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 DOI | 10.2210/pdb9jcp/pdb |
EMDB information | 61371 |
Descriptor | Guanine 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 Keywords | cryo-em, gpcr, proton-sensing, gpr4, ph 7.4, gq, complex, signaling protein |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 5 |
Total formula weight | 161868.92 |
Authors | |
Primary citation | You, 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: 40555728DOI: 10.1038/s41421-025-00807-y PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (2.55 Å) |
Structure validation
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