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Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
G protein-coupled receptor endocytosis generates spatiotemporal bias in β-arrestin signaling.
Sci. Signal. 17:eadi0934 (2024)
The stabilization of different active conformations of G protein-coupled receptors is thought to underlie the varying efficacies of biased and balanced agonists. Here, profiling the activation of signal transducers by angiotensin II type 1 receptor (AT1R) agonists revealed that the extent and kinetics of β-arrestin binding exhibited substantial ligand-dependent differences, which were lost when receptor internalization was inhibited. When AT1R endocytosis was prevented, even weak partial agonists of the β-arrestin pathway acted as full or near-full agonists, suggesting that receptor conformation did not exclusively determine β-arrestin recruitment. The ligand-dependent variance in β-arrestin translocation was much larger at endosomes than at the plasma membrane, showing that ligand efficacy in the β-arrestin pathway was spatiotemporally determined. Experimental investigations and mathematical modeling demonstrated how multiple factors concurrently shaped the effects of agonists on endosomal receptor-β-arrestin binding and thus determined the extent of functional selectivity. Ligand dissociation rate and G protein activity had particularly strong, internalization-dependent effects on the receptor-β-arrestin interaction. We also showed that endocytosis regulated the agonist efficacies of two other receptors with sustained β-arrestin binding: the V2 vasopressin receptor and a mutant β2-adrenergic receptor. In the absence of endocytosis, the agonist-dependent variance in β-arrestin2 binding was markedly diminished. Our results suggest that endocytosis determines the spatiotemporal bias in GPCR signaling and can aid in the development of more efficacious, functionally selective compounds.
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Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Phosphatidylinositol 4-phosphate; Functional Selectivity; Mediated Endocytosis; Angiotensin; Phosphorylation; Activation; Agonist; Dephosphorylation; Sequestration; Clathrin
ISSN (print) / ISBN
1945-0877
e-ISSN
1937-9145
Zeitschrift
Science Signaling
Quellenangaben
Band: 17,
Heft: 842,
Artikelnummer: eadi0934
Verlag
American Association for the Advancement of Science (AAAS)
Verlagsort
1200 New York Ave, Nw, Washington, Dc 20005 Usa
Nichtpatentliteratur
Publikationen
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Computational Biology (ICB)
Förderungen
Japan Agency for Medical Research and Development
Ministry for National Economy
Janos Bolyai Research Scholarship
Janos Bolyai Research Scholarship Plus of the Hungarian Academy of Sciences
Japan Society for the Promotion of Science
Japan Science and Technology Agency
Hungarian National Research, Development and innovation Fund
Ministry for National Economy
Janos Bolyai Research Scholarship
Janos Bolyai Research Scholarship Plus of the Hungarian Academy of Sciences
Japan Society for the Promotion of Science
Japan Science and Technology Agency
Hungarian National Research, Development and innovation Fund