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

Biophysical Journal 54: 945-954 (1988)
© 1988 the Biophysical Society

This Article
Right arrow Full Text (PDF)
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 Campbell, D L
Right arrow Articles by Strauss, H C
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Campbell, D L
Right arrow Articles by Strauss, H C

Theoretical study of the voltage and concentration dependence of the anomalous mole fraction effect in single calcium channels. New insights into the characterization of multi-ion channels.

D L Campbell, R L Rasmusson and H C Strauss

Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.

ABSTRACT

Several recent independent studies on macroscopic Ca currents have demonstrated the anomalous mole fraction effect in mixtures of Ca and Ba at concentrations of 10 mM or less. Recently, Hess and Tsien (1984; Nature 309) proposed a dual binding site model, based upon Eyring rate theory, to account for this effect in L-type cardiac Ca channels. This model predicts that the anomalous mole fraction effect can be accounted for solely in terms of open single channel permeation properties; it was able to adequately reproduce the effect for macroscopic Ca currents recorded in 10 mM solutions. However, the electrochemical gradients under which single Ca channel current recordings are routinely made with the patch clamp technique vary dramatically from those used for macroscopic Ca currents. To properly assess the general validity of the Hess and Tsien model at the single Ca channel level, the effects of both large electrical potentials and elevated divalent concentrations must be understood. Computer simulations were therefore carried out using the original parameters used by Hess and Tsien under conditions designed to mimic those used in patch clamp studies. The permeation behavior generated by this model is quite complex. In particular, hyperpolarization and increased divalent concentration combine to reduce and ultimately abolish the anomalous mole fraction effect. It may therefore be very difficult to observe the anomalous mole fraction effect at the single Ca channel level; the dual-site model displays a relationship between current and mole fraction generally associated with a single-site model under the conditions frequently employed to resolve single Ca channel activity. Nonetheless, analysis of such monotonic mole fraction behavior can still be used as a test for the general validity of the dual-site model. Apparent Kms for Ca and Ba can be extracted from such monotonic behavior, and may not only be functions of membrane potential but may also depend upon the total divalent cation concentration. This is a unique prediction which is incompatible with the simple single-site model. Our analysis provides (a) a possible resolution for the apparent discrepancies presently existing in the experimental literature regarding the existence of the anomalous mole fraction effect at the single Ca channel level, (b) a mechanistic description of previously unexplained observations on the voltage-dependence of the anomalous mole fraction effect, and (c) a useful theoretical framework for future experimentation designed to test the general validity of the dual binding site model of the Ca channel.




This article has been cited by other articles:


Home page
J. Gen. Physiol.Home page
T. Cens, M. Rousset, A. Kajava, and P. Charnet
Molecular Determinant for Specific Ca/Ba Selectivity Profiles of Low and High Threshold Ca2+ Channels
J. Gen. Physiol., September 24, 2007; 130(4): 415 - 425.
[Abstract] [Full Text] [PDF]


Home page
Biophys. JHome page
X. Wang, T. A. Ponoran, R. L. Rasmusson, D. S. Ragsdale, and B. Z. Peterson
Amino Acid Substitutions in the Pore of the CaV1.2 Calcium Channel Reduce Barium Currents without Affecting Calcium Currents
Biophys. J., September 1, 2005; 89(3): 1731 - 1743.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
K. Talavera, M. Staes, A. Janssens, N. Klugbauer, G. Droogmans, F. Hofmann, and B. Nilius
Aspartate Residues of the Glu-Glu-Asp-Asp (EEDD) Pore Locus Control Selectivity and Permeation of the T-type Ca2+ Channel alpha 1G
J. Biol. Chem., November 30, 2001; 276(49): 45628 - 45635.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
A. Rodriguez-Contreras, W. Nonner, and E. N. Yamoah
Ca2+ transport properties and determinants of anomalous mole fraction effects of single voltage-gated Ca2+ channels in hair cells from bullfrog saccule
J. Physiol., February 1, 2002; 538(3): 729 - 745.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 1988 by the Biophysical Society.