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Functional Coupling of the β(1) Subunit to the Large Conductance Ca(2+)-Activated K(+) Channel in the Absence of Ca(2+) : Increased Ca(2+) Sensitivity from a Ca(2+)-Independent Mechanism
Coexpression of the β(1) subunit with the α subunit (mSlo) of BK channels increases the apparent Ca(2+) sensitivity of the channel. This study investigates whether the mechanism underlying the increased Ca(2+) sensitivity requires Ca(2+), by comparing the gating in 0 Ca(2+) (i) of BK channels compos...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2232893/ https://www.ncbi.nlm.nih.gov/pubmed/10828246 |
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author | Nimigean, Crina M. Magleby, Karl L. |
author_facet | Nimigean, Crina M. Magleby, Karl L. |
author_sort | Nimigean, Crina M. |
collection | PubMed |
description | Coexpression of the β(1) subunit with the α subunit (mSlo) of BK channels increases the apparent Ca(2+) sensitivity of the channel. This study investigates whether the mechanism underlying the increased Ca(2+) sensitivity requires Ca(2+), by comparing the gating in 0 Ca(2+) (i) of BK channels composed of α subunits to those composed of α+β(1) subunits. The β(1) subunit increased burst duration ∼20-fold and the duration of gaps between bursts ∼3-fold, giving an ∼10-fold increase in open probability (P (o)) in 0 Ca(2+) (i). The effect of the β(1) subunit on increasing burst duration was little changed over a wide range of P (o) achieved by varying either Ca(2+) (i) or depolarization. The effect of the β(1) subunit on increasing the durations of the gaps between bursts in 0 Ca(2+) (i) was preserved over a range of voltage, but was switched off as Ca(2+) (i) was increased into the activation range. The Ca(2+)-independent, β(1) subunit-induced increase in burst duration accounted for 80% of the leftward shift in the P (o) vs. Ca(2+) (i) curve that reflects the increased Ca(2+) sensitivity induced by the β(1) subunit. The Ca(2+)-dependent effect of the β(1) subunit on the gaps between bursts accounted for the remaining 20% of the leftward shift. Our observation that the major effects of the β(1) subunit are independent of Ca(2+) (i) suggests that the β(1) subunit mainly alters the energy barriers of Ca(2+)-independent transitions. The changes in gating induced by the β(1) subunit differ from those induced by depolarization, as increasing P (o) by depolarization or by the β(1) subunit gave different gating kinetics. The complex gating kinetics for both α and α+β(1) channels in 0 Ca(2+) (i) arise from transitions among two to three open and three to five closed states and are inconsistent with Monod-Wyman-Changeux type models, which predict gating among only one open and one closed state in 0 Ca(2+) (i). |
format | Text |
id | pubmed-2232893 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-22328932008-04-22 Functional Coupling of the β(1) Subunit to the Large Conductance Ca(2+)-Activated K(+) Channel in the Absence of Ca(2+) : Increased Ca(2+) Sensitivity from a Ca(2+)-Independent Mechanism Nimigean, Crina M. Magleby, Karl L. J Gen Physiol Original Article Coexpression of the β(1) subunit with the α subunit (mSlo) of BK channels increases the apparent Ca(2+) sensitivity of the channel. This study investigates whether the mechanism underlying the increased Ca(2+) sensitivity requires Ca(2+), by comparing the gating in 0 Ca(2+) (i) of BK channels composed of α subunits to those composed of α+β(1) subunits. The β(1) subunit increased burst duration ∼20-fold and the duration of gaps between bursts ∼3-fold, giving an ∼10-fold increase in open probability (P (o)) in 0 Ca(2+) (i). The effect of the β(1) subunit on increasing burst duration was little changed over a wide range of P (o) achieved by varying either Ca(2+) (i) or depolarization. The effect of the β(1) subunit on increasing the durations of the gaps between bursts in 0 Ca(2+) (i) was preserved over a range of voltage, but was switched off as Ca(2+) (i) was increased into the activation range. The Ca(2+)-independent, β(1) subunit-induced increase in burst duration accounted for 80% of the leftward shift in the P (o) vs. Ca(2+) (i) curve that reflects the increased Ca(2+) sensitivity induced by the β(1) subunit. The Ca(2+)-dependent effect of the β(1) subunit on the gaps between bursts accounted for the remaining 20% of the leftward shift. Our observation that the major effects of the β(1) subunit are independent of Ca(2+) (i) suggests that the β(1) subunit mainly alters the energy barriers of Ca(2+)-independent transitions. The changes in gating induced by the β(1) subunit differ from those induced by depolarization, as increasing P (o) by depolarization or by the β(1) subunit gave different gating kinetics. The complex gating kinetics for both α and α+β(1) channels in 0 Ca(2+) (i) arise from transitions among two to three open and three to five closed states and are inconsistent with Monod-Wyman-Changeux type models, which predict gating among only one open and one closed state in 0 Ca(2+) (i). The Rockefeller University Press 2000-06-01 /pmc/articles/PMC2232893/ /pubmed/10828246 Text en © 2000 The Rockefeller University Press 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 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Original Article Nimigean, Crina M. Magleby, Karl L. Functional Coupling of the β(1) Subunit to the Large Conductance Ca(2+)-Activated K(+) Channel in the Absence of Ca(2+) : Increased Ca(2+) Sensitivity from a Ca(2+)-Independent Mechanism |
title | Functional Coupling of the β(1) Subunit to the Large Conductance Ca(2+)-Activated K(+) Channel in the Absence of Ca(2+)
: Increased Ca(2+) Sensitivity from a Ca(2+)-Independent Mechanism |
title_full | Functional Coupling of the β(1) Subunit to the Large Conductance Ca(2+)-Activated K(+) Channel in the Absence of Ca(2+)
: Increased Ca(2+) Sensitivity from a Ca(2+)-Independent Mechanism |
title_fullStr | Functional Coupling of the β(1) Subunit to the Large Conductance Ca(2+)-Activated K(+) Channel in the Absence of Ca(2+)
: Increased Ca(2+) Sensitivity from a Ca(2+)-Independent Mechanism |
title_full_unstemmed | Functional Coupling of the β(1) Subunit to the Large Conductance Ca(2+)-Activated K(+) Channel in the Absence of Ca(2+)
: Increased Ca(2+) Sensitivity from a Ca(2+)-Independent Mechanism |
title_short | Functional Coupling of the β(1) Subunit to the Large Conductance Ca(2+)-Activated K(+) Channel in the Absence of Ca(2+)
: Increased Ca(2+) Sensitivity from a Ca(2+)-Independent Mechanism |
title_sort | functional coupling of the β(1) subunit to the large conductance ca(2+)-activated k(+) channel in the absence of ca(2+)
: increased ca(2+) sensitivity from a ca(2+)-independent mechanism |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2232893/ https://www.ncbi.nlm.nih.gov/pubmed/10828246 |
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