Suppr超能文献

线粒体外膜蛋白降解的分子途径。

Molecular pathways of mitochondrial outer membrane protein degradation.

机构信息

Peking University-Tsinghua University-National Institute of Biological Sciences Joint Graduate Program, School of Life Sciences, Peking University, Beijing 100871, China.

National Institute of Biological Sciences, Beijing 102206, China.

出版信息

Biochem Soc Trans. 2019 Oct 31;47(5):1437-1447. doi: 10.1042/BST20190275.

Abstract

Mitochondrial outer membrane (MOM) encloses inner compartments of mitochondria and integrates cytoplasmic signals to regulate essential mitochondrial processes, such as protein import, dynamics, metabolism, cell death, etc. A substantial understanding of MOM associated proteostatic stresses and quality control pathways has been obtained in recent years. Six MOM associated protein degradation (MAD) pathways center on three AAA ATPases: Cdc48 in the cytoplasm, Msp1 integral to MOM, and Yme1 integral to the inner membrane. These pathways survey MOM proteome from the cytoplasmic and the inter-membrane space (IMS) sides. They detect and degrade MOM proteins with misfolded cytoplasmic and IMS domains, remove mistargeted tail-anchored proteins, and clear mitochondrial precursor proteins clogged in the TOM import complex. These MOM associated protein quality control pathways collaboratively maintain mitochondrial proteostasis and cell viability.

摘要

线粒体的外膜(MOM)包围着线粒体的内部结构,并整合细胞质信号来调节重要的线粒体过程,如蛋白质的输入、动力学、代谢、细胞死亡等。近年来,人们对与 MOM 相关的蛋白质稳态应激和质量控制途径有了深入的了解。六个与 MOM 相关的蛋白降解(MAD)途径集中在三个 AAA ATP 酶上:细胞质中的 Cdc48、MOM 上的 Msp1 和内膜上的 Yme1。这些途径从细胞质和膜间空间(IMS)两侧检测和降解 MOM 蛋白。它们检测和降解具有错误折叠的细胞质和 IMS 结构域的 MOM 蛋白,去除靶向错误的尾部锚定蛋白,并清除在 TOM 导入复合物中堵塞的线粒体前体蛋白。这些与 MOM 相关的蛋白质质量控制途径协同维持线粒体蛋白质的稳态和细胞活力。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验