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PMID: 7890032 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Molecular cloning and functional expression of a novel potassium channel beta-subunit from human atrium.

FEBS letters ·Vol. 361 ·No. 1 ·1995-03-13 ·Pages 13-6

Majumder K, De Biasi M, Wang Z, Wible BA

Abstract

We report the cloning and functional expression of a novel K+ channel beta-subunit from human atrium, hKv beta 3. hKv beta 3 is highly homologous to the two beta-subunits cloned from rat brain, Kv beta 1 and Kv beta 2, but has an essentially unique stretch of 79 N-terminal residues. Upon expression in Xenopus oocytes, hKv beta 3 accelerates the inactivation of co-injected hKv1.4 currents and induces fast inactivation of non-inactivating co-injected hKv1.5 currents. By contrast, hKv beta 3 had no effect on hKv1.1, hKv1.2, or hKv2.1 currents. Thus, hKv beta 3 represents a third type of K+ channel beta-subunit which modulates the kinetics of a unique subset of channels in the Kv1 subfamily.

MeSH Terms
Amino Acid Sequence Animals Atrial Function Base Sequence Cloning, Molecular Humans Ion Channel Gating/genetics Membrane Potentials Molecular Sequence Data Oocytes Potassium Channels/biosynthesis,genetics,physiology RNA, Messenger/genetics Rats Sequence Analysis, DNA Sequence Homology, Amino Acid Xenopus
Chemicals
Potassium Channels RNA, Messenger
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Majumder K
Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX 77030.
De Biasi M
Wang Z
Wible B A
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1995-03-13
Pages
13-6
Language
English
Region
England
NLM ID
0155157
Subset
IM
Grants
NHLBI NIH HHS · HL36930 · United States
NHLBI NIH HHS · HL37044 · United States
Databases
GENBANK
U16953
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