A versatile functional interaction between electrically silent KV subunits and KV7 potassium channels

Voltage-gated K + (K V ) channels govern K +  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 V channels (K V S), however, are unable to conduct currents on their own....

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Veröffentlicht in:Cellular and molecular life sciences : CMLS 2024-12, Vol.81 (1), p.301, Article 301
Hauptverfasser: Renigunta, Vijay, Xhaferri, Nermina, Shaikh, Imran Gousebasha, Schlegel, Jonathan, Bisen, Rajeshwari, Sanvido, Ilaria, Kalpachidou, Theodora, Kummer, Kai, Oliver, Dominik, Leitner, Michael G., Lindner, Moritz
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Sprache:eng
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Zusammenfassung:Voltage-gated K + (K V ) channels govern K +  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 V channels (K V S), however, are unable to conduct currents on their own. It has been assumed that these K V S must obligatorily assemble with subunits from the K V 2 family into heterotetrameric channels, thereby giving rise to currents distinct from those of homomeric K V 2 channels. Herein, we show that K V S subunits indeed also modulate the activity, biophysical properties and surface expression of recombinant K V 7 isoforms in a subunit-specific manner. Employing co-immunoprecipitation, and proximity labelling, we unveil the spatial coexistence of K V S and K V 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 V S and K V 7 interaction may occur. Our findings demonstrate that K V cross-family interaction is much more versatile than previously thought—possibly serving nature to shape potassium conductance to the needs of individual cell types.
ISSN:1420-682X
1420-9071
1420-9071
DOI:10.1007/s00018-024-05312-1