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Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor
The ability to couple with multiple G protein subtypes, such as G(s), G(i/o), or G(q/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 com...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637140/ https://www.ncbi.nlm.nih.gov/pubmed/36335102 http://dx.doi.org/10.1038/s41467-022-33851-3 |
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author | 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 |
author_facet | 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 |
author_sort | Zhao, Li-Hua |
collection | PubMed |
description | The ability to couple with multiple G protein subtypes, such as G(s), G(i/o), or G(q/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 G(s) protein, have been determined. However, no structure of class B GPCRs with G(q/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, G(11) and G(o). We compare these structures with the structure of CRF2R in complex with G(s) 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. |
format | Online Article Text |
id | pubmed-9637140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96371402022-11-07 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 Nat Commun Article The ability to couple with multiple G protein subtypes, such as G(s), G(i/o), or G(q/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 G(s) protein, have been determined. However, no structure of class B GPCRs with G(q/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, G(11) and G(o). We compare these structures with the structure of CRF2R in complex with G(s) 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. Nature Publishing Group UK 2022-11-05 /pmc/articles/PMC9637140/ /pubmed/36335102 http://dx.doi.org/10.1038/s41467-022-33851-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article 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 Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor |
title | Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor |
title_full | Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor |
title_fullStr | Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor |
title_full_unstemmed | Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor |
title_short | Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor |
title_sort | structure insights into selective coupling of g protein subtypes by a class b g protein-coupled receptor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9637140/ https://www.ncbi.nlm.nih.gov/pubmed/36335102 http://dx.doi.org/10.1038/s41467-022-33851-3 |
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