Functional reconstitution of purified human Hv1 H+ channels

J Mol Biol. 2009 Apr 17;387(5):1055-60. doi: 10.1016/j.jmb.2009.02.034. Epub 2009 Feb 21.

Abstract

Voltage-dependent H(+) (Hv) channels mediate proton conduction into and out of cells under the control of membrane voltage. Hv channels are unusual compared to voltage-dependent K(+), Na(+), and Ca(2+) channels in that Hv channel genes encode a voltage sensor domain (VSD) without a pore domain. The H(+) currents observed when Hv channels are expressed heterologously suggest that the VSD itself provides the pathway for proton conduction. In order to exclude the possibility that the Hv channel VSD assembles with an as yet unknown protein in the cell membrane as a requirement for H(+) conduction, we have purified Hv channels to homogeneity and reconstituted them into synthetic lipid liposomes. The Hv channel VSD by itself supports H(+) flux.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Electrochemistry
  • Fluorescence
  • Humans
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Ion Channels / genetics
  • Ion Channels / isolation & purification
  • Ion Channels / metabolism*
  • Liposomes
  • Protons
  • Recombinant Proteins / genetics
  • Recombinant Proteins / isolation & purification
  • Recombinant Proteins / metabolism

Substances

  • HVCN1 protein, human
  • Ion Channels
  • Liposomes
  • Protons
  • Recombinant Proteins