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- W4387454755 abstract "Abstract G protein-coupled receptors are important drug targets that engage and activate signaling transducers in multiple cellular compartments. Delineating therapeutic signaling from signaling associated with adverse events is an important step towards rational drug design. The glucagon-like peptide-1 receptor (GLP-1R) is a validated target for the treatment of diabetes and obesity, but drugs that target this receptor are a frequent cause of adverse events. Using recently developed biosensors, we explored the ability of GLP-1R to activate 15 pathways in 4 cellular compartments and demonstrate that modifications aimed at improving the therapeutic potential of GLP-1R agonists greatly influence compound efficacy, potency, and safety in a pathway- and compartment-selective manner. These findings, together with comparative structure analysis, time-lapse microscopy, and phosphoproteomics, reveal unique signaling signatures for GLP-1R agonists at the level of receptor conformation, functional selectivity, and location bias, thus associating signaling neighborhoods with functionally distinct cellular outcomes and clinical consequences." @default.
- W4387454755 created "2023-10-10" @default.
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- W4387454755 date "2023-10-09" @default.
- W4387454755 modified "2023-10-13" @default.
- W4387454755 title "GLP-1R signaling neighborhoods associate with the susceptibility to adverse drug reactions of incretin mimetics" @default.
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- W4387454755 doi "https://doi.org/10.1038/s41467-023-41893-4" @default.
- W4387454755 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/37813859" @default.
- W4387454755 hasPublicationYear "2023" @default.