A trapped intracellular cation modulates K+ channel recovery from slow inactivation

被引:19
|
作者
Ray, Evan C. [1 ]
Deutsch, Carol [1 ]
机构
[1] Univ Penn, Dept Physiol, Philadelphia, PA 19104 USA
来源
JOURNAL OF GENERAL PHYSIOLOGY | 2006年 / 128卷 / 02期
关键词
D O I
10.1085/jgp.200609561
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Upon depolarization, many voltage-gated potassium channels undergo a time-dependent decrease in conductance known as inactivation. Both entry of channels into an inactivated state and recovery from this state govern cellular excitability. In this study, we show that recovery from slow inactivation is regulated by intracellular permeant cations. When inactivated channels are hyperpolarized, closure of the activation gate traps a cation between the activation and inactivation gates. The identity of the trapped cation determines the rate of recovery, and the ability of cations to promote recovery follows the rank order K+ > NH4+ > Rb+ > Cs+ >> Na+, TMA. The striking similarity between this rank order and that for single channel conductance suggests that these two processes share a common feature. We propose that the rate of recovery from slow inactivation is determined by the ability of entrapped cations to move into a binding site in the channel's selectivity filter, and refilling of this site is required for recovery.
引用
收藏
页码:203 / 217
页数:15
相关论文
共 50 条
  • [41] S641 contributes HERG K+ channel inactivation
    Bian, JS
    Cui, J
    Melman, Y
    McDonald, TV
    CELL BIOCHEMISTRY AND BIOPHYSICS, 2004, 41 (01) : 25 - 39
  • [42] PUTATIVE RECEPTOR FOR THE CYTOPLASMIC INACTIVATION GATE IN THE SHAKER K+ CHANNEL
    ISACOFF, EY
    JAN, YN
    JAN, LY
    NATURE, 1991, 353 (6339) : 86 - 90
  • [43] Selective inhibition of HERG K+ channel inactivation by Cd++
    Johnson, JP
    Bennett, PB
    BIOPHYSICAL JOURNAL, 1999, 76 (01) : A71 - A71
  • [44] Metaflumizone inhibits the honeybee NaV1 channel by targeting recovery from slow inactivation
    Gosselin-Badaroudine, Pascal
    Charnet, Pierre
    Collet, Claude
    Chahine, Mohamed
    FEBS LETTERS, 2017, 591 (23) : 3842 - 3849
  • [45] The Eag Domain Regulates Outward Current Density and Recovery from Inactivation of the hERG K+ Channel Through a Non-Covalent Interaction
    Gustina, Ahleah S.
    Trudeau, Matthew C.
    BIOPHYSICAL JOURNAL, 2010, 98 (03) : 119A - 120A
  • [46] Inhibition of the K+ channel Kv1.4 by acidosis: protonation of an extracellular histidine slows the recovery from N-type inactivation
    Claydon, TW
    Boyett, MR
    Sivaprasadarao, A
    Ishii, K
    Owen, JM
    O'Beirne, HA
    Leach, R
    Komukai, K
    Orchard, CH
    JOURNAL OF PHYSIOLOGY-LONDON, 2000, 526 (02): : 253 - 264
  • [47] MEASUREMENTS OF K+ EFFLUX FROM MYOMETRIUM, DURING HYPOXIA AND INTRACELLULAR ACIDIFICATION, AND ALSO DURING APPLICATION OF K+ CHANNEL AGONISTS AND ANTAGONISTS
    HEATON, R
    WRAY, S
    EISNER, D
    JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 1994, 15 (02) : 174 - 175
  • [48] THE INACTIVATION GATE OF THE SHAKER K+ CHANNEL BEHAVES LIKE AN OPEN-CHANNEL BLOCKER
    DEMO, SD
    YELLEN, G
    NEURON, 1991, 7 (05) : 743 - 753
  • [49] Modulation of slow inactivation gating in Kv4.1 K+ channels.
    Beck, EJ
    Covarrubias, M
    BIOPHYSICAL JOURNAL, 1999, 76 (01) : A414 - A414
  • [50] Development of a K+-channel probe and its use for identification of an intracellular plant membrane K+ channel
    Mi, F.
    Berkowitz, G. A.
    Proceedings of the National Academy of Sciences of the United States of America, 92 (08):