Oligomerization of the voltage-gated proton channel

Channels (Austin). 2010 Jul-Aug;4(4):260-5. doi: 10.4161/chan.4.4.12789. Epub 2010 Jul 24.

Abstract

The voltage-gated proton channel exists as a dimer, although each protomer has a separate conduction pathway, and when forced to exist as a monomer, most major functions are retained. However, the proton channel protomers appear to interact during gating. Proton channel dimerization is thought to result mainly from coiled-coil interaction of the intracellular C-termini. Several types of evidence are discussed that suggest that the dimer conformation may not be static, but is dynamic and can sample different orientations. Zn(2+) appears to link the protomers in an orientation from which the channel(s) cannot open. A tandem WT-WT dimer exhibits signs of cooperative gating, indicating that despite the abnormal linkage, the correct orientation for opening can occur. We propose that C-terminal interaction functions mainly to tether the protomers together. Comparison of the properties of monomeric and dimeric proton channels speaks against the hypothesis that enhanced gating reflects monomer-dimer interconversion.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Basophils / metabolism
  • Humans
  • Ion Channel Gating*
  • Ion Channels / chemistry
  • Ion Channels / genetics
  • Ion Channels / metabolism*
  • Kinetics
  • Membrane Potentials
  • Models, Molecular
  • Mutation
  • Protein Binding
  • Protein Conformation
  • Protein Interaction Domains and Motifs
  • Protein Multimerization
  • Protein Subunits
  • Protons
  • Structure-Activity Relationship
  • Zinc / metabolism

Substances

  • HVCN1 protein, human
  • Ion Channels
  • Protein Subunits
  • Protons
  • Zinc