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8ID6

Cryo-EM structure of the oleic acid bound GPR120-Gi complex

Summary for 8ID6
Entry DOI10.2210/pdb8id6/pdb
EMDB information35358
DescriptorFree fatty acid receptor 4, Guanine nucleotide-binding protein G(i) subunit alpha-1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ... (6 entities in total)
Functional Keywordsgpcr, gpr120, complex, fatty acid hormones, membrane protein
Biological sourceHomo sapiens (human)
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Total number of polymer chains5
Total formula weight156740.62
Authors
Mao, C.,Xiao, P.,Tao, X.,Qin, J.,He, Q.,Zhang, C.,Yu, X.,Zhang, Y.,Sun, J. (deposition date: 2023-02-12, release date: 2023-03-15, Last modification date: 2024-10-30)
Primary citationMao, C.,Xiao, P.,Tao, X.N.,Qin, J.,He, Q.T.,Zhang, C.,Guo, S.C.,Du, Y.Q.,Chen, L.N.,Shen, D.D.,Yang, Z.S.,Zhang, H.Q.,Huang, S.M.,He, Y.H.,Cheng, J.,Zhong, Y.N.,Shang, P.,Chen, J.,Zhang, D.L.,Wang, Q.L.,Liu, M.X.,Li, G.Y.,Guo, Y.,Xu, H.E.,Wang, C.,Zhang, C.,Feng, S.,Yu, X.,Zhang, Y.,Sun, J.P.
Unsaturated bond recognition leads to biased signal in a fatty acid receptor.
Science, 380:eadd6220-eadd6220, 2023
Cited by
PubMed Abstract: Individual free fatty acids (FAs) play important roles in metabolic homeostasis, many through engagement with more than 40G protein-coupled receptors. Searching for receptors to sense beneficial omega-3 FAs of fish oil enabled the identification of GPR120, which is involved in a spectrum of metabolic diseases. Here, we report six cryo-electron microscopy structures of GPR120 in complex with FA hormones or TUG891 and G or G trimers. Aromatic residues inside the GPR120 ligand pocket were responsible for recognizing different double-bond positions of these FAs and connect ligand recognition to distinct effector coupling. We also investigated synthetic ligand selectivity and the structural basis of missense single-nucleotide polymorphisms. We reveal how GPR120 differentiates rigid double bonds and flexible single bonds. The knowledge gleaned here may facilitate rational drug design targeting to GPR120.
PubMed: 36862765
DOI: 10.1126/science.add6220
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.8 Å)
Structure validation

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