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Structure of the human respiratory complex II.
Du, Zhanqiang; Zhou, Xiaoting; Lai, Yuezheng; Xu, Jinxu; Zhang, Yuying; Zhou, Shan; Feng, Ziyan; Yu, Long; Tang, Yanting; Wang, Weiwei; Yu, Lu; Tian, Changlin; Ran, Ting; Chen, Hongming; Guddat, Luke W; Liu, Fengjiang; Gao, Yan; Rao, Zihe; Gong, Hongri.
Afiliação
  • Du Z; State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China.
  • Zhou X; State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock, School of Life Sciences, Inner Mongolia University, Hohhot 010070, China.
  • Lai Y; State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China.
  • Xu J; State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China.
  • Zhang Y; State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China.
  • Zhou S; State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China.
  • Feng Z; State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China.
  • Yu L; State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China.
  • Tang Y; State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China.
  • Wang W; Shanghai Institute for Advanced Immunochemical Studies and School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
  • Yu L; High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China.
  • Tian C; High Magnetic Field Laboratory, Chinese Academy of Sciences, Hefei 230031, China.
  • Ran T; Innovative Center For Pathogen Research, Guangzhou Laboratory, Guangzhou 510005, China.
  • Chen H; Innovative Center For Pathogen Research, Guangzhou Laboratory, Guangzhou 510005, China.
  • Guddat LW; School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia.
  • Liu F; Innovative Center For Pathogen Research, Guangzhou Laboratory, Guangzhou 510005, China.
  • Gao Y; Shanghai Institute for Advanced Immunochemical Studies and School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
  • Rao Z; State Key Laboratory of Medicinal Chemical Biology, Frontiers Science Center for Cell Responses, College of Life Sciences, Nankai University, Tianjin 300353, China.
  • Gong H; Shanghai Institute for Advanced Immunochemical Studies and School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Proc Natl Acad Sci U S A ; 120(18): e2216713120, 2023 05 02.
Article em En | MEDLINE | ID: mdl-37098072
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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estrutura Quaternária de Proteína Limite: Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Estrutura Quaternária de Proteína Limite: Humans Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos