Abstract
C-type inactivation of Shaker potassium channels involves entry into a state (or states) in which the inactivated channels appear nonconducting in physiological solutions. However, when Shaker channels, from which fast N-type inactivation has been removed by NH2-terminal deletions, are expressed in Xenopus oocytes and evaluated in inside-out patches, complete removal of K+ ions from the internal solution exposes conduction of Na+ and Li+ in C-type inactivated conformational states. The present paper uses this observation to investigate the properties of ion conduction through C-type inactivated channel states, and demonstrates that both activation and deactivation can occur in C-type states, although with slower than normal kinetics. Channels in the C-type states appear "inactivated" (i.e., nonconducting) in physiological solutions due to the summation of two separate effects: first, internal K+ ions prevent Na+ ions from permeating through the channel; second, C-type inactivation greatly reduces the permeability of K+ relative to the permeability of Na+, thus altering the ion selectivity of the channel.
MeSH Terms
Animals
Drosophila
Drosophila Proteins
Electric Conductivity
Female
Ions
Oocytes
Patch-Clamp Techniques
Permeability
Potassium/pharmacology
Potassium Channel Blockers
Potassium Channels/classification,metabolism
Shaker Superfamily of Potassium Channels
Sodium/physiology
Time Factors
Xenopus laevis
Chemicals
Drosophila Proteins
Ions
Potassium Channel Blockers
Potassium Channels
Sh protein, Drosophila
Shaker Superfamily of Potassium Channels
Sodium
Potassium
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Starkus J G
Research Unit Molecular and Cellular Biophysics, Max Planck Society, D-07747 Jena, Germany.
Kuschel L
Rayner M D
Heinemann S H
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