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7T37

Activated state of 2-APB and CBD-bound wildtype rat TRPV2 in nanodiscs

Summary for 7T37
Entry DOI10.2210/pdb7t37/pdb
EMDB information25650 25651
DescriptorTransient receptor potential cation channel subfamily V member 2, cannabidiol, 2-aminoethyl diphenylborinate (3 entities in total)
Functional Keywordstrp channel, ion channel, trpv, transport protein
Biological sourceRattus norvegicus (Norway rat)
Total number of polymer chains4
Total formula weight349353.79
Authors
Pumroy, R.A.,Protopopova, A.D.,Gallo, P.N.,Moiseenkova-Bell, V.Y. (deposition date: 2021-12-07, release date: 2022-05-04, Last modification date: 2024-02-28)
Primary citationPumroy, 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: 35484159
DOI: 10.1038/s41467-022-30083-3
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.7 Å)
Structure validation

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