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 language | English |
---|---|
Article number | e74107 |
Journal | eLife |
Volume | 11 |
Number of pages | 22 |
ISSN | 2050-084X |
DOIs | |
Publication status | Published - 2022 |
Bibliographical note
Publisher Copyright:© 2022, Hauser et al.
Keywords
- computational biology
- G protein
- GPCR
- human
- pharmacology
- signal transduction
- systems biology