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PMID: 11212207 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Erg1, erg2 and erg3 K channel subunits are able to form heteromultimers.

Pflugers Archiv : European journal of physiology ·Vol. 441 ·No. 4 ·2001-01-00 ·Pages 450-5

Wimmers S, Wulfsen I, Bauer CK, Schwarz JR

Abstract

Clonal somato-mammotroph GH3/B6 cells and lactotroph MMQ cells express two (ergl, erg2) of the three cloned rat ether-à-go-go-related gene (erg) K channel subunits. To study whether the erg subunits form heteromultimers, dominant-negative mutants of erg and erg2 were constructed by point mutation (erg1G630S, erg2G480S). After co-expression of these mutants with the wild-type erg1, erg2, or erg3 in Chinese hamster ovary (CHO) cells no erg currents could be detected. In contrast, in co-expression experiments with members of the other ether-à-go-go (EAG) subfamilies (eagl, elkl) the mutant erg1G630S had no effect. These results strongly suggest that erg channel subunits are able to form heteromultimers within the erg channel subfamily. Suppression of the endogenous E-4031-sensitive currents in GH3/B6 and MMQ cells by erg1G630S confirms that they are mediated by erg channels despite the differences in gating kinetics in these cells. Reduction of the erg current in GH3/B6 cells by erg2G480S indicates that erg heteromultimers can also be formed in these cells.

MeSH Terms
Amino Acid Sequence Animals Base Sequence CHO Cells Cation Transport Proteins Cricetinae ERG1 Potassium Channel Electric Conductivity Ether-A-Go-Go Potassium Channels Macromolecular Substances Membrane Transport Proteins Mutagenesis, Site-Directed Potassium Channels/chemistry,genetics,physiology Potassium Channels, Voltage-Gated Rats Recombinant Proteins/chemistry Reverse Transcriptase Polymerase Chain Reaction Structure-Activity Relationship Transfection
Chemicals
Cation Transport Proteins ERG1 Potassium Channel Ether-A-Go-Go Potassium Channels KCNH2 protein, human KCNH6 protein, human KCNH7 protein, human Kcnh6 protein, rat Kcnh7 protein, rat Macromolecular Substances Membrane Transport Proteins Potassium Channels Potassium Channels, Voltage-Gated Recombinant Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Wimmers S
Abteilung für Angewandte Physiologie, Institut für Physiologie, Universitätsklinikum Hamburg-Eppendorf, Germany.
Wulfsen I
Bauer C K
Schwarz J R
Article Info
Journal
Pflugers Archiv : European journal of physiology
Abbr.
Pflugers Arch
ISSN
0031-6768
Published
2001-01-00
Pages
450-5
Language
English
Region
Germany
NLM ID
0154720
Subset
IM
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