The Journal of General Physiology
  Home | Help | Feedback | Subscriptions | Archive | Search | Table of Contents

This Article
Right arrow Full Text
Right arrow Full Text (PDF, 398K)
Right arrow PPT slides of all figures
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 Sunderman, E. R.
Right arrow Articles by Zagotta, W. N.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sunderman, E. R.
Right arrow Articles by Zagotta, W. N.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?
© The Rockefeller University Press, 0022-1295/1999//621/ $5.00
Journal of General Physiology, Volume 113, Number 5, 1999


Article

Sequence of Events Underlying the Allosteric Transition of Rod Cyclic Nucleotide–gated Channels

Elizabeth R. Sunderman and William N. Zagotta

From the Department of Physiology and Biophysics, Howard Hughes Medical Institute, University of Washington, Seattle, Washington 98195

Activation of cyclic nucleotide–gated (CNG) ion channels involves a conformational change in the channel protein referred to as the allosteric transition. The amino terminal region and the carboxyl terminal cyclic nucleotide–binding domain of CNG channels have been shown to be involved in the allosteric transition, but the sequence of molecular events occurring during the allosteric transition is unknown. We recorded single-channel currents from bovine rod CNG channels in which mutations had been introduced in the binding domain at position 604 and/or the rat olfactory CNG channel amino terminal region had been substituted for the bovine rod amino terminal region. Using a hidden Markov modeling approach, we analyzed the kinetics of these channels activated by saturating concentrations of cGMP, cIMP, and cAMP. We used thermodynamic mutant cycles to reveal an interaction during the allosteric transition between the purine ring of the cyclic nucleotides and the amino acid at position 604 in the binding site. We found that mutations at position 604 in the binding domain alter both the opening and closing rate constants for the allosteric transition, indicating that the interactions between the cyclic nucleotide and this amino acid are partially formed at the time of the transition state. In contrast, the amino terminal region affects primarily the closing rate constant for the allosteric transition, suggesting that the state-dependent stabilizing interactions between amino and carboxyl terminal regions are not formed at the time of the transition state for the allosteric transition. We propose that the sequence of events that occurs during the allosteric transition involves the formation of stabilizing interactions between the purine ring of the cyclic nucleotide and the amino acid at position 604 in the binding domain followed by the formation of stabilizing interdomain interactions.

Key Words: electrophysiology • ion channel gating • kinetics • cyclic GMP • open probability


Abbreviations: BROD, bovine rod; CAP, catabolite gene activator protein; CNG, cyclic nucleotide–gated; HMM, hidden Markov model


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 Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
JGPHome page
L. Hua and S. E. Gordon
Functional Interactions Between A' Helices in the C-linker of Open CNG Channels
J. Gen. Physiol., February 28, 2005; 125(3): 335 - 344.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
J. P. Johnson Jr. and W. N. Zagotta
The carboxyl-terminal region of cyclic nucleotide-modulated channels is a gating ring, not a permeation path
PNAS, February 22, 2005; 102(8): 2742 - 2747.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
E. C. Young and N. Krougliak
Distinct Structural Determinants of Efficacy and Sensitivity in the Ligand-binding Domain of Cyclic Nucleotide-gated Channels
J. Biol. Chem., January 30, 2004; 279(5): 3553 - 3562.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. L. Krajewski, C. W. Luetje, and R. H. Kramer
Tyrosine Phosphorylation of Rod Cyclic Nucleotide-Gated Channels Switches Off Ca2+/Calmodulin Inhibition
J. Neurosci., November 5, 2003; 23(31): 10100 - 10106.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
D. Enkvetchakul and C.G. Nichols
Gating Mechanism of KATP Channels: Function Fits Form
J. Gen. Physiol., October 27, 2003; 122(5): 471 - 480.
[Full Text] [PDF]


Home page
JGPHome page
J. Zheng, L. Vankataramanan, and F. J. Sigworth
Hidden Markov Model Analysis of Intermediate Gating Steps Associated with the Pore Gate of Shaker Potassium Channels
J. Gen. Physiol., November 1, 2001; 118(5): 547 - 564.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
E. C. Young, D. M. Sciubba, and S. A. Siegelbaum
Efficient Coupling of Ligand Binding to Channel Opening by the Binding Domain of a Modulatory ({beta}) Subunit of the Olfactory Cyclic Nucleotide-Gated Channel
J. Gen. Physiol., November 1, 2001; 118(5): 523 - 546.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
P. Gavazzo, C. Picco, E. Eismann, U. B. Kaupp, and A. Menini
A Point Mutation in the Pore Region Alters Gating, Ca2+Blockage, and Permeation of Olfactory Cyclic Nucleotide-Gated Channels
J. Gen. Physiol., September 1, 2000; 116(3): 311 - 326.
[Abstract] [Full Text] [PDF]


Home page
JGPHome page
D. Guo and Z. Lu
Mechanism of Cgmp-Gated Channel Block by Intracellular Polyamines
J. Gen. Physiol., June 1, 2000; 115(6): 783 - 798.
[Abstract] [Full Text] [PDF]



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