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A versatile functional interaction between electrically silent K V subunits and K V 7 potassium channels.

Authors :
Renigunta V
Xhaferri N
Shaikh IG
Schlegel J
Bisen R
Sanvido I
Kalpachidou T
Kummer K
Oliver D
Leitner MG
Lindner M
Source :
Cellular and molecular life sciences : CMLS [Cell Mol Life Sci] 2024 Jul 14; Vol. 81 (1), pp. 301. Date of Electronic Publication: 2024 Jul 14.
Publication Year :
2024

Abstract

Voltage-gated K <superscript>+</superscript> (K <subscript>V</subscript> ) channels govern K <superscript>+</superscript>  ion flux across cell membranes in response to changes in membrane potential. They are formed by the assembly of four subunits, typically from the same family. Electrically silent K <subscript>V</subscript> channels (K <subscript>V</subscript> S), however, are unable to conduct currents on their own. It has been assumed that these K <subscript>V</subscript> S must obligatorily assemble with subunits from the K <subscript>V</subscript> 2 family into heterotetrameric channels, thereby giving rise to currents distinct from those of homomeric K <subscript>V</subscript> 2 channels. Herein, we show that K <subscript>V</subscript> S subunits indeed also modulate the activity, biophysical properties and surface expression of recombinant K <subscript>V</subscript> 7 isoforms in a subunit-specific manner. Employing co-immunoprecipitation, and proximity labelling, we unveil the spatial coexistence of K <subscript>V</subscript> S and K <subscript>V</subscript> 7 within a single protein complex. Electrophysiological experiments further indicate functional interaction and probably heterotetramer formation. Finally, single-cell transcriptomic analyses identify native cell types in which this K <subscript>V</subscript> S and K <subscript>V</subscript> 7 interaction may occur. Our findings demonstrate that K <subscript>V</subscript> cross-family interaction is much more versatile than previously thought-possibly serving nature to shape potassium conductance to the needs of individual cell types.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1420-9071
Volume :
81
Issue :
1
Database :
MEDLINE
Journal :
Cellular and molecular life sciences : CMLS
Publication Type :
Academic Journal
Accession number :
39003683
Full Text :
https://doi.org/10.1007/s00018-024-05312-1