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PMID: 2010814 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Cloning and expression of an Aplysia K+ channel and comparison with native Aplysia K+ currents.

Pfaffinger PJ, Furukawa Y, Zhao B, Dugan D, Kandel ER

Abstract

We describe here the cloning of the Aplysia K+ channel AK01a.AK01a codes for a protein of 515 amino acids, shows considerable homology to other cloned potassium channels, and can be classified as a member of the ShakerK+ channel family. Expression of the AK01a channel in Xenopus oocytes produces a rapidly inactivating outward potassium current (IAK01a) resembling the A-type currents of Drosophila Shaker. Gating for this current is shifted to potentials considerably more positive than the traditional A-currents of Aplysia; we have, however, identified a novel transient potassium current (IAdepoI) in a subset of Aplysia neurons that has similar gating and pharmacological properties to IAK01a.

MeSH Terms
Amino Acid Sequence Animals Aplysia/metabolism Base Sequence Blotting, Northern Cloning, Molecular Electrochemistry Kinetics Molecular Sequence Data Oocytes/metabolism Potassium Channels/genetics,metabolism Sequence Homology, Nucleic Acid Tissue Distribution Xenopus/metabolism
Chemicals
Potassium Channels
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Pfaffinger P J
Howard Hughes Medical Institute, Department of Physiology and Biophysics, Columbia University, College of Physicians and Surgeons, New York, New York 10032.
Furukawa Y
Zhao B
Dugan D
Kandel E R
Article Info
Journal
The Journal of neuroscience : the official journal of the Society for Neuroscience
Abbr.
J Neurosci
ISSN
0270-6474
Published
1991-04-00
Pages
918-27
Language
English
Region
United States
NLM ID
8102140
PMCID
PMC6575383
Subset
IM
Databases
GENBANK
M95914, S63183, X53785, X53786, X59936, X59937, X63306, X63307, X63308, X63309
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