Laube Eike, Schiller Jonathan, Zickermann Volker, Vonck Janet
Department of Structural Biology, Max Planck Institute of Biophysics, 60438 Frankfurt am Main, Germany.
Institute of Biochemistry II, University Hospital, Goethe University, 60590 Frankfurt am Main, Germany.
Acta Crystallogr D Struct Biol. 2024 Mar 1;80(Pt 3):159-173. doi: 10.1107/S205979832400086X. Epub 2024 Feb 19.
Complex I (proton-pumping NADH:ubiquinone oxidoreductase) is the first component of the mitochondrial respiratory chain. In recent years, high-resolution cryo-EM studies of complex I from various species have greatly enhanced the understanding of the structure and function of this important membrane-protein complex. Less well studied is the structural basis of complex I biogenesis. The assembly of this complex of more than 40 subunits, encoded by nuclear or mitochondrial DNA, is an intricate process that requires at least 20 different assembly factors in humans. These are proteins that are transiently associated with building blocks of the complex and are involved in the assembly process, but are not part of mature complex I. Although the assembly pathways have been studied extensively, there is limited information on the structure and molecular function of the assembly factors. Here, the insights that have been gained into the assembly process using cryo-EM are reviewed.
复合体I(质子泵NADH:泛醌氧化还原酶)是线粒体呼吸链的第一个组成部分。近年来,对来自不同物种的复合体I进行的高分辨率冷冻电镜研究极大地增进了人们对这种重要膜蛋白复合体结构和功能的理解。对复合体I生物发生的结构基础研究较少。这个由核DNA或线粒体DNA编码的、包含40多个亚基的复合体的组装是一个复杂的过程,在人类中至少需要20种不同的组装因子。这些是与复合体构建模块短暂关联并参与组装过程,但不是成熟复合体I一部分的蛋白质。尽管组装途径已得到广泛研究,但关于组装因子的结构和分子功能的信息有限。在此,对利用冷冻电镜在组装过程中获得的见解进行综述。