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8FFQ

Wildtype rabbit TRPV5 into nanodiscs in the presence of PI(4,5)P2 and ruthenium red

Summary for 8FFQ
Entry DOI10.2210/pdb8ffq/pdb
EMDB information29051
DescriptorTransient receptor potential cation channel subfamily V member 5, ERGOSTEROL, ruthenium(6+) azanide pentaamino(oxido)ruthenium (1/4/2), ... (4 entities in total)
Functional Keywordstrpv5, trp channel, ruthenium red, pi(4, 5)p2, membrane protein
Biological sourceOryctolagus cuniculus (rabbit)
Total number of polymer chains4
Total formula weight341903.29
Authors
De Jesus-Perez, J.J.,Fluck, E.C.,Pumroy, R.A.,Protopopova, A.D.,Rocereta, J.A.,Moiseenkova-Bell, V.Y. (deposition date: 2022-12-09, release date: 2024-02-07, Last modification date: 2024-02-21)
Primary citationPumroy, R.A.,De Jesus-Perez, J.J.,Protopopova, A.D.,Rocereta, J.A.,Fluck, E.C.,Fricke, T.,Lee, B.H.,Rohacs, T.,Leffler, A.,Moiseenkova-Bell, V.
Molecular details of ruthenium red pore block in TRPV channels.
Embo Rep., 25:506-523, 2024
Cited by
PubMed Abstract: Transient receptor potential vanilloid (TRPV) channels play a critical role in calcium homeostasis, pain sensation, immunological response, and cancer progression. TRPV channels are blocked by ruthenium red (RR), a universal pore blocker for a wide array of cation channels. Here we use cryo-electron microscopy to reveal the molecular details of RR block in TRPV2 and TRPV5, members of the two TRPV subfamilies. In TRPV2 activated by 2-aminoethoxydiphenyl borate, RR is tightly coordinated in the open selectivity filter, blocking ion flow and preventing channel inactivation. In TRPV5 activated by phosphatidylinositol 4,5-bisphosphate, RR blocks the selectivity filter and closes the lower gate through an interaction with polar residues in the pore vestibule. Together, our results provide a detailed understanding of TRPV subfamily pore block, the dynamic nature of the selectivity filter and allosteric communication between the selectivity filter and lower gate.
PubMed: 38225355
DOI: 10.1038/s44319-023-00050-0
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.65 Å)
Structure validation

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