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Highly multiplexed bioactivity screening reveals human and microbiota metabolome-GPCRome interactions.

Authors :
Chen H
Rosen CE
González-Hernández JA
Song D
Potempa J
Ring AM
Palm NW
Source :
Cell [Cell] 2023 Jul 06; Vol. 186 (14), pp. 3095-3110.e19. Date of Electronic Publication: 2023 Jun 14.
Publication Year :
2023

Abstract

The human body contains thousands of metabolites derived from mammalian cells, the microbiota, food, and medical drugs. Many bioactive metabolites act through the engagement of G-protein-coupled receptors (GPCRs); however, technological limitations constrain current explorations of metabolite-GPCR interactions. Here, we developed a highly multiplexed screening technology called PRESTO-Salsa that enables simultaneous assessment of nearly all conventional GPCRs (>300 receptors) in a single well of a 96-well plate. Using PRESTO-Salsa, we screened 1,041 human-associated metabolites against the GPCRome and uncovered previously unreported endogenous, exogenous, and microbial GPCR agonists. Next, we leveraged PRESTO-Salsa to generate an atlas of microbiome-GPCR interactions across 435 human microbiome strains from multiple body sites, revealing conserved patterns of cross-tissue GPCR engagement and activation of CD97/ADGRE5 by the Porphyromonas gingivalis protease gingipain K. These studies thus establish a highly multiplexed bioactivity screening technology and expose a diverse landscape of human, diet, drug, and microbiota metabolome-GPCRome interactions.<br />Competing Interests: Declaration of interests N.W.P is a co-founder of Artizan Biosciences and Design Pharmaceuticals. N.W.P has received research funding for unrelated studies from Artizan Biosciences and F. Hoffmann-La Roche AG. H.C., A.M.R., and N.W.P. are inventors on a patent application covering the PRESTO-Salsa system.<br /> (Copyright © 2023 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-4172
Volume :
186
Issue :
14
Database :
MEDLINE
Journal :
Cell
Publication Type :
Academic Journal
Accession number :
37321219
Full Text :
https://doi.org/10.1016/j.cell.2023.05.024