Literature DB >> 14581587

Electrostatic control and chloride regulation of the fast gating of ClC-0 chloride channels.

Tsung-Yu Chen1, Mei-Fang Chen, Chia-Wei Lin.   

Abstract

The opening and closing of chloride (Cl-) channels in the ClC family are thought to tightly couple to ion permeation through the channel pore. In the prototype channel of the family, the ClC-0 channel from the Torpedo electric organ, the opening-closing of the pore in the millisecond time range known as "fast gating" is regulated by both external and internal Cl- ions. Although the external Cl- effect on the fast-gate opening has been extensively studied at a quantitative level, the internal Cl- regulation remains to be characterized. In this study, we examine the internal Cl- effects and the electrostatic controls of the fast-gating mechanism. While having little effect on the opening rate, raising [Cl-]i reduces the closing rate (or increases the open time) of the fast gate, with an apparent affinity of >1 M, a value very different from the one observed in the external Cl- regulation on the opening rate. Mutating charged residues in the pore also changes the fast-gating properties-the effects are more prominent on the closing rate than on the opening rate, a phenomenon similar to the effect of [Cl-]i on the fast gating. Thus, the alteration of fast-gate closing by charge mutations may come from a combination of two effects: a direct electrostatic interaction between the manipulated charge and the negatively charged glutamate gate and a repulsive force on the gate mediated by the permeant ion. Likewise, the regulations of internal Cl- on the fast gating may also be due to the competition of Cl- with the glutamate gate as well as the overall more negative potential brought to the pore by the binding of Cl-. In contrast, the opening rate of the fast gate is only minimally affected by manipulations of [Cl-]i and charges in the inner pore region. The very different nature of external and internal Cl- regulations on the fast gating thus may suggest that the opening and the closing of the fast gate are not microscopically reversible processes, but form a nonequilibrium cycle in the ClC-0 fast-gating mechanism.

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Year:  2003        PMID: 14581587      PMCID: PMC2229583          DOI: 10.1085/jgp.200308846

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


  30 in total

1.  Side-chain charge effects and conductance determinants in the pore of ClC-0 chloride channels.

Authors:  Mei-Fang Chen; Tsung-Yu Chen
Journal:  J Gen Physiol       Date:  2003-08       Impact factor: 4.086

2.  Steady-state coupling of ion-channel conformations to a transmembrane ion gradient.

Authors:  E A Richard; C Miller
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3.  Elimination of the slow gating of ClC-0 chloride channel by a point mutation.

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Journal:  J Gen Physiol       Date:  1999-07       Impact factor: 4.086

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Authors:  O P Hamill; A Marty; E Neher; B Sakmann; F J Sigworth
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5.  K+ channels close more slowly in the presence of external K+ and Rb+.

Authors:  R P Swenson; C M Armstrong
Journal:  Nature       Date:  1981-06-04       Impact factor: 49.962

6.  A voltage-gated anion channel from the electric organ of Torpedo californica.

Authors:  M M White; C Miller
Journal:  J Biol Chem       Date:  1979-10-25       Impact factor: 5.157

7.  Probing the pore of ClC-0 by substituted cysteine accessibility method using methane thiosulfonate reagents.

Authors:  Chia-Wei Lin; Tsung-Yu Chen
Journal:  J Gen Physiol       Date:  2003-08       Impact factor: 4.086

8.  Open-state substructure of single chloride channels from Torpedo electroplax.

Authors:  C Miller
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  1982-12-01       Impact factor: 6.237

9.  Single chloride channels from Torpedo electroplax. Activation by protons.

Authors:  W Hanke; C Miller
Journal:  J Gen Physiol       Date:  1983-07       Impact factor: 4.086

10.  Probes of the conduction process of a voltage-gated Cl- channel from Torpedo electroplax.

Authors:  M M White; C Miller
Journal:  J Gen Physiol       Date:  1981-07       Impact factor: 4.086

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  14 in total

1.  A three-state multi-ion kinetic model for conduction properties of ClC-0 chloride channel.

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2.  The fast gating mechanism in ClC-0 channels.

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Journal:  Biophys J       Date:  2005-04-29       Impact factor: 4.033

3.  Accessibility of the CLC-0 pore to charged methanethiosulfonate reagents.

Authors:  Xiao-Dong Zhang; Wei-Ping Yu; Tsung-Yu Chen
Journal:  Biophys J       Date:  2010-02-03       Impact factor: 4.033

Review 4.  A tale of two CLCs: biophysical insights toward understanding ClC-5 and ClC-7 function in endosomes and lysosomes.

Authors:  Giovanni Zifarelli
Journal:  J Physiol       Date:  2015-06-26       Impact factor: 5.182

5.  Roles of K149, G352, and H401 in the channel functions of ClC-0: testing the predictions from theoretical calculations.

Authors:  Xiao-Dong Zhang; Yong Li; Wei-Ping Yu; Tsung-Yu Chen
Journal:  J Gen Physiol       Date:  2006-04       Impact factor: 4.086

6.  Cysteine accessibility in ClC-0 supports conservation of the ClC intracellular vestibule.

Authors:  Anita M Engh; Merritt Maduke
Journal:  J Gen Physiol       Date:  2005-05-16       Impact factor: 4.086

7.  Exterior site occupancy infers chloride-induced proton gating in a prokaryotic homolog of the ClC chloride channel.

Authors:  David L Bostick; Max L Berkowitz
Journal:  Biophys J       Date:  2004-09       Impact factor: 4.033

8.  Intracellular proton regulation of ClC-0.

Authors:  Giovanni Zifarelli; Anna Rosa Murgia; Paolo Soliani; Michael Pusch
Journal:  J Gen Physiol       Date:  2008-07       Impact factor: 4.086

9.  Regulatory phosphorylation induces extracellular conformational changes in a CLC anion channel.

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Journal:  Biophys J       Date:  2013-05-07       Impact factor: 4.033

10.  Application of rate-equilibrium free energy relationship analysis to nonequilibrium ion channel gating mechanisms.

Authors:  László Csanády
Journal:  J Gen Physiol       Date:  2009-08       Impact factor: 4.086

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