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PMID: 7568278 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Subunit-dependent assembly of inward-rectifier K+ channels.

Proceedings. Biological sciences ·Vol. 261 ·No. 1361 ·1995-08-22 ·Pages 251-61

Glowatzki E, Fakler G, Brändle U, Rexhausen U, Zenner HP, Ruppersberg JP, Fakler B

Abstract

Inward-rectifier, G-protein-regulated and ATP-dependent K+ channels form a novel gene family of related proteins which share two transmembrane segments as a common structural feature. These K+ channels are only distantly related to the voltage-gated Shaker-type K+ channels comprising six transmembrane segments. Although the quaternary structure of voltage-gated K+ channels has been extensively studied in the past, little is known about subunit assembly of inward-rectifier K+ channels. Differential sensitivity of inward-rectifier K+ channels to voltage-dependent pore block by spermine was used to analyse subunit assembly. It is shown that inward-rectifier K+ channel proteins are composed of four subunits whose assembly obeys the rules of a binomial distribution. 'Strong' and 'mild' inward-rectifier K+ channel subunits (BIR10 and ROMK1) which are co-expressed in individual auditory hair cells form hetero-tetramers. Distribution of these hetero-tetramers, however, is not binomial. Hetero- and homo-oligomeric channels form with similar probabilities resulting in independent channel populations with distinct functional properties.

MeSH Terms
Adenosine Triphosphate/metabolism Animals Base Sequence Cloning, Molecular DNA Primers/genetics Female GTP-Binding Proteins/metabolism Gene Expression Hair Cells, Auditory, Outer/metabolism Kinetics Molecular Sequence Data Oocytes/metabolism Polymerase Chain Reaction Potassium Channels/chemistry,genetics,metabolism Protein Conformation Rats Recombinant Proteins/chemistry,genetics,metabolism Xenopus
Chemicals
DNA Primers Potassium Channels Recombinant Proteins Adenosine Triphosphate GTP-Binding Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Glowatzki E
Department of Sensory Biophysics, ENT-Hospital of the University of Tübingen, Germany.
Fakler G
Brändle U
Rexhausen U
Zenner H P
Ruppersberg J P
Fakler B
Article Info
Journal
Proceedings. Biological sciences
Abbr.
Proc Biol Sci
ISSN
0962-8452
Published
1995-08-22
Pages
251-61
Language
English
Region
England
NLM ID
101245157
Subset
IM
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