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Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor.
Zhao, Li-Hua; Lin, Jingyu; Ji, Su-Yu; Zhou, X Edward; Mao, Chunyou; Shen, Dan-Dan; He, Xinheng; Xiao, Peng; Sun, Jinpeng; Melcher, Karsten; Zhang, Yan; Yu, Xiao; Xu, H Eric.
Afiliação
  • Zhao LH; The CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China. zhaolihuawendy@simm.ac.cn.
  • Lin J; University of Chinese Academy of Sciences, Beijing, 100049, China. zhaolihuawendy@simm.ac.cn.
  • Ji SY; Department of Physiology, School of Basic Medical Sciences, Shandong University, Jinan, 250012, China.
  • Zhou XE; Department of Biophysics and Pathology of Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310058, China.
  • Mao C; Department of Structural Biology, Van Andel Research Institute, Grand Rapids, MI, 49503, USA.
  • Shen DD; Department of Biophysics and Pathology of Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310058, China.
  • He X; Department of Biophysics and Pathology of Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310058, China.
  • Xiao P; The CAS Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.
  • Sun J; University of Chinese Academy of Sciences, Beijing, 100049, China.
  • Melcher K; Department of Physiology, School of Basic Medical Sciences, Shandong University, Jinan, 250012, China.
  • Zhang Y; Department of Physiology, School of Basic Medical Sciences, Shandong University, Jinan, 250012, China.
  • Yu X; Department of Structural Biology, Van Andel Research Institute, Grand Rapids, MI, 49503, USA.
  • Xu HE; Department of Biophysics and Pathology of Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310058, China. zhang_yan@zju.edu.cn.
Nat Commun ; 13(1): 6670, 2022 11 05.
Article em En | MEDLINE | ID: mdl-36335102
The ability to couple with multiple G protein subtypes, such as Gs, Gi/o, or Gq/11, by a given G protein-coupled receptor (GPCR) is critical for many physiological processes. Over the past few years, the cryo-EM structures for all 15 members of the medically important class B GPCRs, all in complex with Gs protein, have been determined. However, no structure of class B GPCRs with Gq/11 has been solved to date, limiting our understanding of the precise mechanisms of G protein coupling selectivity. Here we report the structures of corticotropin releasing factor receptor 2 (CRF2R) bound to Urocortin 1 (UCN1), coupled with different classes of heterotrimeric G proteins, G11 and Go. We compare these structures with the structure of CRF2R in complex with Gs to uncover the structural differences that determine the selective coupling of G protein subtypes by CRF2R. These results provide important insights into the structural basis for the ability of CRF2R to couple with multiple G protein subtypes.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Heterotriméricas de Ligação ao GTP Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas Heterotriméricas de Ligação ao GTP Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido