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bioRxiv · 10.1101/2025.03.24.645127

A pan-positive allosteric modulator that mediates sustainable GPCR activation

Sun, Q.·He, G.·Xu, X.·Kong, F.·Zhang, S.·Sun, X.·Yan, C.·Liu, X.
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Abstract

Approximately 1/3 of all clinical drugs exert their therapeutic effects by modulating the activity of G protein-coupled receptors (GPCRs). Thus, there is a constant interest in finding novel ways to modulate GPCR activity. In this work, through a newly established Survival Pressure Selection (SPS) method for high-throughput screening of GPCR agonists, we discover that atazanavir functions as an agonist for GPR119. Further studies suggest that atazanavir is capable of activating a number of Family A GPCRs, including the {beta}1 adrenergic receptor ({beta}1AR), the {beta}2 adrenergic receptor ({beta}2AR) and the opoioid receptor (OR). Cryo-EM structures reveal that atazanavir binds to an allosteric pocket near TM6/7 in both GPR119 and the {beta}1AR. Pharmacological studies suggest that atazanavir mediates non-canonical signaling of Family A GPCRs. During this process, G protein and {beta}-arrestin are spatially close, but {beta}-arrestin forms a complex with the receptor and G protein instead of desensitizing G protein signaling, thus resulting in sustained G protein signaling. The work expands the signal transduction modes and pharmacological properties of allosteric modulators for GPCRs and provides a general starting point for developing therapeutics targeting this allosteric site.

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Sun, Q., He, G., Xu, X., Kong, F., Zhang, S., Sun, X., Yan, C., Liu, X.. 2025-03-27. A pan-positive allosteric modulator that mediates sustainable GPCR activation. https://doi.org/10.1101/2025.03.24.645127

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