Allosteric effects of permeating cations on gating currents during K+ channel deactivation

被引:56
作者
Chen, FSP [1 ]
Steele, D [1 ]
Fedida, D [1 ]
机构
[1] QUEENS UNIV, DEPT PHYSIOL, KINGSTON, ON K7L 3N6, CANADA
关键词
potassium channel; Kv1.5; gating current;
D O I
10.1085/jgp.110.2.87
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
K+ channel gating currents are usually measured ill the absence of permeating ions, when a common feature of channel closing is a rising phase of off-gating current and slow subsequent decay. Current models of gating invoke a concerted rearrangement of subunits just before die open state to explain this very slow charge return from opening potentials. We have measured gating currents from the voltage-gated K+ channel, Kv1.5, highly overexpressed in human embryonic kidney cells. In the presence of permeating K+ or Cs+, we show, by comparison with data obtained in the absence of permeant ions, that there is a rapid return of charge after depolarizations, Measurement of off-gating currents on repolarization before and after K+ dialysis from cells allowed a comparison of off-gating current amplitudes and time course in the same cells. Parallel experiments utilizing the low permeability of Cs+ through Kv1.5 revealed similar rapid charge return during measurements of off-gating currents at E-Cs. Such effects could not be reproduced in a nonconducting mutant (W472F) of Kv1.5, in which, by definition, ion permeation was macroscopically absent. This preservation of a fast kinetic structure of off-gating currents on return from potentials at which channels open suggests an allosteric modulation by permeant cations. This may arise fi om a direct action on a slow step late in the activation pathway, or via a retardation in the rate of C-type inactivation. The activation energy barrier for K+ channel closing is reduced, which may be important during repetitive action potential spiking where ion channels characteristically undergo continuous cyclical activation and deactivation.
引用
收藏
页码:87 / 100
页数:14
相关论文
共 51 条
[21]  
Kirsch Glenn E., 1997, Biophysical Journal, V72, pA232
[22]  
Krovetz H. S., 1997, Biophysical Journal, V72, pA232
[23]   Transmembrane movement of the Shaker K+ channel S4 [J].
Larsson, HP ;
Baker, OS ;
Dhillon, DS ;
Isacoff, EY .
NEURON, 1996, 16 (02) :387-397
[24]   A voltage-dependent role for K+ in recovery from C-type inactivation [J].
Levy, DI ;
Deutsch, C .
BIOPHYSICAL JOURNAL, 1996, 71 (06) :3157-3166
[25]   Dynamic rearrangement of the outer mouth of a K+ channel during gating [J].
Liu, Y ;
Jurman, ME ;
Yellen, G .
NEURON, 1996, 16 (04) :859-867
[26]  
LOBODA A, 1997, BIOPHYS J, V72, pA28
[27]  
LOPEZBARNEO J, 1993, RECEPTOR CHANNEL, V1, P61
[28]   MUTATIONS AFFECTING TEA BLOCKADE AND ION PERMEATION IN VOLTAGE-ACTIVATED K+ CHANNELS [J].
MACKINNON, R ;
YELLEN, G .
SCIENCE, 1990, 250 (4978) :276-279
[29]   Direct physical measure of conformational rearrangement underlying potassium channel gating [J].
Mannuzzu, LM ;
Moronne, MM ;
Isacoff, EY .
SCIENCE, 1996, 271 (5246) :213-216
[30]   STATE-DEPENDENT INACTIVATION OF THE KV3 POTASSIUM CHANNEL [J].
MAROM, S ;
LEVITAN, IB .
BIOPHYSICAL JOURNAL, 1994, 67 (02) :579-589