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XB-ART-11260
J Biol Chem 2000 Jun 02;27522:16969-78. doi: 10.1074/jbc.M001948200.
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Proton block and voltage gating are potassium-dependent in the cardiac leak channel Kcnk3.

Lopes CM , Gallagher PG , Buck ME , Butler MH , Goldstein SA .


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Potassium leak conductances were recently revealed to exist as independent molecular entities. Here, the genomic structure, cardiac localization, and biophysical properties of a murine example are considered. Kcnk3 subunits have two pore-forming P domains and unique functional attributes. At steady state, Kcnk3 channels behave like open, potassium-selective, transmembrane holes that are inhibited by physiological levels of proton. With voltage steps, Kcnk3 channels open and close in two phases, one appears to be immediate and one is time-dependent (tau = approximately 5 ms). Both proton block and gating are potassium-sensitive; this produces an anomalous increase in outward flux as external potassium levels rise because of decreased proton block. Single Kcnk3 channels open across the physiological voltage range; hence they are "leak" conductances; however, they open only briefly and rarely even after exposure to agents that activate other potassium channels.

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Species referenced: Xenopus laevis
Genes referenced: kcnk3 mapt