Ion Selectivity in the ENaC/DEG Family: A Systematic Review with Supporting Analysis

Int J Mol Sci. 2021 Oct 12;22(20):10998. doi: 10.3390/ijms222010998.

Abstract

The Epithelial Sodium Channel/Degenerin (ENaC/DEG) family is a superfamily of sodium-selective channels that play diverse and important physiological roles in a wide variety of animal species. Despite their differences, they share a high homology in the pore region in which the ion discrimination takes place. Although ion selectivity has been studied for decades, the mechanisms underlying this selectivity for trimeric channels, and particularly for the ENaC/DEG family, are still poorly understood. This systematic review follows PRISMA guidelines and aims to determine the main components that govern ion selectivity in the ENaC/DEG family. In total, 27 papers from three online databases were included according to specific exclusion and inclusion criteria. It was found that the G/SxS selectivity filter (glycine/serine, non-conserved residue, serine) and other well conserved residues play a crucial role in ion selectivity. Depending on the ion type, residues with different properties are involved in ion permeability. For lithium against sodium, aromatic residues upstream of the selectivity filter seem to be important, whereas for sodium against potassium, negatively charged residues downstream of the selectivity filter seem to be important. This review provides new perspectives for further studies to unravel the mechanisms of ion selectivity.

Keywords: FMRF-amide-gated sodium channel; acid-sensing ion channel; degenerin; epithelial sodium channel; ion selectivity; lithium; potassium; sodium.

Publication types

  • Systematic Review

MeSH terms

  • Amiloride / chemistry
  • Amiloride / metabolism
  • Animals
  • Epithelial Sodium Channels / chemistry
  • Epithelial Sodium Channels / genetics
  • Epithelial Sodium Channels / metabolism*
  • Humans
  • Ion Transport
  • Lithium / metabolism
  • Molecular Dynamics Simulation
  • Mutagenesis, Site-Directed
  • Protein Structure, Quaternary
  • Sodium / metabolism

Substances

  • Epithelial Sodium Channels
  • Amiloride
  • Lithium
  • Sodium