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培养的哺乳动物细胞的线粒体:II. 外源蛋白在固定细胞和活细胞中的表达与可视化

The mitochondria of cultured mammalian cells: II. Expression and visualization of exogenous proteins in fixed and live cells.

作者信息

Goffart Steffi, Martinsson Peter, Malka Florence, Rojo Manuel, Spelbrink Johannes N

机构信息

FinMIT Centre of Excellence, Institute of Medical Technology and Tampere University Hospital, University of Tampere, Finland.

出版信息

Methods Mol Biol. 2007;372:17-32. doi: 10.1007/978-1-59745-365-3_2.

Abstract

Mitochondria are almost ubiquitous organelles in Eukaryota. They are highly dynamic and often complex structures in the cell. The mammalian mitochondrial proteome is predicted to comprise as many as 2000-2500 different proteins. Determination of the subcellular localization of any newly identified protein is one of the first steps toward unraveling its biological function. For most mitochondrial proteins, this can now be done relatively easily by cloning a complementary deoxyribonucleic acid of interest in frame with an additional sequence for a fluorescent or nonfluorescent protein tag. Transfection and subsequent visualization, either by direct fluorescence microscopy or by indirect immunofluorescence microscopy, will give the first clue to mitochondrial localization. In combination with a fluorescent "marker" dye, the mitochondrial localization can be confirmed. This chapter describes some of the methods used in determining mitochondrial protein localization, which can also be used to study dynamics of mitochondria or individual mitochondrial proteins or protein complexes.

摘要

线粒体是真核生物中几乎普遍存在的细胞器。它们在细胞中高度动态且结构往往复杂。据预测,哺乳动物的线粒体蛋白质组包含多达2000 - 2500种不同的蛋白质。确定任何新鉴定蛋白质的亚细胞定位是阐明其生物学功能的首要步骤之一。对于大多数线粒体蛋白质,现在可以通过将感兴趣的互补脱氧核糖核酸与荧光或非荧光蛋白质标签的附加序列进行框内克隆来相对容易地完成。通过直接荧光显微镜或间接免疫荧光显微镜进行转染及随后的可视化,将给出线粒体定位的首个线索。结合荧光“标记”染料,可以确认线粒体定位。本章描述了一些用于确定线粒体蛋白质定位的方法,这些方法也可用于研究线粒体或单个线粒体蛋白质或蛋白质复合物的动态变化。

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