Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

9JCP

Cryo-EM structure of the proton-sensing GPCR (GPR4)-Gq protein complex at pH 7.4

This is a non-PDB format compatible entry.
Summary for 9JCP
Entry DOI10.2210/pdb9jcp/pdb
EMDB information61371
DescriptorGuanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, Nanobody 35, ... (8 entities in total)
Functional Keywordscryo-em, gpcr, proton-sensing, gpr4, ph 7.4, gq, complex, signaling protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains5
Total formula weight161868.92
Authors
Xu, H.E.,You, C.,Jiang, Y. (deposition date: 2024-08-30, release date: 2025-07-09)
Primary citationYou, C.,Guo, S.,Zhang, T.,He, X.,Gao, T.,Xin, W.,Zhu, Z.,Lu, Y.,Xu, Y.,Li, Z.,Zhang, Y.,Cheng, X.,Jiang, Y.,Xie, X.,Xu, H.E.
Molecular mechanism of pH sensing and activation in GPR4 reveals proton-mediated GPCR signaling.
Cell Discov, 11:59-59, 2025
Cited by
PubMed Abstract: Maintaining pH homeostasis is critical for cellular function across all living organisms. Proton-sensing G protein-coupled receptors (GPCRs), particularly GPR4, play a pivotal role in cellular responses to pH changes. Yet, the molecular mechanisms underlying their proton sensing and activation remain incompletely understood. Here we present high-resolution cryo-electron microscopy structures of GPR4 in complex with G proteins under physiological and acidic pH conditions. Our structures reveal an intricate proton-sensing mechanism driven by a sophisticated histidine network in the receptor's extracellular domain. Upon protonation of key histidines under acidic conditions, a remarkable conformational cascade is initiated, propagating from the extracellular region to the intracellular G protein-coupling interface. This dynamic process involves precise transmembrane helix rearrangements and conformational shifts of conserved motifs, mediated by strategically positioned water molecules. Notably, we discovered a bound bioactive lipid, lysophosphatidylcholine, which has positive allosteric effects on GPR4 activation. These findings provide a comprehensive framework for understanding proton sensing in GPCRs and the interplay between pH sensing and lipid regulation, offering insights into cellular pH homeostasis and potential therapies for pH-related disorders.
PubMed: 40555728
DOI: 10.1038/s41421-025-00807-y
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.55 Å)
Structure validation

243083

数据于2025-10-15公开中

PDB statisticsPDBj update infoContact PDBjnumon