The Journal of General Physiology
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Published online April 30, 2007
doi:10.1085/jgp.200709774
The Journal of General Physiology, Vol. 129, No. 5, 437-455
The Rockefeller University Press, 0022-1295 $30.00
© 2007 Claydon et al.
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ARTICLE

A Direct Demonstration of Closed-State Inactivation of K+ Channels at Low pH



Thomas W. Claydon1, Moni Vaid2, Saman Rezazadeh2, Daniel C.H. Kwan2, Steven J. Kehl2, and David Fedida1,2

1 Department of Anesthesiology, Pharmacology, and Therapeutics and 2 Department of Cellular and Physiological Sciences, University of British Columbia, Vancouver, V6T 1Z3 Canada

Correspondence to David Fedida: fedida{at}interchange.ubc.ca

Lowering external pH reduces peak current and enhances current decay in Kv and Shaker-IR channels. Using voltage-clamp fluorimetry we directly determined the fate of Shaker-IR channels at low pH by measuring fluorescence emission from tetramethylrhodamine-5-maleimide attached to substituted cysteine residues in the voltage sensor domain (M356C to R362C) or S5-P linker (S424C). One aspect of the distal S3-S4 linker {alpha}-helix (A359C and R362C) reported a pH-induced acceleration of the slow phase of fluorescence quenching that represents P/C-type inactivation, but neither site reported a change in the total charge movement at low pH. Shaker S424C fluorescence demonstrated slow unquenching that also reflects channel inactivation and this too was accelerated at low pH. In addition, however, acidic pH caused a reversible loss of the fluorescence signal (pKa = 5.1) that paralleled the reduction of peak current amplitude (pKa = 5.2). Protons decreased single channel open probability, suggesting that the loss of fluorescence at low pH reflects a decreased channel availability that is responsible for the reduced macroscopic conductance. Inhibition of inactivation in Shaker S424C (by raising external K+ or the mutation T449V) prevented fluorescence loss at low pH, and the fluorescence report from closed Shaker ILT S424C channels implied that protons stabilized a W434F-like inactivated state. Furthermore, acidic pH changed the fluorescence amplitude (pKa = 5.9) in channels held continuously at –80 mV. This suggests that low pH stabilizes closed-inactivated states. Thus, fluorescence experiments suggest the major mechanism of pH-induced peak current reduction is inactivation of channels from closed states from which they can activate, but not open; this occurs in addition to acceleration of P/C-type inactivation from the open state.


Abbreviations used in this paper: PMT, photomultiplier tube; TMRM, tetramethylrhodamine-5-maleimide.


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