Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor

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Abstract

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.

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Zhao, L. H., Lin, J., Ji, S. Y., Zhou, X. E., Mao, C., Shen, D. D., … Xu, H. E. (2022). Structure insights into selective coupling of G protein subtypes by a class B G protein-coupled receptor. Nature Communications, 13(1). https://doi.org/10.1038/s41467-022-33851-3

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