Common coupling map advances GPCR-G protein selectivity

Alexander S. Hauser, Charlotte Avet, Claire Normand, Arturo Mancini, Asuka Inoue, Michel Bouvier, David E. Gloriam

Research output: Contribution to journalJournal articleResearchpeer-review

75 Citations (Scopus)
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Abstract

Two-thirds of human hormones and one-third of clinical drugs act on membrane receptors that couple to G proteins to achieve appropriate functional responses. While G protein transducers from literature are annotated in the Guide to Pharmacology database, two recent large-scale datasets now expand the receptor-G protein 'couplome'. However, these three datasets differ in scope and reported G protein couplings giving different coverage and conclusions on G protein-coupled receptor (GPCR)-G protein signaling. Here, we report a common coupling map uncovering novel couplings supported by both large-scale studies, the selectivity/promiscuity of GPCRs and G proteins, and how the co-coupling and co-expression of G proteins compare to the families from phylogenetic relationships. The coupling map and insights on GPCR-G protein selectivity will catalyze advances in receptor research and cellular signaling toward the exploitation of G protein signaling bias in design of safer drugs.

Original languageEnglish
Article numbere74107
JournaleLife
Volume11
Number of pages22
ISSN2050-084X
DOIs
Publication statusPublished - 2022

Bibliographical note

Publisher Copyright:
© 2022, Hauser et al.

Keywords

  • computational biology
  • G protein
  • GPCR
  • human
  • pharmacology
  • signal transduction
  • systems biology

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