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PMID: 9746524 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Loss of shaker K channel conductance in 0 K+ solutions: role of the voltage sensor.

Biophysical journal ·Vol. 75 ·No. 4 ·1998-10-00 ·Pages 1828-35

Melishchuk A, Loboda A, Armstrong CM

Abstract

In potassium-free solutions some types of K channels enter a long-lasting nonconducting or "defunct" state. It is known that Shaker K channels must open in K+-free solutions to become defunct. Gating current studies presented here indicate an abnormal conformation in the defunct state that restricts S4 movement and alters its kinetics. Thus an abnormality initiated in the P region spreads to the gating apparatus. We find that channels most readily become defunct on repolarization to an intermediate voltage, thus prolonging occupancy of one of the several intermediate closed states. The state dependence of becoming defunct was further dissected by using the gating mutant L382A. Simply closing this channel at 0 mV (reversing the last activation step) does not make the mutant channel defunct. Instead, it is necessary to move further left (more fully closed) in the activation sequence. This was confirmed with ShIR experiments showing that channels become defunct only if there is inward gating charge movement. Rapid transit through the intermediate states, achieved at very negative voltage, is relatively ineffective at making channels defunct. Several mutations that removed C-type inactivation also made the channels resistant to becoming defunct. Our results show that normal gating current cannot be stably recorded in the absence of K+.

MeSH Terms
Amino Acid Substitution Cell Line Cloning, Molecular Electric Conductivity Humans Ion Channel Gating/physiology Kinetics Models, Biological Models, Molecular Mutagenesis, Site-Directed Patch-Clamp Techniques Polymerase Chain Reaction Potassium/physiology Potassium Channels/chemistry,physiology Protein Conformation Recombinant Proteins/chemistry,metabolism Shaker Superfamily of Potassium Channels Time Factors Transfection
Chemicals
Potassium Channels Recombinant Proteins Shaker Superfamily of Potassium Channels Potassium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Melishchuk A
Department of Physiology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA. melischu@mail.med.upenn.edu
Loboda A
Armstrong C M
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Article Info
Journal
Biophysical journal
Abbr.
Biophys J
ISSN
0006-3495
Published
1998-10-00
Pages
1828-35
Language
English
Region
United States
NLM ID
0370626
PMCID
PMC1299854
Subset
IM
Grants
NINDS NIH HHS · NS12547 · United States
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