Large-conductance Ca2+-activated K+ channels can be activated by membrane voltage in the absence of Ca2+ binding, indicating that these channels contain an intrinsic voltage sensor. The properties of this voltage sensor and its relationship to channel activation were examined by studying gating charge movement from mSlo Ca2+-activated K+ channels in the virtual absence of Ca2+ (<1 nM). Charge movement was measured in response to voltage steps or sinusoidal voltage commands. The charge–voltage relationship (Q–V) is shallower and shifted to more negative voltages than the voltage-dependent open probability (G–V). Both ON and OFF gating currents evoked by brief (0.5-ms) voltage pulses appear to decay rapidly (τON = 60 μs at +200 mV, τOFF = 16 μs at −80 mV). However, QOFF increases slowly with pulse duration, indicating that a large fraction of ON charge develops with a time course comparable to that of IK activation. The slow onset of this gating charge prevents its detection as a component of IgON, although it represents ∼40% of the total charge moved at +140 mV. The decay of IgOFF is slowed after depolarizations that open mSlo channels. Yet, the majority of open channel charge relaxation is too rapid to be limited by channel closing. These results can be understood in terms of the allosteric voltage-gating scheme developed in the preceding paper (Horrigan, F.T., J. Cui, and R.W. Aldrich. 1999. J. Gen. Physiol. 114:277–304). The model contains five open (O) and five closed (C) states arranged in parallel, and the kinetic and steady-state properties of mSlo gating currents exhibit multiple components associated with C–C, O–O, and C–O transitions.
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1 August 1999
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August 01 1999
Allosteric Voltage Gating of Potassium Channels II : Mslo Channel Gating Charge Movement in the Absence of Ca2+
Frank T. Horrigan,
Frank T. Horrigan
aFrom the Department of Molecular and Cellular Physiology, Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California 94305
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Richard W. Aldrich
Richard W. Aldrich
aFrom the Department of Molecular and Cellular Physiology, Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California 94305
Search for other works by this author on:
Frank T. Horrigan
aFrom the Department of Molecular and Cellular Physiology, Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California 94305
Richard W. Aldrich
aFrom the Department of Molecular and Cellular Physiology, Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, California 94305
1used in this paper: BK channel, large-conductance Ca2+-activated K+ channel; NMDG, N-methyl-d-glucamine; TEA, tetraethylammonium
Received:
March 16 1999
Revision Requested:
June 01 1999
Accepted:
June 07 1999
Online ISSN: 1540-7748
Print ISSN: 0022-1295
© 1999 The Rockefeller University Press
1999
The Rockefeller University Press
J Gen Physiol (1999) 114 (2): 305–336.
Article history
Received:
March 16 1999
Revision Requested:
June 01 1999
Accepted:
June 07 1999
Citation
Frank T. Horrigan, Richard W. Aldrich; Allosteric Voltage Gating of Potassium Channels II : Mslo Channel Gating Charge Movement in the Absence of Ca2+ . J Gen Physiol 1 August 1999; 114 (2): 305–336. doi: https://doi.org/10.1085/jgp.114.2.305
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