Cargando…
Subcellular location defines GPCR signal transduction
Intracellular G protein-coupled receptors (GPCRs) can be activated by permeant ligands, which contributes to agonist selectivity. Opioid receptors (ORs) provide a notable example, where opioid drugs rapidly activate ORs in the Golgi apparatus. Our knowledge on intracellular GPCR function remains inc...
Autores principales: | Radoux-Mergault, Arthur, Oberhauser, Lucie, Aureli, Simone, Gervasio, Francesco Luigi, Stoeber, Miriam |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10115417/ https://www.ncbi.nlm.nih.gov/pubmed/37075112 http://dx.doi.org/10.1126/sciadv.adf6059 |
Ejemplares similares
-
Control of Gα(q) signaling dynamics and GPCR cross-talk by GRKs
por: Xiang, Guoqing, et al.
Publicado: (2022) -
Multiplexed selectivity screening of anti-GPCR antibodies
por: Dahl, Leo, et al.
Publicado: (2023) -
Atypical structural snapshots of human cytomegalovirus GPCR interactions with host G proteins
por: Tsutsumi, Naotaka, et al.
Publicado: (2022) -
Essential autoproteolysis of bacterial anti-σ factor RsgI for transmembrane signal transduction
por: Chen, Chao, et al.
Publicado: (2023) -
A molecular optomechanics approach reveals functional relevance of force transduction across talin and desmoplakin
por: Sadhanasatish, Tanmay, et al.
Publicado: (2023)