A cellular perspective of bias at G protein‐coupled receptors
Protein Science2020Vol. 29(6), pp. 1345–1354
Citations Over TimeTop 24% of 2020 papers
Abstract
G protein-coupled receptors (GPCRs) modulate cell function over short- and long-term timescales. GPCR signaling depends on biochemical parameters that define the what, when, and where of receptor function: what proteins mediate and regulate receptor signaling, where within the cell these interactions occur, and how long these interactions persist. These parameters can vary significantly depending on the activating ligand. Collectivity, differential agonist activity at a GPCR is called bias or functional selectivity. Here we review agonist bias at GPCRs with a focus on ligands that show dramatically different cellular responses from their unbiased counterparts.
Related Papers
- → GRK specificity and Gβγ dependency determines the potential of a GPCR for arrestin-biased agonism(2024)18 cited
- → Agonist‐selective signaling of G protein‐coupled receptor: Mechanisms and implications(2010)69 cited
- → Quantifying biased signaling in GPCRs using BRET-based biosensors(2015)41 cited
- → A cellular perspective of bias at G protein‐coupled receptors(2020)19 cited
- The complexity of G-protein coupled receptor-ligand interactions(2013)