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冷冻电镜下的哺乳动物呼吸链复合物 I

Mammalian Respiratory Complex I Through the Lens of Cryo-EM.

机构信息

Medical Research Council Mitochondrial Biology Unit, University of Cambridge, Cambridge CB2 0XY, United Kingdom; email:

Current affiliation: York Structural Biology Laboratory, Department of Chemistry, University of York, York YO10 5DD, United Kingdom.

出版信息

Annu Rev Biophys. 2019 May 6;48:165-184. doi: 10.1146/annurev-biophys-052118-115704. Epub 2019 Feb 20.

Abstract

Single-particle electron cryomicroscopy (cryo-EM) has led to a revolution in structural work on mammalian respiratory complex I. Complex I (mitochondrial NADH:ubiquinone oxidoreductase), a membrane-bound redox-driven proton pump, is one of the largest and most complicated enzymes in the mammalian cell. Rapid progress, following the first 5-Å resolution data on bovine complex I in 2014, has led to a model for mouse complex I at 3.3-Å resolution that contains 96% of the 8,518 residues and to the identification of different particle classes, some of which are assigned to biochemically defined states. Factors that helped improve resolution, including improvements to biochemistry, cryo-EM grid preparation, data collection strategy, and image processing, are discussed. Together with recent structural data from an ancient relative, membrane-bound hydrogenase, cryo-EM on mammalian complex I has provided new insights into the proton-pumping machinery and a foundation for understanding the enzyme's catalytic mechanism.

摘要

单颗粒电子冷冻显微镜(cryo-EM)技术在哺乳动物呼吸复合物 I 的结构研究方面引发了一场革命。复合物 I(线粒体 NADH:泛醌氧化还原酶)是一种膜结合的氧化还原驱动质子泵,是哺乳动物细胞中最大、最复杂的酶之一。自 2014 年首次获得牛复合物 I 的 5-Å 分辨率数据以来,该领域取得了快速进展,目前已获得了分辨率为 3.3-Å 的小鼠复合物 I 模型,该模型包含 8518 个残基中的 96%,并鉴定出不同的颗粒类别,其中一些被分配到生物化学定义的状态。本文讨论了有助于提高分辨率的因素,包括生化、cryo-EM 网格制备、数据收集策略和图像处理方面的改进。结合来自古老亲缘体的膜结合氢化酶的最新结构数据,cryo-EM 技术为质子泵机制提供了新的见解,并为理解该酶的催化机制奠定了基础。

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