Tok1p is a highly specific yeast plasma membrane potassium channel with strong outward directionality. Its opening is induced by membrane depolarization. Although the biophysical properties of Tok1p are well-described, its potentially important physiological role is currently largely unexplored. To address this issue, we examined the Tok1p activity following chemically-induced depolarization by measuring changes of plasma membrane potential (ΔΨ) using the diS-C(3) fluorescence assay in a Tok1p-expressing and a Tok1p-deficient strain. We report that Tok1p channel activity in response to chemical stress does not depend solely on the extent of depolarization, as might have been expected, but may also be negatively influenced by accompanying effects of the used compound. The stressors may interact with the plasma membrane or the channel itself, or cause cytosolic acidification. All of these effects may negatively influence the Tok1p channel opening. While ODDC-induced depolarization exhibits the cleanest Tok1p activation, restoring an astonishing 75% of lost ΔΨ, higher BAC concentrations reduce Tok1p activity, probably because of direct interactions with the channel and/or its lipid microenvironment. This is not only the first study of the physiological role of Tok1p in ΔΨ maintenance under chemical stress, but also the first estimate of the extent of depolarization the channel is able to counterbalance.
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http://dx.doi.org/10.1016/j.bbamem.2017.06.019 | DOI Listing |
Int J Mol Sci
September 2024
Laboratory of Oral Microbiology (LMO), Clinical University of Odontology (CLUO), University of Oviedo, 33006 Oviedo, Asturias, Spain.
Human lactoferrin (hLf) is an innate host defense protein that inhibits microbial H-ATPases. This protein includes an ancestral structural motif (i.e.
View Article and Find Full Text PDFInt J Mol Sci
July 2024
Laboratory of Oral Microbiology (LMO), University Clinic of Dentistry (CLUO), University of Oviedo, 33006 Oviedo, Asturias, Spain.
Human defensins are cysteine-rich peptides (Cys-rich peptides) of the innate immune system. Defensins contain an ancestral structural motif (i.e.
View Article and Find Full Text PDFInt J Mol Sci
November 2019
Laboratory of Oral Microbiology, University Clinic of Dentistry (CLUO), and Department of Functional Biology (Microbiology), Faculty of Medicine, University of Oviedo, 33006 Oviedo, Asturias, Spain.
In yeast, we reported the critical role of K-efflux for the progress of the regulated cell death (RCD) induced by human lactoferrin (hLf), an antimicrobial protein of the innate immune system that blocks Pma1p H-ATPase. In the present study, the K channel Tok1p was identified as the K channel-mediating K-efflux, as indicated by the protective effect of extracellular K (30 mM), K-channel blockers, and the greater hLf-resistance of -disrupted strains. K-depletion was necessary but not sufficient to induce RCD as inferred from the effects of valinomycin, NHCl or nigericin which released a percentage of K similar to that released by lactoferrin without affecting cell viability.
View Article and Find Full Text PDFBiochim Biophys Acta Biomembr
October 2017
Charles University, Faculty of Mathematics and Physics, Institute of Physics, Prague 121 16, Czech Republic. Electronic address:
Tok1p is a highly specific yeast plasma membrane potassium channel with strong outward directionality. Its opening is induced by membrane depolarization. Although the biophysical properties of Tok1p are well-described, its potentially important physiological role is currently largely unexplored.
View Article and Find Full Text PDFPflugers Arch
August 2008
Botanisches Institut I, Universität Karlsruhe (TH), Kaiserstrasse 12, 76128, Karlsruhe, Germany.
Tandem pore-loop potassium channels differ from the majority of K(+) channels in that a single polypeptide chain carries two K(+)-specific segments (P) each sandwiched between two transmembrane helices (M) to form an MP(1)M-MP(2)M series. Two of these peptide molecules assemble to form one functional potassium channel, which is expected to have biaxial symmetry (commonly described as asymmetric) due to independent mutation in the two MPM units. The resulting intrinsic asymmetry is exaggerated in fungal 2P channels, especially in Tok1p of Saccharomyces, by the N-terminal presence of four more transmembrane helices.
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