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健康男性低密度脂蛋白中分子量和载脂蛋白的异质性

Heterogeneity of molecular weight and apolipoproteins in low density lipoproteins of healthy human males.

作者信息

Kahlon T S, Shore V G, Lindgren F T

机构信息

Western Regional Research Center, USDA-ARS, Albany, California 94710.

出版信息

Lipids. 1992 Dec;27(12):1055-7. doi: 10.1007/BF02535588.

DOI:10.1007/BF02535588
PMID:1487953
Abstract

The molecular weights of five low density lipoprotein (LDL) subfractions from four normal healthy males were determined by analytic ultracentrifuge sedimentation equilibria. Protein content of each subfraction was determined by elemental CHN analysis, and weights of apoprotein peptides were calculated. Molecular weights in subfractions of increasing density were 2.92 +/- 0.26, 2.94 +/- 0.12, 2.68 +/- 0.09, 2.68 +/- 0.28 and 2.23 +/- 0.22 million Da, and protein weight percentages were 21.05, 21.04, 22.05, 23.10 and 29.10, in subfractions 1, 2, 3, 4 and 5, respectively. Total mean apoprotein weights for respective subfractions were 614 +/- 53, 621 +/- 45, 588 +/- 9, 637 +/- 83 and 645 +/- 62 KDa. In addition to a single apoprotein B-100 (apo B-100) peptide with a mean carbohydrate content of 7.1% and a molecular weight of 550 KDa per LDL particle, there may be one or more apoprotein E peptides of 34 KDa and/or apoprotein C-III of 9 KDa. In addition, subfractions 4 and 5 may contain 3-7% apolipoprotein (a). There is considerable heterogeneity among LDL subfractions as well as within the same fraction from different individuals. This heterogeneity may relate to differences in origin, metabolism and/or atherogenicity as a result of their content of apoproteins other than apo B-100.

摘要

通过分析超速离心沉降平衡法测定了来自四名正常健康男性的五种低密度脂蛋白(LDL)亚组分的分子量。通过元素CHN分析测定每个亚组分的蛋白质含量,并计算载脂蛋白肽的重量。密度递增的亚组分中的分子量分别为292±26、294±12、268±9、268±28和223±22 kDa,蛋白质重量百分比在亚组分1、2、3、4和5中分别为21.05、21.04、22.05、23.10和29.10。各个亚组分的总平均载脂蛋白重量分别为614±53、621±45、588±9、637±83和645±62 kDa。除了每个LDL颗粒平均碳水化合物含量为7.1%、分子量为550 kDa的单一载脂蛋白B-100(apo B-100)肽外,可能还有一种或多种34 kDa的载脂蛋白E肽和/或9 kDa的载脂蛋白C-III。此外,亚组分4和5可能含有3%-7%的载脂蛋白(a)。LDL亚组分之间以及来自不同个体的同一亚组分内存在相当大的异质性。这种异质性可能与它们除apo B-100外的载脂蛋白含量导致的起源、代谢和/或致动脉粥样硬化性差异有关。

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