5YVE

Crystal structure of human P2X3 receptor in complex with the AF-219 negative allosteric modulator

Summary for 5YVE

• Entry DOI: 10.2210/pdb5yve/pdb
• Descriptor: P2X purinoceptor 3, MAGNESIUM ION, SODIUM ION, ... (5 entities in total)
• Functional Keywords: ion channels, atp, transport protein
• Biological source: Homo sapiens (Human)
• Cellular location: Membrane; Multi-pass membrane protein: P56373
• Total number of polymer chains: 1
• Total formula weight: 41737.19

Authors

Wang, Y.,Hattori, M. (deposition date: 2017-11-25, release date: 2018-04-04, Last modification date: 2024-10-16)

Primary citation

Wang, J.,Wang, Y.,Cui, W.W.,Huang, Y.,Yang, Y.,Liu, Y.,Zhao, W.S.,Cheng, X.Y.,Sun, W.S.,Cao, P.,Zhu, M.X.,Wang, R.,Hattori, M.,Yu, Y.
Druggable negative allosteric site of P2X3 receptors.
Proc. Natl. Acad. Sci. U.S.A., 115:4939-4944, 2018

PubMed Abstract: Allosteric modulation provides exciting opportunities for drug discovery of enzymes, ion channels, and G protein-coupled receptors. As cation channels gated by extracellular ATP, P2X receptors have attracted wide attention as new drug targets. Although small molecules targeting P2X receptors have entered into clinical trials for rheumatoid arthritis, cough, and pain, negative allosteric modulation of these receptors remains largely unexplored. Here, combining X-ray crystallography, computational modeling, and functional studies of channel mutants, we identified a negative allosteric site on P2X3 receptors, fostered by the left flipper (LF), lower body (LB), and dorsal fin (DF) domains. Using two structurally analogous subtype-specific allosteric inhibitors of P2X3, AF-353 and AF-219, the latter being a drug candidate under phase II clinical trials for refractory chronic cough and idiopathic pulmonary fibrosis, we defined the molecular interactions between the drugs and receptors and the mechanism by which allosteric changes in the LF, DF, and LB domains modulate ATP activation of P2X3. Our detailed characterization of this druggable allosteric site should inspire new strategies to develop P2X3-specific allosteric modulators for clinical use.

PubMed: 29674445
DOI: 10.1073/pnas.1800907115

Experimental method

X-RAY DIFFRACTION (3.4 Å)