The Journal of General Physiology
Scientifica: Experts in Electrophysiology
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

This Article
Right arrow Full Text (PDF, 1851K)
Right arrow Alert me when this article is cited
Right arrow Citation Map
Services
Right arrow Email this article
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new content in the JGP
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Neyton, J.
Right arrow Articles by Pelleschi, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Neyton, J.
Right arrow Articles by Pelleschi, M.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?

The Journal of General Physiology, Vol 97, 641-665, Copyright © 1991 by The Rockefeller University Press


ARTICLES

Multi-ion occupancy alters gating in high-conductance, Ca(2+)-activated K+ channels

J Neyton and M Pelleschi
Laboratoire de Neurobiologie (URA 295 CNRS), Ecole Normale Superieure, Paris, France.

In this study, single-channel recordings of high-conductance Ca(2+)- activated K+ channels from rat skeletal muscle inserted into planar lipid bilayer were used to analyze the effects of two ionic blockers, Ba2+ and Na+, on the channel's gating reactions. The gating equilibrium of the Ba(2+)-blocked channel was investigated through the kinetics of the discrete blockade induced by Ba2+ ions. Gating properties of Na(+)- blocked channels could be directly characterized due to the very high rates of Na+ blocking/unblocking reactions. While in the presence of K+ (5 mM) in the external solution Ba2+ is known to stabilize the open state of the blocked channel (Miller, C., R. Latorre, and I. Reisin. 1987. J. Gen. Physiol. 90:427-449), we show that the divalent blocker stabilizes the closed-blocked state if permeant ions are removed from the external solution (K+ less than 10 microM). Ionic substitutions in the outer solution induce changes in the gating equilibrium of the Ba(2+)-blocked channel that are tightly correlated to the inhibition of Ba2+ dissociation by external monovalent cations. In permeant ion-free external solutions, blockade of the channel by internal Na+ induces a shift (around 15 mV) in the open probability--voltage curve toward more depolarized potentials, indicating that Na+ induces a stabilization of the closed-blocked state, as does Ba2+ under the same conditions. A kinetic analysis of the Na(+)-blocked channel indicates that the closed- blocked state is favored mainly by a decrease in opening rate. Addition of 1 mM external K+ completely inhibits the shift in the activation curve without affecting the Na(+)-induced reduction in the apparent single-channel amplitude. The results suggest that in the absence of external permeant ions internal blockers regulate the permeant ion occupancy of a site near the outer end of the channel. Occupancy of this site appears to modulate gating primarily by speeding the rate of channel opening.
Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?


This article has been cited by other articles:


Home page
JGPHome page
C. M. Wilkens and R. W. Aldrich
State-independent Block of BK Channels by an Intracellular Quaternary Ammonium
J. Gen. Physiol., August 28, 2006; 128(3): 347 - 364.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
R. A. Piskorowski and R. W. Aldrich
Relationship between Pore Occupancy and Gating in BK Potassium Channels
J. Gen. Physiol., April 24, 2006; 127(5): 557 - 576.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
J. F. Consiglio and S. J. Korn
Influence of Permeant Ions on Voltage Sensor Function in the Kv2.1 Potassium Channel
J. Gen. Physiol., March 29, 2004; 123(4): 387 - 400.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
A Molina, P Ortega-Saenz, and J Lopez-Barneo
Pore mutations alter closing and opening kinetics in Shaker K+ channels
J. Physiol., June 1, 1998; 509(2): 327 - 337.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
E. Drakopoulou, S. Zinn-Justin, M. Guenneugues, B. Gilquin, A. Ménez, and C. Vita
Changing the Structural Context of a Functional beta-Hairpin
J. Biol. Chem., May 17, 1996; 271(20): 11979 - 11987.
[Abstract] [Full Text] [PDF]



  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents