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8ZW0

Cryo-EM strcuture of Prostaglandin D2 Receptor DP1 activated by PGD2

Summary for 8ZW0
Entry DOI10.2210/pdb8zw0/pdb
EMDB information60514
DescriptorGuanine nucleotide-binding protein G(s) subunit alpha isoforms short, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Soluble cytochrome b562,Prostaglandin D2 receptor, ... (7 entities in total)
Functional Keywordsprostaglandin, dp1, pgd2, membrane protein
Biological sourceHomo sapiens (human)
More
Total number of polymer chains5
Total formula weight161583.79
Authors
Xu, J.,Xu, Y.,Wu, C.,Xu, H.E. (deposition date: 2024-06-12, release date: 2025-05-28, Last modification date: 2025-06-25)
Primary citationXu, J.,Wu, Y.,Xu, Y.,Li, Y.,He, X.,Zhang, H.,Wang, J.J.,Hou, J.,Li, J.,Hu, W.,Wu, K.,Yuan, Q.,Wu, C.,Xu, H.E.
Molecular basis for ligand recognition and receptor activation of the prostaglandin D2 receptor DP1.
Proc.Natl.Acad.Sci.USA, 122:e2501902122-e2501902122, 2025
Cited by
PubMed Abstract: The prostaglandin D2 receptor 1 (DP1), a rhodopsin-like Class A GPCR, orchestrates critical physiological and pathological processes, ranging from sleep regulation to inflammatory responses and cardiovascular function. Despite its therapeutic significance, structural insights into DP1 activation mechanisms have remained elusive. Here, using cryoelectron microscopy (cryo-EM), we determined high-resolution structures of human DP1 in both inactive and active states, with the latter captured in complex with its endogenous agonist PGD2 or the synthetic agonist BW245C, bound to the stimulatory G protein, Gs. Our structures, coupled with functional and mutagenesis studies, unveiled unique structural features of DP1, including an alternative activation mechanism, ligand-selectivity determinants, and G protein coupling characteristics. These molecular insights provide a rational framework for designing selective DP1-targeted therapeutics, both agonists and antagonists, with enhanced specificity and reduced off-target effects, opening broad avenues for treating DP1-associated disorders.
PubMed: 40440061
DOI: 10.1073/pnas.2501902122
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.72 Å)
Structure validation

238895

数据于2025-07-16公开中

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