Weisgraber K H
Gladstone Foundation Laboratories for Cardiovascular Disease, Department of Pathology, University of California, San Francisco 94140-0608.
J Lipid Res. 1990 Aug;31(8):1503-11.
Human apolipoprotein (apo) E occurs as three common isoforms (apoE4, E3, and E2), all of which influence plasma cholesterol levels. Although both apoE4 and E3 bind with equal effectiveness to the low density lipoprotein receptor, they associate preferentially with different classes of plasma lipoproteins: apoE4 with very low density lipoproteins, apoE3 with high density lipoproteins. The primary structure of apoE3 differs from that of apoE4 at only a single site; apoE3 has its sole cysteine residue at position 112, while apoE4 contains arginine at position 112 and completely lacks cysteine. The present study investigated how this structural difference between apoE4 and E3 determines their distribution among plasma lipoproteins, and analyzed the role of the disulfide-linked heterodimer apoE-A-II (which apoE4 cannot form) in determining the distribution. Human plasma was incubated with 125I-labeled apoE, and lipoproteins were separated by agarose chromatography. Both apoE3 that had been reduced and alkylated with iodoacetamide and apoE3-A-II distributed with high density lipoproteins, indicating that a combination of an inherent property of the monomeric apoE3 structure and apoE-A-II formation account for distribution of apoE3 to the high density lipoproteins. Cysteamine modification of apoE3 resulted in an apoE4-like distribution, demonstrating that a positive charge at position 112 determined the apoE4 distribution and that the effect was not exclusively due to the presence of arginine at this position.(ABSTRACT TRUNCATED AT 250 WORDS)
人类载脂蛋白(apo)E有三种常见的异构体(apoE4、E3和E2),它们都会影响血浆胆固醇水平。尽管apoE4和E3与低密度脂蛋白受体的结合效率相同,但它们优先与不同类型的血浆脂蛋白结合:apoE4与极低密度脂蛋白结合,apoE3与高密度脂蛋白结合。apoE3的一级结构与apoE4仅在一个位点不同;apoE3在第112位有唯一的半胱氨酸残基,而apoE4在第112位含有精氨酸且完全没有半胱氨酸。本研究调查了apoE4和E3之间的这种结构差异如何决定它们在血浆脂蛋白中的分布,并分析了二硫键连接的异二聚体apoE-A-II(apoE4无法形成)在决定分布中的作用。将人血浆与125I标记的apoE一起孵育,然后通过琼脂糖色谱法分离脂蛋白。用碘乙酰胺还原和烷基化的apoE3以及apoE3-A-II都与高密度脂蛋白一起分布,这表明单体apoE3结构的固有特性和apoE-A-II的形成共同导致了apoE3向高密度脂蛋白的分布。apoE3的半胱胺修饰导致了类似apoE4的分布,这表明第112位的正电荷决定了apoE4的分布,而且这种作用并非仅仅是由于该位置存在精氨酸。(摘要截短至250字)