The Journal of General Physiology
Cell MicroControls
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Published online
doi:10.1085/jgp.200810004
The Journal of General Physiology, Vol. 133, No. 1, 43-58
The Rockefeller University Press, 0022-1295 $30.00
© Zhang et al.
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ARTICLE

Blocking Pore-open Mutants of CLC-0 by Amphiphilic Blockers



Xiao-Dong Zhang, Pang-Yen Tseng, Wei-Ping Yu, and Tsung-Yu Chen

Center for Neuroscience and Department of Neurology, University of California, Davis, Davis, CA 95618

Correspondence to Tsung-Yu Chen: tycchen{at}ucdavis.edu

The blockade of CLC-0 chloride channels by p-chlorophenoxy acetate (CPA) has been thought to be state dependent; the conformational change of the channel pore during the "fast gating" alters the CPA binding affinity. Here, we examine the mechanism of CPA blocking in pore-open mutants of CLC-0 in which the residue E166 was replaced by various amino acids. We find that the CPA-blocking affinities depend upon the volume and the hydrophobicity of the side chain of the introduced residue; CPA affinity can vary by three orders of magnitude in these mutants. On the other hand, mutations at the intracellular pore entrance, although affecting the association and dissociation rates of the CPA block, generate only a modest effect on the steady-state blocking affinity. In addition, various amphiphilic compounds, including fatty acids and alkyl sulfonates, can also block the pore-open mutants of CLC-0 through a similar mechanism. The blocking affinity of fatty acids and alkyl sulfonates increases with the length of these amphiphilic blockers, a phenomenon similar to the block of the Shaker K+ channel by long-chain quaternary ammonium (QA) ions. These observations lead us to propose that the CPA block of the open pore of CLC-0 is similar to the blockade of voltage-gated K+ channels by long-chain QAs or by the inactivation ball peptide: the blocker first uses the hydrophilic end to "dock" at the pore entrance, and the hydrophobic part of the blocker then enters the pore to interact with a more hydrophobic region of the pore. This blocking mechanism appears to be very general because the block does not require a precise structural fit between the blocker and the pore, and the blocking mechanism applies to the cation and anion channels with unrelated pore architectures.


Abbreviations used in this paper: CB, closed and blocked; CPA, p-chlorophenoxy acetate; HEK, human embryonic kidney; MTS, methanethiolsulfonate; OB, open and blocked; QA, quaternary ammonium.

© 2009 Zhang 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.jgp.org/misc/terms.shtml). 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/).


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Related Article

Amphiphilic Blockers Punch through a Mutant CLC-0 Pore
Xiao-Dong Zhang and Tsung-Yu Chen
J. Gen. Physiol. 2008 133: 59-68. [Abstract] [Full Text] [PDF]





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