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Coupling and cooperativity in voltage activation of a limited-state BK channel gating in saturating Ca(2+)
Voltage-dependent gating mechanisms of large conductance Ca(2+) and voltage-activated (BK) channels were investigated using two-dimensional maximum likelihood analysis of single-channel open and closed intervals. To obtain sufficient data at negative as well as positive voltages, single-channel curr...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860587/ https://www.ncbi.nlm.nih.gov/pubmed/20421372 http://dx.doi.org/10.1085/jgp.200910331 |
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author | Shelley, Christopher Niu, Xiaowei Geng, Yanyan Magleby, Karl L. |
author_facet | Shelley, Christopher Niu, Xiaowei Geng, Yanyan Magleby, Karl L. |
author_sort | Shelley, Christopher |
collection | PubMed |
description | Voltage-dependent gating mechanisms of large conductance Ca(2+) and voltage-activated (BK) channels were investigated using two-dimensional maximum likelihood analysis of single-channel open and closed intervals. To obtain sufficient data at negative as well as positive voltages, single-channel currents were recorded at saturating Ca(2+) from BK channels mutated to remove the RCK1 Ca(2+) and Mg(2+) sensors. The saturating Ca(2+) acting on the Ca(2+) bowl sensors of the resulting BK(B) channels increased channel activity while driving the gating into a reduced number of states, simplifying the model. Five highly constrained idealized gating mechanisms based on extensions of the Monod-Wyman-Changeux model for allosteric proteins were examined. A 10-state model without coupling between the voltage sensors and the opening/closing transitions partially described the voltage dependence of Po but not the single-channel kinetics. With allowed coupling, the model gave improved descriptions of Po and approximated the single-channel kinetics; each activated voltage sensor increased the opening rate approximately an additional 23-fold while having little effect on the closing rate. Allowing cooperativity among voltage sensors further improved the description of the data: each activated voltage sensor increased the activation rate of the remaining voltage sensors approximately fourfold, with little effect on the deactivation rate. The coupling factor was decreased in models with cooperativity from ∼23 to ∼18. Whether the apparent cooperativity among voltage sensors arises from imposing highly idealized models or from actual cooperativity will require additional studies to resolve. For both cooperative and noncooperative models, allowing transitions to five additional brief (flicker) closed states further improved the description of the data. These observations show that the voltage-dependent single-channel kinetics of BK(B) channels can be approximated by highly idealized allosteric models in which voltage sensor movement increases Po mainly through an increase in channel opening rates, with limited effects on closing rates. |
format | Text |
id | pubmed-2860587 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-28605872010-11-01 Coupling and cooperativity in voltage activation of a limited-state BK channel gating in saturating Ca(2+) Shelley, Christopher Niu, Xiaowei Geng, Yanyan Magleby, Karl L. J Gen Physiol Article Voltage-dependent gating mechanisms of large conductance Ca(2+) and voltage-activated (BK) channels were investigated using two-dimensional maximum likelihood analysis of single-channel open and closed intervals. To obtain sufficient data at negative as well as positive voltages, single-channel currents were recorded at saturating Ca(2+) from BK channels mutated to remove the RCK1 Ca(2+) and Mg(2+) sensors. The saturating Ca(2+) acting on the Ca(2+) bowl sensors of the resulting BK(B) channels increased channel activity while driving the gating into a reduced number of states, simplifying the model. Five highly constrained idealized gating mechanisms based on extensions of the Monod-Wyman-Changeux model for allosteric proteins were examined. A 10-state model without coupling between the voltage sensors and the opening/closing transitions partially described the voltage dependence of Po but not the single-channel kinetics. With allowed coupling, the model gave improved descriptions of Po and approximated the single-channel kinetics; each activated voltage sensor increased the opening rate approximately an additional 23-fold while having little effect on the closing rate. Allowing cooperativity among voltage sensors further improved the description of the data: each activated voltage sensor increased the activation rate of the remaining voltage sensors approximately fourfold, with little effect on the deactivation rate. The coupling factor was decreased in models with cooperativity from ∼23 to ∼18. Whether the apparent cooperativity among voltage sensors arises from imposing highly idealized models or from actual cooperativity will require additional studies to resolve. For both cooperative and noncooperative models, allowing transitions to five additional brief (flicker) closed states further improved the description of the data. These observations show that the voltage-dependent single-channel kinetics of BK(B) channels can be approximated by highly idealized allosteric models in which voltage sensor movement increases Po mainly through an increase in channel opening rates, with limited effects on closing rates. The Rockefeller University Press 2010-05 /pmc/articles/PMC2860587/ /pubmed/20421372 http://dx.doi.org/10.1085/jgp.200910331 Text en © 2010 Shelley 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 Shelley, Christopher Niu, Xiaowei Geng, Yanyan Magleby, Karl L. Coupling and cooperativity in voltage activation of a limited-state BK channel gating in saturating Ca(2+) |
title | Coupling and cooperativity in voltage activation of a limited-state BK channel gating in saturating Ca(2+) |
title_full | Coupling and cooperativity in voltage activation of a limited-state BK channel gating in saturating Ca(2+) |
title_fullStr | Coupling and cooperativity in voltage activation of a limited-state BK channel gating in saturating Ca(2+) |
title_full_unstemmed | Coupling and cooperativity in voltage activation of a limited-state BK channel gating in saturating Ca(2+) |
title_short | Coupling and cooperativity in voltage activation of a limited-state BK channel gating in saturating Ca(2+) |
title_sort | coupling and cooperativity in voltage activation of a limited-state bk channel gating in saturating ca(2+) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2860587/ https://www.ncbi.nlm.nih.gov/pubmed/20421372 http://dx.doi.org/10.1085/jgp.200910331 |
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