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从小鼠组织中分离功能性线粒体和纯线粒体DNA。

Isolation of Functional Mitochondria and Pure mtDNA from Murine Tissues.

作者信息

Rozsivalova Dieu Hien, Popovic Milica, Kaul Harshita, Trifunovic Aleksandra

机构信息

Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD) and Institute for Mitochondrial Diseases and Aging, Medical Faculty, University of Cologne, Cologne, Germany.

出版信息

Methods Mol Biol. 2023;2615:3-16. doi: 10.1007/978-1-0716-2922-2_1.

Abstract

Detailed analysis of mitochondrial function cannot be achieved without good quality preparations of isolated mitochondria. Ideally, the isolation protocol should be quick, while producing a reasonably pure pool of mitochondria that are still intact and coupled. Here, we describe a fast and simple method for the purification of mammalian mitochondria relying on isopycnic density gradient centrifugation. We describe specific steps that should be taken into consideration when functional mitochondria from different tissues should be isolated. This protocol is suitable for the analysis of many aspects of the organelle's structure and function.

摘要

如果没有高质量的分离线粒体制剂,就无法对线粒体功能进行详细分析。理想情况下,分离方案应快速,同时产生相当纯净的线粒体池,这些线粒体仍保持完整且偶联状态。在此,我们描述一种基于等密度梯度离心法的快速且简单的哺乳动物线粒体纯化方法。我们阐述了分离不同组织中有功能的线粒体时应考虑的具体步骤。该方案适用于对该细胞器结构和功能诸多方面的分析。

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