Profiling of basal and ligand-dependent GPCR activities by means of a polyvalent cell-based high-throughput platform
Manel Zeghal,
Geneviève Laroche,
Julia Douglas Freitas,
Rebecca Wang and
Patrick M. Giguère ()
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Manel Zeghal: University of Ottawa
Geneviève Laroche: University of Ottawa
Julia Douglas Freitas: University of Ottawa
Rebecca Wang: University of Ottawa
Patrick M. Giguère: University of Ottawa
Nature Communications, 2023, vol. 14, issue 1, 1-18
Abstract:
Abstract Representing the most attractive and successful druggable receptors of the proteome, GPCRs regulate a myriad of physiological and pathophysiological functions. Although over half of present pharmaceuticals target GPCRs, the advancement of drug discovery is hampered by a lack of adequate screening tools, the majority of which are limited to probing agonist-induced G-protein and β-arrestin-2-mediated events as a measure of receptor activation. Here, we develop Tango-Trio, a comprehensive cell-based high-throughput platform comprising cumate-inducible expression of transducers, capable of the parallelized profiling of both basal and agonist-dependent GPCR activities. We capture the functional diversity of GPCRs, reporting β-arrestin-1/2 couplings, selectivities, and receptor internalization signatures across the GPCRome. Moreover, we present the construction of cumate-induced basal activation curves at approximately 200 receptors, including over 50 orphans. Overall, Tango-Trio’s robustness is well-suited for the functional characterization and screening of GPCRs, especially for parallel interrogation, and is a valuable addition to the pharmacological toolbox.
Date: 2023
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Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-39132-x
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DOI: 10.1038/s41467-023-39132-x
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