Using cryo-EM to understand the assembly pathway of respiratory complex I.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-03-01 Epub Date: 2024-02-19 DOI:10.1107/S205979832400086X
Eike Laube, Jonathan Schiller, Volker Zickermann, Janet Vonck
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Abstract

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.

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利用低温电子显微镜了解呼吸复合体 I 的组装途径。
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,对不同物种的复合体 I 进行的高分辨率低温电子显微镜研究大大提高了人们对这一重要膜蛋白复合体的结构和功能的认识。但对复合体 I 生物发生的结构基础研究较少。这一复合体由 40 多个亚基组成,由核或线粒体 DNA 编码,其组装过程错综复杂,在人类中至少需要 20 种不同的组装因子。这些蛋白质与复合体的构件瞬时关联,参与组装过程,但不是成熟复合体 I 的一部分。尽管对组装途径进行了广泛的研究,但有关组装因子的结构和分子功能的信息却很有限。本文回顾了利用低温电子显微镜对组装过程进行的深入研究。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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