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Functional Reconstitution of Purified Human Hv1 H Channels
Authors:Seok-Yong Lee  Roderick MacKinnon
Institution:Howard Hughes Medical Institute, Laboratory of Molecular Neurobiology and Biophysics, Rockefeller University, 1230 York Avenue, New York, NY 10065, USA
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 Ca2+ 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.
Keywords:Hv  voltage-dependent H+  VSD  voltage sensor domain  ACMA  9-amino-6-chloro-2-methoxyacridine  CCCP  carbonyl cyanide m-chlorophenyl hydrazone  DDM  d-maltopyranoside" target="_blank">n-dodecyl-β-d-maltopyranoside  DM  d-maltopyranoside" target="_blank">n-decyl-β-d-maltopyranoside  EDTA  ethylenediaminetetraacetic acid  EGTA  ethylene glycol bis(β-aminoethyl ether) N  N&prime  -tetraacetic acid
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