Institute of Biochemistry and Molecular Biology, ZBMZ, Faculty of Medicine, University of Freiburg, Germany.
Faculty of Biology, University of Freiburg, Germany.
FEBS Lett. 2021 Apr;595(8):1205-1222. doi: 10.1002/1873-3468.14039. Epub 2021 Feb 3.
Mitochondria contain more than 1000 different proteins, including several proteolytic enzymes. These mitochondrial proteases form a complex system that performs limited and terminal proteolysis to build the mitochondrial proteome, maintain, and control its functions or degrade mitochondrial proteins and peptides. During protein biogenesis, presequence proteases cleave and degrade mitochondrial targeting signals to obtain mature functional proteins. Processing by proteases also exerts a regulatory role in modulation of mitochondrial functions and quality control enzymes degrade misfolded, aged, or superfluous proteins. Depending on their different functions and substrates, defects in mitochondrial proteases can affect the majority of the mitochondrial proteome or only a single protein. Consequently, mutations in mitochondrial proteases have been linked to several human diseases. This review gives an overview of the components and functions of the mitochondrial proteolytic machinery and highlights the pathological consequences of dysfunctional mitochondrial protein processing and turnover.
线粒体含有超过 1000 种不同的蛋白质,包括几种蛋白水解酶。这些线粒体蛋白酶形成了一个复杂的系统,进行有限的和末端的蛋白水解,以构建线粒体蛋白质组,维持和控制其功能,或降解线粒体蛋白质和肽。在蛋白质生物发生过程中,前导序列蛋白酶切割和降解线粒体靶向信号以获得成熟的功能性蛋白质。蛋白酶的加工也在调节线粒体功能和质量控制酶降解错误折叠、老化或多余的蛋白质中发挥调节作用。根据它们不同的功能和底物,线粒体蛋白酶的缺陷会影响大多数线粒体蛋白质组或仅单个蛋白质。因此,线粒体蛋白酶的突变与几种人类疾病有关。本综述概述了线粒体蛋白水解机制的组成和功能,并强调了功能失调的线粒体蛋白加工和周转的病理后果。