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通过密度梯度离心法分离哺乳动物过氧化物酶体。

Isolation of Mammalian Peroxisomes by Density Gradient Centrifugation.

机构信息

Institute of Neuroanatomy, Medical Faculty Mannheim, Mannheim Centre for Translational Neuroscience, Mannheim, Germany.

出版信息

Methods Mol Biol. 2023;2643:1-12. doi: 10.1007/978-1-0716-3048-8_1.

Abstract

Sophisticated organelle fractionation strategies were the workhorse of early peroxisome research and led to the characterization of the principal functions of the organelle. However, even in the era of molecular biology and "omics" technologies, they are still of importance to unravel peroxisome-specific proteomes, confirm the localization of still uncharacterized proteins, analyze peroxisome metabolism or lipid composition, or study their protein import mechanism. To isolate and analyze peroxisomes for these purposes, density gradient centrifugation still represents a highly reliable and reproducible technique. This article describes two protocols to purify peroxisomes from either liver tissue or the HepG2 hepatoma cell line. The protocol for liver enables purification of peroxisome fractions with high purity (95%) and is therefore suitable to study low-abundant peroxisomal proteins or analyze their lipid composition, for example. The protocol presented for HepG2 cells is not suitable to gain highly pure peroxisomal fractions but is intended to be used for gradient profiling experiments and allows easier manipulation of the peroxisomal compartment, e.g., by gene knockdown or protein overexpression for functional studies. Both purification methods therefore represent complementary tools to be used to analyze different aspects of peroxisome physiology. Please note that this is an updated version of a protocol, which has been published in a former volume of Methods in Molecular Biology.

摘要

复杂的细胞器分离策略是早期过氧化物酶体研究的主要手段,有助于确定细胞器的主要功能。然而,即使在分子生物学和“组学”技术时代,它们对于揭示过氧化物酶体特异性蛋白质组、确认尚未鉴定的蛋白质的定位、分析过氧化物酶体代谢或脂质组成,或研究其蛋白质导入机制仍然很重要。为了达到这些目的而分离和分析过氧化物酶体,密度梯度离心仍然是一种高度可靠和可重复的技术。本文描述了两种从肝组织或 HepG2 肝癌细胞系中纯化过氧化物酶体的方案。用于肝脏的方案能够以高纯度(95%)纯化过氧化物酶体级分,因此适用于研究低丰度过氧化物酶体蛋白质或分析其脂质组成等。为 HepG2 细胞提供的方案不适合获得高度纯净的过氧化物酶体级分,但旨在用于梯度分析实验,并允许更容易地操纵过氧化物酶体区室,例如通过基因敲低或蛋白质过表达进行功能研究。因此,这两种纯化方法是分析过氧化物体生理学不同方面的互补工具。请注意,这是方法分子生物学前一版本中发表的协议的更新版本。

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