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超速离心法分离和分析血浆脂蛋白。

Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation.

机构信息

Department of Molecular Pathology, Interdisciplinary Graduate School of Medicine, University of Yamanashi.

School of Biotechnology and Health Sciences, Wuyi University.

出版信息

J Vis Exp. 2021 Jan 28(167). doi: 10.3791/61790.

Abstract

Analysis of plasma lipoproteins and apolipoproteins is an essential part for the diagnosis of dyslipidemia and studies of lipid metabolism and atherosclerosis. Although there are several methods for analyzing plasma lipoproteins, ultracentrifugation is still one of the most popular and reliable methods. Because of its intact separation procedure, the lipoprotein fractions isolated by this method can be used for analysis of lipoproteins, apolipoproteins, proteomes, and functional study of lipoproteins with cultured cells in vitro. Here, we provide a detailed protocol to isolate seven lipoprotein fractions including VLDL (d<1.006 g/mL), IDL (d=1.02 g/mL), LDLs (d=1.04 and 1.06 g/mL), HDLs (d=1.08, 1.10, and 1.21 g/mL) from rabbit plasma using sequential floating ultracentrifugation. In addition, we introduce the readers how to analyze apolipoproteins such as apoA-I, apoB, and apoE by SDS-PAGE and Western blotting and show representative results of lipoprotein and apolipoprotein profiles using hyperlipidemic rabbit models. This method can become a standard protocol for both clinicians and basic scientists to analyze lipoprotein functions.

摘要

分析血浆脂蛋白和载脂蛋白是诊断血脂异常、研究脂质代谢和动脉粥样硬化的重要组成部分。尽管有几种分析血浆脂蛋白的方法,但超速离心仍然是最受欢迎和可靠的方法之一。由于其完整的分离程序,用这种方法分离的脂蛋白可以用于脂蛋白、载脂蛋白、蛋白质组学分析,以及体外培养细胞的脂蛋白功能研究。在这里,我们提供了一个详细的方案,用于从兔血浆中分离七种脂蛋白,包括 VLDL(d<1.006 g/mL)、IDL(d=1.02 g/mL)、LDLs(d=1.04 和 1.06 g/mL)、HDLs(d=1.08、1.10 和 1.21 g/mL),采用连续漂浮超速离心法。此外,我们还介绍了如何通过 SDS-PAGE 和 Western blot 分析载脂蛋白,如 apoA-I、apoB 和 apoE,并展示了用高脂血症兔模型得到的脂蛋白和载脂蛋白图谱的代表性结果。该方法可以成为临床医生和基础科学家分析脂蛋白功能的标准方案。

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