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9JED

Cryo-EM structure of Histamine-bound Histamine receptor 4 H4R G protein complex

Summary for 9JED
Entry DOI10.2210/pdb9jed/pdb
EMDB information61413
DescriptorGuanine nucleotide-binding protein G(i) subunit alpha-1, 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, ... (8 entities in total)
Functional Keywordscomplex, membrane protein/immune system, membrane protein-immune system complex
Biological sourceHomo sapiens (human)
More
Total number of polymer chains5
Total formula weight154914.05
Authors
Jin, S.,Zhang, H.,Jiang, Y. (deposition date: 2024-09-03, release date: 2025-09-10)
Primary citationJin, S.S.,Zhang, H.,Yan, J.H.,Wu, C.R.,Cai, X.Q.,Wu, K.,Wang, M.W.,Xu, H.E.,Yang, D.H.,Jiang, Y.
Decoding ligand recognition and constitutive activation of histamine H3 and H4 receptors.
Acta Pharmacol.Sin., 2025
Cited by
PubMed Abstract: Histamine H3 receptor (H3R) and H4 receptor (H4R) are key members of the histamine receptor family, with H3R as a potential target for narcolepsy treatments and H4R as a candidate for next-generation antihistamines for inflammatory and allergic diseases. Although progress has been made in understanding the structure of histamine receptors, the detailed mechanisms of ligand recognition and receptor antagonism for H3R and H4R remain unclear. In this study, using cryo-electron microscopy, we present an inactive structure of H4R bound to a selective antagonist, adriforant, and two Gi-coupled structures of H3R and H4R in complex with histamine. Our structural and mutagenesis analyses provide insights into the selective binding of adriforant to H4R and the recognition of histamine across histamine receptors. Our findings also uncovered distinct antagonistic mechanisms for H3R and H4R and identified the role of aromatic amino acids on extracellular loop 2 in modulating the constitutive activity of H3R and H4R. These findings advance our knowledge of the functional modulation of histamine receptors, providing a foundation for the development of targeted therapeutics for neurological and immune-related disorders.
PubMed: 40877594
DOI: 10.1038/s41401-025-01633-4
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.58 Å)
Structure validation

244349

数据于2025-11-05公开中

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