The kinetic transitions of proton-activated WT KcsA and the noninactivating E71A mutant were studied at the single-channel level in purified, liposome-reconstituted preparations. Single-channel currents were recorded using patch-clamp techniques under nonstationary and steady-state conditions. Maximum-likelihood analyses reveal that the key influence of acidic pH is to increase the frequency of bursting without an effect on the intraburst open and closed dwell times, consistent with the finding from macroscopic currents that protons promote activation without a significant effect on inactivation. However, in steady-conditions of pH, voltage not only alters the burst frequency but also affects their properties, such as the frequency of the flickers and the dwell times of the closed and open states. This is to be expected if voltage modulates pathways connecting open and inactivated states. Upon opening, KcsA can enter at least two closed states that are not part of the activation pathway. The frequency and duration of these closed states was found to be voltage dependent and therefore these are likely to represent short-lived inactivated states. Single-channel recordings of WT KcsA also show varying propensity for the presence of subconductance states. The probability of occurrence of these states did not show clear modulation by voltage or pH and their origin remains unclear and a focus for further investigation. A kinetic model is proposed to describe the gating events in KcsA that recapitulates its macroscopic and single-channel behavior. The model has been constrained by the single-channel analyses presented in this work along with data from macroscopic currents in the preceding paper.
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1 November 2007
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October 15 2007
A Quantitative Description of KcsA Gating II: Single-Channel Currents
Sudha Chakrapani,
Sudha Chakrapani
1Institute of Molecular Pediatrics Science and Department of Biochemistry and Molecular Biology, University of Chicago, Center for Integrative Science, Chicago, IL 60637
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Julio F Cordero-Morales,
Julio F Cordero-Morales
1Institute of Molecular Pediatrics Science and Department of Biochemistry and Molecular Biology, University of Chicago, Center for Integrative Science, Chicago, IL 60637
2Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA 22018
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Eduardo Perozo
Eduardo Perozo
1Institute of Molecular Pediatrics Science and Department of Biochemistry and Molecular Biology, University of Chicago, Center for Integrative Science, Chicago, IL 60637
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Sudha Chakrapani
1Institute of Molecular Pediatrics Science and Department of Biochemistry and Molecular Biology, University of Chicago, Center for Integrative Science, Chicago, IL 60637
Julio F Cordero-Morales
1Institute of Molecular Pediatrics Science and Department of Biochemistry and Molecular Biology, University of Chicago, Center for Integrative Science, Chicago, IL 60637
2Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA 22018
Eduardo Perozo
1Institute of Molecular Pediatrics Science and Department of Biochemistry and Molecular Biology, University of Chicago, Center for Integrative Science, Chicago, IL 60637
Correspondence to Eduardo Perozo: [email protected]
Abbreviations used in this paper: TM, transmembrane; WT, wild type.
Received:
June 13 2007
Accepted:
September 20 2007
Online ISSN: 1540-7748
Print ISSN: 0022-1295
The Rockefeller University Press
2007
J Gen Physiol (2007) 130 (5): 479–496.
Article history
Received:
June 13 2007
Accepted:
September 20 2007
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Sudha Chakrapani, Julio F Cordero-Morales, Eduardo Perozo; A Quantitative Description of KcsA Gating II: Single-Channel Currents . J Gen Physiol 1 November 2007; 130 (5): 479–496. doi: https://doi.org/10.1085/jgp.200709844
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