Molecular details of ruthenium red pore block in TRPV channels

EMBO Rep. 2024 Feb;25(2):506-523. doi: 10.1038/s44319-023-00050-0. Epub 2024 Jan 15.

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.

Keywords: Channel Activation and Blocking; Cryo-Electron Microscopy; Pore Blocker; Ruthenium Red; TRPV Channels.

MeSH terms

  • Antineoplastic Agents*
  • Calcium / metabolism
  • Cryoelectron Microscopy
  • Ruthenium Red / pharmacology
  • TRPV Cation Channels / genetics
  • Transient Receptor Potential Channels*

Substances

  • Transient Receptor Potential Channels
  • TRPV Cation Channels
  • Ruthenium Red
  • Antineoplastic Agents
  • Calcium