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- W4384693802 abstract "Transduction (ERNEST COST Action). The papers tackled various aspects of GPCR research. 17The study by Pawnikar and Miao [1] focused on the search for peptides capable of activating CXCR4 18 chemokine receptor by developing a method that used a novel Peptide Gaussian accelerated molecular 19 dynamics (Pep-GaMD) approach to explore representative binding conformations of each peptide and 20 identify critical low-energy states of CXCR4 activated by the super versus partial peptide agonists. 21The study by Saecker et al. [2] dealt with a different relevant aspect of GPCR research, namely the 22 recruitment of arrestins following the interaction of a GPCR with an agonist. Specifically, the authors 23 developed a live cell assay for adenosine A1 receptor (A1AR)-mediated β-arrestin 2 recruitment based 24 on NanoBit® technology. The assay characterized a set of partial and full A1AR agonists with highly 25 reproducible results and an excellent signal-to-noise ratio. 26The study by Ma et al. [3] pursued the development of a fluorescent probe for GPR120, a potential 27 target for many physiological diseases, including type 2 diabetes mellitus. The authors identified 28 compound D5 as a potent GPR120 agonist with high activity and selectivity in vitro and a significant 29 glucose-lowering effect in vivo. 30Finally, the review article by Farooq et" @default.
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- W4384693802 date "2023-07-18" @default.
- W4384693802 modified "2023-10-14" @default.
- W4384693802 title "Editorial: Molecular modulators of GPCRs signal transduction" @default.
- W4384693802 doi "https://doi.org/10.3389/fendo.2023.1252734" @default.
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