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PMID: 8562074 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Molecular basis of charge movement in voltage-gated sodium channels.

Neuron ·Vol. 16 ·No. 1 ·1996-01-00 ·Pages 113-22

Yang N, George AL, Horn R

Abstract

Voltage-dependent movement of a sodium channel S4 segment was examined by cysteine scanning mutagenesis and testing accessibility of the residues to hydrophilic cysteine-modifying reagents. These experiments indicate that 2 charged S4 residues move completely from an internally accessible to an externally accessible location in response to depolarization by passage through a short "channel" in the protein. The energetic problems of S4 movement have thus been solved in the same way that may ion channels achieve highly selective and rapid ion permeation through an open pore, by restricting the contact region between the permion and its channel.

MeSH Terms
Amino Acid Sequence Base Sequence Cell Line Chemical Phenomena Chemistry, Physical Cysteine/chemistry Humans Ion Channel Gating/drug effects,physiology Membrane Potentials/drug effects Models, Molecular Molecular Sequence Data Muscle, Skeletal/chemistry Mutagenesis, Site-Directed Protein Conformation Recombinant Fusion Proteins/chemistry Sodium/physiology Sodium Channels/chemistry,drug effects,genetics,physiology Sulfhydryl Reagents/pharmacology Transfection
Chemicals
Recombinant Fusion Proteins Sodium Channels Sulfhydryl Reagents Sodium Cysteine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Yang N
Department of Physiology, Jefferson Medical College, Philadelphia, Pennsylvania 19107, USA.
George A L
Horn R
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
1996-01-00
Pages
113-22
Language
English
Region
United States
NLM ID
8809320
Subset
IM
Grants
NIAMS NIH HHS · AR41691 · United States
NINDS NIH HHS · NS32387 · United States
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