Cargando…

Distinct subunit contributions to the activation of M-type potassium channels by PI(4,5)P(2)

Low-threshold voltage-gated M-type potassium channels (M channels) are tetraheteromers, commonly of two Kv7.2 and two Kv7.3 subunits. Though gated by voltage, the channels have an absolute requirement for binding of the membrane phospholipid phosphatidylinositol-4,5-bisphosphate (PI(4,5)P(2)) to ope...

Descripción completa

Detalles Bibliográficos
Autores principales: Telezhkin, Vsevolod, Brown, David A., Gibb, Alasdair J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382723/
https://www.ncbi.nlm.nih.gov/pubmed/22689829
http://dx.doi.org/10.1085/jgp.201210796
_version_ 1782236533771730944
author Telezhkin, Vsevolod
Brown, David A.
Gibb, Alasdair J.
author_facet Telezhkin, Vsevolod
Brown, David A.
Gibb, Alasdair J.
author_sort Telezhkin, Vsevolod
collection PubMed
description Low-threshold voltage-gated M-type potassium channels (M channels) are tetraheteromers, commonly of two Kv7.2 and two Kv7.3 subunits. Though gated by voltage, the channels have an absolute requirement for binding of the membrane phospholipid phosphatidylinositol-4,5-bisphosphate (PI(4,5)P(2)) to open. We have investigated the quantitative relation between the concentration of a water-soluble PI(4,5)P(2) analog, dioctanoyl-PI(4,5)P(2) (DiC(8)-PI(4,5)P(2)), and channel open probability (P(open)) by fast application of increasing concentrations of DiC(8)-PI(4,5)P(2) to the inside face of membrane patches excised from Chinese hamster ovary cells expressing M channels as heteromeric Kv7.2/7.3 subunits. The rationale for the experiments is that this will mimic the effect of changes in membrane PI(4,5)P(2) concentration. Single-channel conductances from channel current–voltage relations in cell-attached mode were 9.2 ± 0.1 pS with a 2.5-mM pipette [K(+)]. Plots of P(open) against DiC(8)-PI(4,5)P(2) concentration were best fitted using a two-component concentration–P(open) relationship with high and low affinity, half-maximal effective concentration (EC(50)) values of 1.3 ± 0.14 and 75.5 ± 2.5 µM, respectively, and Hill slopes of 1.4 ± 0.06. In contrast, homomeric channels from cells expressing only Kv7.2 or Kv7.3 constructs yielded single-component curves with EC(50) values of 76.2 ± 19.9 or 3.6 ± 1.0 µM, respectively. When wild-type (WT) Kv7.2 was coexpressed with a mutated Kv7.3 subunit with >100-fold reduced sensitivity to PI(4,5)P(2), the high-affinity component of the activation curve was lost. Fitting the data for WT and mutant channels to an activation mechanism with independent PI(4,5)P(2) binding to two Kv7.2 and two Kv7.3 subunits suggests that the two components of the M-channel activation curve correspond to the interaction of PI(4,5)P(2) with the Kv7.3 and Kv7.2 subunits, respectively, that channels can open when only the two Kv7.3 subunits have bound DiC(8)-PI(4,5)P(2), and that maximum channel opening requires binding to all four subunits.
format Online
Article
Text
id pubmed-3382723
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-33827232013-01-01 Distinct subunit contributions to the activation of M-type potassium channels by PI(4,5)P(2) Telezhkin, Vsevolod Brown, David A. Gibb, Alasdair J. J Gen Physiol Article Low-threshold voltage-gated M-type potassium channels (M channels) are tetraheteromers, commonly of two Kv7.2 and two Kv7.3 subunits. Though gated by voltage, the channels have an absolute requirement for binding of the membrane phospholipid phosphatidylinositol-4,5-bisphosphate (PI(4,5)P(2)) to open. We have investigated the quantitative relation between the concentration of a water-soluble PI(4,5)P(2) analog, dioctanoyl-PI(4,5)P(2) (DiC(8)-PI(4,5)P(2)), and channel open probability (P(open)) by fast application of increasing concentrations of DiC(8)-PI(4,5)P(2) to the inside face of membrane patches excised from Chinese hamster ovary cells expressing M channels as heteromeric Kv7.2/7.3 subunits. The rationale for the experiments is that this will mimic the effect of changes in membrane PI(4,5)P(2) concentration. Single-channel conductances from channel current–voltage relations in cell-attached mode were 9.2 ± 0.1 pS with a 2.5-mM pipette [K(+)]. Plots of P(open) against DiC(8)-PI(4,5)P(2) concentration were best fitted using a two-component concentration–P(open) relationship with high and low affinity, half-maximal effective concentration (EC(50)) values of 1.3 ± 0.14 and 75.5 ± 2.5 µM, respectively, and Hill slopes of 1.4 ± 0.06. In contrast, homomeric channels from cells expressing only Kv7.2 or Kv7.3 constructs yielded single-component curves with EC(50) values of 76.2 ± 19.9 or 3.6 ± 1.0 µM, respectively. When wild-type (WT) Kv7.2 was coexpressed with a mutated Kv7.3 subunit with >100-fold reduced sensitivity to PI(4,5)P(2), the high-affinity component of the activation curve was lost. Fitting the data for WT and mutant channels to an activation mechanism with independent PI(4,5)P(2) binding to two Kv7.2 and two Kv7.3 subunits suggests that the two components of the M-channel activation curve correspond to the interaction of PI(4,5)P(2) with the Kv7.3 and Kv7.2 subunits, respectively, that channels can open when only the two Kv7.3 subunits have bound DiC(8)-PI(4,5)P(2), and that maximum channel opening requires binding to all four subunits. The Rockefeller University Press 2012-07 /pmc/articles/PMC3382723/ /pubmed/22689829 http://dx.doi.org/10.1085/jgp.201210796 Text en © 2012 Telezhkin et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).
spellingShingle Article
Telezhkin, Vsevolod
Brown, David A.
Gibb, Alasdair J.
Distinct subunit contributions to the activation of M-type potassium channels by PI(4,5)P(2)
title Distinct subunit contributions to the activation of M-type potassium channels by PI(4,5)P(2)
title_full Distinct subunit contributions to the activation of M-type potassium channels by PI(4,5)P(2)
title_fullStr Distinct subunit contributions to the activation of M-type potassium channels by PI(4,5)P(2)
title_full_unstemmed Distinct subunit contributions to the activation of M-type potassium channels by PI(4,5)P(2)
title_short Distinct subunit contributions to the activation of M-type potassium channels by PI(4,5)P(2)
title_sort distinct subunit contributions to the activation of m-type potassium channels by pi(4,5)p(2)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382723/
https://www.ncbi.nlm.nih.gov/pubmed/22689829
http://dx.doi.org/10.1085/jgp.201210796
work_keys_str_mv AT telezhkinvsevolod distinctsubunitcontributionstotheactivationofmtypepotassiumchannelsbypi45p2
AT browndavida distinctsubunitcontributionstotheactivationofmtypepotassiumchannelsbypi45p2
AT gibbalasdairj distinctsubunitcontributionstotheactivationofmtypepotassiumchannelsbypi45p2