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Article: Biased Coupling to β-Arrestin of Two Common Variants of the CB

Turu, Gábor / Soltész-Katona, Eszter / Tóth, András Dávid / Juhász, Cintia / Cserző, Miklós / Misák, Ádám / Balla, András / Caron, Marc G / Hunyady, László

Frontiers in endocrinology

2021  Volume 12, Page(s) 714561

Abstract: β-arrestins are partners of the G protein-coupled receptors (GPCRs), regulating their intracellular trafficking and signaling. Development of biased GPCR agonists, selectively targeting either G protein or β-arrestin pathways, are in the focus of ... ...

Abstract β-arrestins are partners of the G protein-coupled receptors (GPCRs), regulating their intracellular trafficking and signaling. Development of biased GPCR agonists, selectively targeting either G protein or β-arrestin pathways, are in the focus of interest due to their therapeutic potential in different pathological conditions. The CB
MeSH term(s) HEK293 Cells ; Humans ; Mutation, Missense ; Protein Binding ; Protein Transport ; Receptor, Cannabinoid, CB2/chemistry ; Receptor, Cannabinoid, CB2/genetics ; Receptor, Cannabinoid, CB2/metabolism ; beta-Arrestins/genetics ; beta-Arrestins/metabolism
Chemical Substances Receptor, Cannabinoid, CB2 ; beta-Arrestins
Language English
Publishing date 2021-08-16
Publishing country Switzerland
Document type Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 2592084-4
ISSN 1664-2392
ISSN 1664-2392
DOI 10.3389/fendo.2021.714561
Database MEDical Literature Analysis and Retrieval System OnLINE

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