7N0M
Inactivated state of 2-APB-bound wildtype rat TRPV2 in nanodiscs
Summary for 7N0M
| Entry DOI | 10.2210/pdb7n0m/pdb |
| EMDB information | 24109 24110 |
| Descriptor | Transient receptor potential cation channel subfamily V member 2, 2-aminoethyl diphenylborinate (2 entities in total) |
| Functional Keywords | trp channel, ion channel, trpv, transport protein |
| Biological source | Rattus norvegicus (Rat) |
| Total number of polymer chains | 4 |
| Total formula weight | 348095.94 |
| Authors | Pumroy, R.A.,Protopopova, A.D.,Gallo, P.N.,Moiseenkova-Bell, V.Y. (deposition date: 2021-05-25, release date: 2022-05-04, Last modification date: 2024-05-29) |
| Primary citation | Pumroy, R.A.,Protopopova, A.D.,Fricke, T.C.,Lange, I.U.,Haug, F.M.,Nguyen, P.T.,Gallo, P.N.,Sousa, B.B.,Bernardes, G.J.L.,Yarov-Yarovoy, V.,Leffler, A.,Moiseenkova-Bell, V.Y. Structural insights into TRPV2 activation by small molecules. Nat Commun, 13:2334-2334, 2022 Cited by PubMed Abstract: Transient receptor potential vanilloid 2 (TRPV2) is involved in many critical physiological and pathophysiological processes, making it a promising drug target. Here we present cryo-electron microscopy (cryo-EM) structures of rat TRPV2 in lipid nanodiscs activated by 2-aminoethoxydiphenyl borate (2-APB) and propose a TRPV2-specific 2-ABP binding site at the interface of S5 of one monomer and the S4-S5 linker of the adjacent monomer. In silico docking and electrophysiological studies confirm the key role of His521 and Arg539 in 2-APB activation of TRPV2. Additionally, electrophysiological experiments show that the combination of 2-APB and cannabidiol has a synergetic effect on TRPV2 activation, and cryo-EM structures demonstrate that both drugs were able to bind simultaneously. Together, our cryo-EM structures represent multiple functional states of the channel, providing a native picture of TRPV2 activation by small molecules and a structural framework for the development of TRPV2-specific activators. PubMed: 35484159DOI: 10.1038/s41467-022-30083-3 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.5 Å) |
Structure validation
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