively charged membranes. The importance of the gla domain was confirmed by the observation that PC/stearylamine vesicles had much less effect on the reactions between proteins that lack gla residues [gla-domainless (des-1-45) prothrombin, prethrombin 1, prethrombin 2, or gla-domainless (des-1-44) factor Xa]. The efficiency of prothrombin and prothrombin derivatives to act as substrate decreased in the order prothrombin greater than des-1-45-prothrombin = prethrombin 1 greater than prethrombin 2, while prothrombin activation by gla-domainless (des-1-44) factor Xa was hardly stimulated by positively charged membranes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

凝血酶原被因子Xa激活的过程会因带负电荷的磷脂和钙离子而显著加速。在本文中我们报告,只要激活反应在无钙离子的情况下进行,带正电荷的膜也能刺激凝血酶原激活。由磷脂酰胆碱(PC)与诸如硬脂胺、鞘氨醇或十六烷基三甲基溴化铵等带正电荷脂质混合组成的膜,能使凝血酶原激活速率提高1000倍以上。因子Xa - 因子Va复合物对凝血酶原的激活也受到此类膜的显著刺激。带正电荷的膜对凝血酶原激活的刺激在高离子强度下会受到抑制。这表明带正电荷的膜对带负电荷蛋白质的静电吸引是凝血酶原和因子Xa与脂质表面结合的主要驱动力。钙离子强烈抑制在由PC和硬脂胺(80/20摩尔/摩尔)组成的囊泡上的凝血酶原激活,这表明凝血酶原和/或因子Xa中含γ - 羧基谷氨酸(gla)的区域对于这些蛋白质与带正电荷膜的相互作用很重要。gla结构域的重要性通过以下观察得到证实:PC/硬脂胺囊泡对缺乏gla残基的蛋白质(无gla结构域的(去1 - 45)凝血酶原、凝血酶原1、凝血酶原2或无gla结构域的(去1 - 44)因子Xa)之间的反应影响小得多。凝血酶原及其衍生物作为底物的效率按以下顺序降低:凝血酶原>去1 - 45 - 凝血酶原 = 凝血酶原1>凝血酶原2, 而无gla结构域的(去1 - 44)因子Xa对凝血酶原的激活几乎不受带正电荷膜的刺激。(摘要截选至250词)

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