Literature DB >> 9607935

Kinetic structure of large-conductance Ca2+-activated K+ channels suggests that the gating includes transitions through intermediate or secondary states. A mechanism for flickers.

B S Rothberg1, K L Magleby.   

Abstract

Mechanisms for the Ca2+-dependent gating of single large-conductance Ca2+-activated K+ channels from cultured rat skeletal muscle were developed using two-dimensional analysis of single-channel currents recorded with the patch clamp technique. To extract and display the essential kinetic information, the kinetic structure, from the single channel currents, adjacent open and closed intervals were binned as pairs and plotted as two-dimensional dwell-time distributions, and the excesses and deficits of the interval pairs over that expected for independent pairing were plotted as dependency plots. The basic features of the kinetic structure were generally the same among single large-conductance Ca2+-activated K+ channels, but channel-specific differences were readily apparent, suggesting heterogeneities in the gating. Simple gating schemes drawn from the Monod- Wyman-Changeux (MWC) model for allosteric proteins could approximate the basic features of the Ca2+ dependence of the kinetic structure. However, consistent differences between the observed and predicted dependency plots suggested that additional brief lifetime closed states not included in MWC-type models were involved in the gating. Adding these additional brief closed states to the MWC-type models, either beyond the activation pathway (secondary closed states) or within the activation pathway (intermediate closed states), improved the description of the Ca2+ dependence of the kinetic structure. Secondary closed states are consistent with the closing of secondary gates or channel block. Intermediate closed states are consistent with mechanisms in which the channel activates by passing through a series of intermediate conformations between the more stable open and closed states. It is the added secondary or intermediate closed states that give rise to the majority of the brief closings (flickers) in the gating.

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Year:  1998        PMID: 9607935      PMCID: PMC2217154          DOI: 10.1085/jgp.111.6.751

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  75 in total

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Authors:  P H Reinhart; S Chung; B L Martin; D L Brautigan; I B Levitan
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3.  Estimating kinetic parameters for single channels with simulation. A general method that resolves the missed event problem and accounts for noise.

Authors:  K L Magleby; D S Weiss
Journal:  Biophys J       Date:  1990-12       Impact factor: 4.033

4.  Use of conditioned distributions in the analysis of ion channel recordings.

Authors:  D Petracchi; M Barbi; M Pellegrini; M Pellegrino; A Simoni
Journal:  Eur Biophys J       Date:  1991       Impact factor: 1.733

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Authors:  N S Atkinson; G A Robertson; B Ganetzky
Journal:  Science       Date:  1991-08-02       Impact factor: 47.728

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Authors:  O B McManus
Journal:  J Bioenerg Biomembr       Date:  1991-08       Impact factor: 2.945

7.  Kinetic time constants independent of previous single-channel activity suggest Markov gating for a large conductance Ca-activated K channel.

Authors:  O B McManus; K L Magleby
Journal:  J Gen Physiol       Date:  1989-12       Impact factor: 4.086

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Authors:  A Marty
Journal:  Trends Neurosci       Date:  1989-11       Impact factor: 13.837

9.  Ion-channel gating mechanisms: model identification and parameter estimation from single channel recordings.

Authors:  F G Ball; M S Sansom
Journal:  Proc R Soc Lond B Biol Sci       Date:  1989-05-22

10.  Competitive Mg2+ block of a large-conductance, Ca(2+)-activated K+ channel in rat skeletal muscle. Ca2+, Sr2+, and Ni2+ also block.

Authors:  W B Ferguson
Journal:  J Gen Physiol       Date:  1991-07       Impact factor: 4.086

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  45 in total

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Authors:  Rebecca A Piskorowski; Richard W Aldrich
Journal:  J Gen Physiol       Date:  2006-05       Impact factor: 4.086

7.  Ca(2+)- and voltage-dependent gating of Ca(2+)- and ATP-sensitive cationic channels in brain capillary endothelium.

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8.  Short isoforms of the cold receptor TRPM8 inhibit channel gating by mimicking heat action rather than chemical inhibitors.

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9.  Stepwise contribution of each subunit to the cooperative activation of BK channels by Ca2+.

Authors:  Xiaowei Niu; Karl L Magleby
Journal:  Proc Natl Acad Sci U S A       Date:  2002-08-02       Impact factor: 11.205

10.  Desensitization contributes to the synaptic response of gain-of-function mutants of the muscle nicotinic receptor.

Authors:  Sergio Elenes; Ying Ni; Gisela D Cymes; Claudio Grosman
Journal:  J Gen Physiol       Date:  2006-11       Impact factor: 4.086

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