It takes two to Tango: Two gates orchestrate the opening of human TRPM2

Cell Calcium. 2022 Jan:101:102523. doi: 10.1016/j.ceca.2021.102523. Epub 2021 Dec 23.

Abstract

TRPM2 is a calcium permeable non-selective cation channel involved in many important physiological processes and has divergent gating mechanisms across species. Structural studies have revealed that TRPM2 is gated by adenosine 5'-diphosphoribose that binds to the cytosolic domains of TRPM2 and calcium ions that are coordinated by residues in the transmembrane domain. However, the selectivity filter of human TRPM2 remains elusive due to the poor resolution in this region. In a recent manuscript published in Cell Reports, Yu et al. present unexpected dual roles of the selectivity filter in human TRPM2 by determining a high-resolution structure of human TRPM2 in lipid nanodiscs. This study provides unprecedented insights into the gating mechanism of human TRPM2.

MeSH terms

  • Adenosine Diphosphate Ribose
  • Calcium / metabolism
  • Humans
  • Ion Channel Gating
  • Protein Domains
  • TRPM Cation Channels* / metabolism

Substances

  • TRPM Cation Channels
  • TRPM2 protein, human
  • Adenosine Diphosphate Ribose
  • Calcium