Prolonged depolarization induces a slow inactivation process in some K+ channels. We have studied ionic and gating currents during long depolarizations in the mutant Shaker H4-Δ(6–46) K+ channel and in the nonconducting mutant (Shaker H4-Δ(6–46)-W434F). These channels lack the amino terminus that confers the fast (N-type) inactivation (Hoshi, T., W.N. Zagotta, and R.W. Aldrich. 1991. Neuron. 7:547–556). Channels were expressed in oocytes and currents were measured with the cut-open-oocyte and patch-clamp techniques. In both clones, the curves describing the voltage dependence of the charge movement were shifted toward more negative potentials when the holding potential was maintained at depolarized potentials. The evidences that this new voltage dependence of the charge movement in the depolarized condition is associated with the process of slow inactivation are the following: (a) the installation of both the slow inactivation of the ionic current and the inactivation of the charge in response to a sustained 1-min depolarization to 0 mV followed the same time course; and (b) the recovery from inactivation of both ionic and gating currents (induced by repolarizations to −90 mV after a 1-min inactivating pulse at 0 mV) also followed a similar time course. Although prolonged depolarizations induce inactivation of the majority of the channels, a small fraction remains non–slow inactivated. The voltage dependence of this fraction of channels remained unaltered, suggesting that their activation pathway was unmodified by prolonged depolarization. The data could be fitted to a sequential model for Shaker K+ channels (Bezanilla, F., E. Perozo, and E. Stefani. 1994. Biophys. J. 66:1011–1021), with the addition of a series of parallel nonconducting (inactivated) states that become populated during prolonged depolarization. The data suggest that prolonged depolarization modifies the conformation of the voltage sensor and that this change can be associated with the process of slow inactivation.
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1 November 1997
Article|
November 01 1997
Correlation between Charge Movement and Ionic Current during Slow Inactivation in Shaker K+ Channels
Riccardo Olcese,
Riccardo Olcese
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
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Ramón Latorre,
Ramón Latorre
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
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Ligia Toro,
Ligia Toro
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
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Francisco Bezanilla,
Francisco Bezanilla
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
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Enrico Stefani
Enrico Stefani
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
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Riccardo Olcese
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
Ramón Latorre
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
Ligia Toro
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
Francisco Bezanilla
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
Enrico Stefani
From the *Department of Anesthesiology, ‡Department of Physiology, §Department of Molecular and Medical Pharmacology, and ‖Brain Research Institute, University of California, Los Angeles, CA 90095-1778; ¶Centro de Estudios Cientificos de Santiago, and Department of Biology, Faculty of Science, University of Chile, Santiago, 9 Chile; and **Conicet, Buenos Aires, 1033 Argentina
Address correspondence to Dr. Enrico Stefani, Department of Anesthesiology, BH-612 CHS, Box 951778, University of California, Los Angeles, Los Angeles, CA 90095-1778. Fax: 310-825-6649; E-mail: [email protected]
1
Abbreviations used in this paper: COVG, cut-open oocyte Vaseline gap voltage clamp; G-V, conductance–voltage; HP, holding potential; MES, methanesulphonic acid; NMG-MES, N-methylglucamine-MES.
Received:
June 26 1997
Accepted:
August 25 1997
Online ISSN: 1540-7748
Print ISSN: 0022-1295
1997
J Gen Physiol (1997) 110 (5): 579–589.
Article history
Received:
June 26 1997
Accepted:
August 25 1997
Citation
Riccardo Olcese, Ramón Latorre, Ligia Toro, Francisco Bezanilla, Enrico Stefani; Correlation between Charge Movement and Ionic Current during Slow Inactivation in Shaker K+ Channels . J Gen Physiol 1 November 1997; 110 (5): 579–589. doi: https://doi.org/10.1085/jgp.110.5.579
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