Priesnitz Chantal, Pfanner Nikolaus, Becker Thomas
Institute of Biochemistry and Molecular Biology, ZBMZ, Faculty of Medicine, University of Freiburg, Freiburg, Germany; Faculty of Biology, University of Freiburg, Freiburg, Germany.
Institute of Biochemistry and Molecular Biology, ZBMZ, Faculty of Medicine, University of Freiburg, Freiburg, Germany; CIBSS Centre for Integrative Biological Signalling Studies, University of Freiburg, Freiburg, Germany.
Methods Cell Biol. 2020;155:45-79. doi: 10.1016/bs.mcb.2019.11.006. Epub 2019 Dec 12.
Mitochondria are deeply integrated into crucial functions of eukaryotic cells, including ATP production via oxidative phosphorylation, biosynthesis of iron-sulfur clusters, amino acids, lipids and heme, signaling pathways, and programmed cell death. The import of about 1000 different proteins that are produced as precursors on cytosolic ribosomes is essential for mitochondrial functions and biogenesis. The translocase of the outer mitochondrial membrane (TOM) forms the entry gate for the vast majority of mitochondrial proteins. Research of the last years has uncovered a complicated network of protein translocases and pathways that sort proteins into the mitochondrial subcompartments: outer and inner membranes, intermembrane space, and matrix. The in vitro import of a large number of different precursor proteins into mitochondria has been a pivotal experimental assay to identify these protein-sorting routes. This experimental set-up enables studies on the kinetics of protein transport into isolated mitochondria, on the processing of precursor proteins, and on their assembly into functional protein machineries. In vitro protein import assays are widely used and are indispensable for research on mitochondrial protein biogenesis.
线粒体深度参与真核细胞的关键功能,包括通过氧化磷酸化产生ATP、铁硫簇、氨基酸、脂质和血红素的生物合成、信号通路以及程序性细胞死亡。约1000种不同蛋白质以前体形式在胞质核糖体上合成,其导入对于线粒体功能和生物发生至关重要。线粒体外膜转位酶(TOM)构成了绝大多数线粒体蛋白质的进入通道。过去几年的研究揭示了一个复杂的蛋白质转位酶和途径网络,这些网络将蛋白质分选到线粒体亚区室:外膜和内膜、膜间隙和基质。大量不同前体蛋白质体外导入线粒体一直是鉴定这些蛋白质分选途径的关键实验方法。这种实验设置能够研究蛋白质转运到分离线粒体中的动力学、前体蛋白质的加工以及它们组装成功能性蛋白质机器的过程。体外蛋白质导入测定法被广泛使用,对于线粒体蛋白质生物发生的研究不可或缺。