help button home button Biophys. J.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Originally published as Biophys J. BioFAST on December 2, 2005.
doi:10.1529/biophysj.105.068577
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
biophysj.105.068577v1
90/4/1212    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Kwan, D. C. H.
Right arrow Articles by Kehl, S. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kwan, D. C. H.
Right arrow Articles by Kehl, S. J.
Biophysical Journal 90:1212-1222 (2006)
© 2006 The Biophysical Society

Single Channel Analysis Reveals Different Modes of Kv1.5 Gating Behavior Regulated by Changes of External pH

Daniel C. H. Kwan, David Fedida and Steven J. Kehl

Department of Cellular and Physiological Sciences, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3

Correspondence: Address reprint requests to S. J. Kehl, Tel.: 604-822-2185; Fax: 604-822-2316; E-mail: skehl{at}interchange.ubc.ca.

In the voltage-gated potassium channel Kv1.5, extracellular acidification decreases the peak macroscopic conductance and accelerates slow inactivation. To better understand the mechanistic basis for these two effects, we recorded unitary currents of Kv1.5 expressed in a mouse cell line (ltk) using the voltage clamp technique both in cell-attached and excised outside-out patches. Single channel current amplitude at 100 mV (1.7 ± 0.2 pA at pH 7.4, 1.7 ± 0.2 pA at pH 6.4) and the single channel conductance between 0 and 100 mV (11.8 ± 0.6 pS at pH 7.4 and 11.3 ± 0.8 pS at pH 6.4) did not change significantly with pH. External acidification significantly decreased the number of active sweeps, and this reduction in channel availability accounted for most of the reduction of the peak macroscopic current. The results of runs analyses suggested the null sweeps occur in clusters, and the rate constants for the transition between clusters of null and active sweeps at pH 6.4 were slow (0.12 and 0.18 s–1, to and from the active clusters, respectively). We propose that low pH facilitates a shift from an available mode (mode A) into an unavailable mode of gating (mode U). In addition to promoting mode U gating, external acidification accelerates depolarization-induced inactivation, which is manifest at the single channel level as a reduction of the mean burst length and an apparent increase of the interburst interval. These effects of external acidification, which are thought to reflect the protonation of a histidine residue in the turret (H-463), point to an important role for the turret in the regulation of channel availability and inactivation.




This article has been cited by other articles:


Home page
J. Gen. Physiol.Home page
T. W. Claydon, M. Vaid, S. Rezazadeh, D. C.H. Kwan, S. J. Kehl, and D. Fedida
A Direct Demonstration of Closed-State Inactivation of K+ Channels at Low pH
J. Gen. Physiol., April 30, 2007; 129(5): 437 - 455.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
W. Treptow and M. Tarek
K+ Conduction in the Selectivity Filter of Potassium Channels Is Monitored by the Charge Distribution along Their Sequence
Biophys. J., November 15, 2006; 91(10): L81 - L83.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2006 by the Biophysical Society.