Structural Biology of G Protein-coupled Receptor Signaling Complexes
Overview
Authors
Affiliations
G protein-coupled receptors (GPCRs) constitute the largest family of cell surface receptors that mediate numerous cell signaling pathways, and are targets of more than one-third of clinical drugs. Thanks to the advancement of novel structural biology technologies, high-resolution structures of GPCRs in complex with their signaling transducers, including G-protein and arrestin, have been determined. These 3D complex structures have significantly improved our understanding of the molecular mechanism of GPCR signaling and provided a structural basis for signaling-biased drug discovery targeting GPCRs. Here we summarize structural studies of GPCR signaling complexes with G protein and arrestin using rhodopsin as a model system, and highlight the key features of GPCR conformational states in biased signaling including the sequence motifs of receptor TM6 that determine selective coupling of G proteins, and the phosphorylation codes of GPCRs for arrestin recruitment. We envision the future of GPCR structural biology not only to solve more high-resolution complex structures but also to show stepwise GPCR signaling complex assembly and disassembly and dynamic process of GPCR signal transduction.
AI-driven antibody design with generative diffusion models: current insights and future directions.
He X, Li J, Xu J, Shan H, Shen S, Gao S Acta Pharmacol Sin. 2024; 46(3):565-574.
PMID: 39349764 PMC: 11845702. DOI: 10.1038/s41401-024-01380-y.
Receptor Pharmacogenomics: Deciphering Genetic Influence on Drug Response.
Anghel S, Dinu-Pirvu C, Costache M, Voiculescu A, Ghica M, Anuta V Int J Mol Sci. 2024; 25(17).
PMID: 39273318 PMC: 11395000. DOI: 10.3390/ijms25179371.
Molecular mechanism of β-arrestin-2 pre-activation by phosphatidylinositol 4,5-bisphosphate.
Kim K, Chung K EMBO Rep. 2024; 25(10):4190-4205.
PMID: 39242774 PMC: 11467438. DOI: 10.1038/s44319-024-00239-x.
Lander A, Kong Y, Jin Y, Wu C, Luk L ACS Bio Med Chem Au. 2024; 4(1):68-76.
PMID: 38404743 PMC: 10885103. DOI: 10.1021/acsbiomedchemau.3c00060.
Yuan S, Xia L, Wang C, Wu F, Zhang B, Pan C ACS Cent Sci. 2023; 9(5):992-1007.
PMID: 37252352 PMC: 10214531. DOI: 10.1021/acscentsci.3c00063.