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Publication Abstract from PubMed

The adenosine A(3) receptor (A(3)AR), a key member of the G protein-coupled receptor family, is a promising therapeutic target for inflammatory and cancerous conditions. The selective A(3)AR agonists, CF101 and CF102, are clinically significant, yet their recognition mechanisms remained elusive. Here we report the cryogenic electron microscopy structures of the full-length human A(3)AR bound to CF101 and CF102 with heterotrimeric G(i) protein in complex at 3.3-3.2 A resolution. These agonists reside in the orthosteric pocket, forming conserved interactions via their adenine moieties, while their 3-iodobenzyl groups exhibit distinct orientations. Functional assays reveal the critical role of extracellular loop 3 in A(3)AR's ligand selectivity and receptor activation. Key mutations, including His(3.37), Ser(5.42), and Ser(6.52), in a unique sub-pocket of A(3)AR, significantly impact receptor activation. Comparative analysis with the inactive A(2A)AR structure highlights a conserved receptor activation mechanism. Our findings provide comprehensive insights into the molecular recognition and signaling of A(3)AR, paving the way for designing subtype-selective adenosine receptor ligands.

Cryo-EM structures of adenosine receptor A(3)AR bound to selective agonists.,Cai H, Guo S, Xu Y, Sun J, Li J, Xia Z, Jiang Y, Xie X, Xu HE Nat Commun. 2024 Apr 16;15(1):3252. doi: 10.1038/s41467-024-47207-6. PMID:38627384^[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.