We previously demonstrated that the outer vestibule of activated Kv2.1 potassium channels can be in one of two conformations, and that K+ occupancy of a specific selectivity filter site determines which conformation the outer vestibule is in. These different outer vestibule conformations result in different sensitivities to internal and external TEA, different inactivation rates, and different macroscopic conductances. The [K+]-dependent switch in outer vestibule conformation is also associated with a change in rate of channel activation. In this paper, we examined the mechanism by which changes in [K+] modulate the rate of channel activation. Elevation of symmetrical [K+] or [Rb+] from 0 to 3 mM doubled the rate of on-gating charge movement (Qon), measured at 0 mV. Cs+ produced an identical effect, but required 40-fold higher concentrations. All three permeant ions occupied the selectivity filter over the 0.03–3 mM range, so simple occupancy of the selectivity filter was not sufficient to produce the change in Qon. However, for each of these permeant ions, the speeding of Qon occurred with the same concentration dependence as the switch between outer vestibule conformations. Neutralization of an amino acid (K356) in the outer vestibule, which abolishes the modulation of channel pharmacology and ionic currents by the K+-dependent reorientation of the outer vestibule, also abolished the K+-dependence of Qon. Together, the data indicate that the K+-dependent reorientation in the outer vestibule was responsible for the change in Qon. Moreover, similar [K+]-dependence and effects of mutagenesis indicate that the K+-dependent change in rate of Qon can account for the modulation of ionic current activation rate. Simple kinetic analysis suggested that K+ reduced an energy barrier for voltage sensor movement. These results provide strong evidence for a direct functional interaction, which is modulated by permeant ions acting at the selectivity filter, between the outer vestibule of the Kv2.1 potassium channel and the voltage sensor.
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1 April 2004
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March 15 2004
Influence of Permeant Ions on Voltage Sensor Function in the Kv2.1 Potassium Channel
Joseph F. Consiglio,
Joseph F. Consiglio
Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT 06269
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Stephen J. Korn
Stephen J. Korn
Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT 06269
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Joseph F. Consiglio
Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT 06269
Stephen J. Korn
Department of Physiology and Neurobiology, University of Connecticut, Storrs, CT 06269
Address correspondence to Stephen Korn, Department of Physiology and Neurobiology, Box U-156, University of Connecticut, 3107 Horsebarn Hill Rd., Storrs, CT 06269. Fax: (860) 486-3303; email: [email protected]
Abbreviation used in this paper: MTSET, [2-(trimethylammonium)ethyl] methanethiosulfonate.
Received:
January 06 2004
Accepted:
February 20 2004
Online ISSN: 1540-7748
Print ISSN: 0022-1295
The Rockefeller University Press
2004
J Gen Physiol (2004) 123 (4): 387–400.
Article history
Received:
January 06 2004
Accepted:
February 20 2004
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Joseph F. Consiglio, Stephen J. Korn; Influence of Permeant Ions on Voltage Sensor Function in the Kv2.1 Potassium Channel . J Gen Physiol 1 April 2004; 123 (4): 387–400. doi: https://doi.org/10.1085/jgp.200308976
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