ENaC structure and function in the wake of a resolved structure of a family member

Am J Physiol Renal Physiol. 2011 Oct;301(4):F684-96. doi: 10.1152/ajprenal.00259.2011. Epub 2011 Jul 13.

Abstract

Our understanding of epithelial Na(+) channel (ENaC) structure and function has been profoundly impacted by the resolved structure of the homologous acid-sensing ion channel 1 (ASIC1). The structure of the extracellular and pore regions provide insight into channel assembly, processing, and the ability of these channels to sense the external environment. The absence of intracellular structures precludes insight into important interactions with intracellular factors that regulate trafficking and function. The primary sequences of ASIC1 and ENaC subunits are well conserved within the regions that are within or in close proximity to the plasma membrane, but poorly conserved in peripheral domains that may functionally differentiate family members. This review examines functional data, including ion selectivity, gating, and amiloride block, in light of the resolved ASIC1 structure.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Acid Sensing Ion Channels
  • Amiloride / pharmacology
  • Amino Acid Sequence
  • Animals
  • Chlorides / physiology
  • Conserved Sequence
  • Epithelial Sodium Channels / drug effects
  • Epithelial Sodium Channels / physiology*
  • Humans
  • Ion Channel Gating / drug effects
  • Ion Channel Gating / physiology
  • Mice
  • Molecular Sequence Data
  • Nerve Tissue Proteins / drug effects
  • Nerve Tissue Proteins / physiology
  • Rats
  • Sequence Homology, Amino Acid
  • Sodium Channel Blockers / pharmacology
  • Sodium Channels / drug effects
  • Sodium Channels / physiology
  • Structure-Activity Relationship

Substances

  • ASIC1 protein, human
  • ASIC1 protein, mouse
  • Acid Sensing Ion Channels
  • Asic1 protein, rat
  • Chlorides
  • Epithelial Sodium Channels
  • Nerve Tissue Proteins
  • Sodium Channel Blockers
  • Sodium Channels
  • Amiloride