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PMID: 2753152 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Purification and reconstitution of potassium channel proteins from squid axon membranes.

FEBS letters ·Vol. 250 ·No. 2 ·1989-07-03 ·Pages 570-4

Prestipino G, Valdivia HH, Liévano A, Darszon A, Ramírez AN, Possani LD

Abstract

Voltage-dependent K+ channels are responsible for repolarization of the cell membrane during the late phase of the action potential. Here we report the purification of proteins from squid axon membranes which bind the K+-channel blocker noxiustoxin (NTX), and their subsequent functional reconstitution in planar bilayers. The NTX-affinity purified proteins had Mr values of 60,000 +/- 6,000, 160,000 +/- 15,000 and 220,000 +/- 20,000. Their incorporation into bilayers resulted in single-channel currents with three conductances, the most frequent one of 11 pS in 300/100 mM KCl (cis/trans). The voltage dependence, reversal potential and bursting behavior suggest that these are the K+ channels involved in the squid axon action potential.

MeSH Terms
Animals Axons/metabolism Cell Membrane/metabolism Decapodiformes Electrophoresis, Polyacrylamide Gel Lipid Bilayers/metabolism Membrane Proteins/isolation & purification Potassium Channels/metabolism
Chemicals
Lipid Bilayers Membrane Proteins Potassium Channels
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Prestipino G
Istituto di Cibernetica e Biofisica, Genova, Italy.
Valdivia H H
Liévano A
Darszon A
Ramírez A N
Possani L D
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1989-07-03
Pages
570-4
Language
English
Region
England
NLM ID
0155157
Subset
IM
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