首页> 美国卫生研究院文献>The Journal of Clinical Investigation >Serum prostacyclin stabilizing factor is identical to apolipoprotein A-I (Apo A-I). A novel function of Apo A-I.
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Serum prostacyclin stabilizing factor is identical to apolipoprotein A-I (Apo A-I). A novel function of Apo A-I.

机译:血清前列环素稳定因子与载脂蛋白A-I(Apo A-I)相同。 Apo A-I的新功能。

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摘要

Serum PGI2 stabilizing factor (PSF) was purified from human serum to a single protein with a molecular weight of 28,000 D by SDS-PAGE. Analyses of NH2-terminal sequence (32 residues), COOH-terminal sequence (3 residues) and the composition of amino acids disclosed its homology with human apolipoprotein A-I (Apo A-I), a major apolipoprotein of HDL. Apolipoprotein A-II, C-I, C-II, C-III, D and E, as well as LDL, and VLDL did not possess this activity. The alpha-helix structure of Apo A-I is necessary for the binding of PGI2. HDL and nascent HDL reconstituted from Apo A-I and phospholipid significantly prolonged the half-life of PGI2. PGI2 stabilization by HDL and Apo A-I may be an important protective action against the accumulation of platelet thrombi at sites of vascular damage. The beneficial effect of HDL in the prevention of coronary artery disease may be partly due to this action.
机译:通过SDS-PAGE将血清PGI2稳定因子(PSF)从人血清中纯化为分子量为28,000 D的单一蛋白质。 NH2-末端序列(32个残基),COOH-末端序列(3个残基)的分析和氨基酸组成揭示了其与人载脂蛋白A-I(Apo A-I)的同源性,后者是HDL的主要载脂蛋白。载脂蛋白A-II,C-1,C-II,C-III,D和E以及LDL和VLDL不具有此活性。 Apo A-1的α-螺旋结构对于结合PGI2是必需的。由Apo A-1和磷脂重构的HDL和新生HDL显着延长了PGI2的半衰期。 HDL和Apo A-I对PGI2的稳定作用可能是针对血管损伤部位血小板血栓积聚的重要保护作用。 HDL预防冠状动脉疾病的有益作用可能部分是由于此作用。

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