Structure of the human respiratory complex II

Author:

Du Zhanqiang1ORCID,Zhou Xiaoting2,Lai Yuezheng1,Xu Jinxu1,Zhang Yuying1ORCID,Zhou Shan1,Feng Ziyan1,Yu Long1,Tang Yanting1ORCID,Wang Weiwei3,Yu Lu4ORCID,Tian Changlin4,Ran Ting5,Chen Hongming5,Guddat Luke W.6ORCID,Liu Fengjiang5,Gao Yan3ORCID,Rao Zihe13678ORCID,Gong Hongri1ORCID

Affiliation:

1. State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China

2. State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot 010070, China

3. Shanghai Institute for Advanced Immunochemical Studies and School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.

4. High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China

5. Innovative Center For Pathogen Research, Guangzhou Laboratory, Guangzhou 510005, China

6. School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia

7. National Laboratory of Biomacromolecules, CAS Center for Excellence in Biomacromolecules, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China

8. Laboratory of Structural Biology, Tsinghua University, Beijing 100084, China

Abstract

Human complex II is a key protein complex that links two essential energy-producing processes: the tricarboxylic acid cycle and oxidative phosphorylation. Deficiencies due to mutagenesis have been shown to cause mitochondrial disease and some types of cancers. However, the structure of this complex is yet to be resolved, hindering a comprehensive understanding of the functional aspects of this molecular machine. Here, we have determined the structure of human complex II in the presence of ubiquinone at 2.86 Å resolution by cryoelectron microscopy, showing it comprises two water-soluble subunits, SDHA and SDHB, and two membrane-spanning subunits, SDHC and SDHD. This structure allows us to propose a route for electron transfer. In addition, clinically relevant mutations are mapped onto the structure. This mapping provides a molecular understanding to explain why these variants have the potential to produce disease.

Funder

MOST | National Key Research and Development Program of China Stem Cell and Translational Research

MOST | National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Cited by 13 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3