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在同聚体KCNQ1和异聚体KCNQ1/KCNE1钾通道中,门控和闪烁阻断受铷的影响不同。

Gating and flickery block differentially affected by rubidium in homomeric KCNQ1 and heteromeric KCNQ1/KCNE1 potassium channels.

作者信息

Pusch M, Bertorello L, Conti F

机构信息

Istituto di Cibernetica e Biofisica, Consiglio Nazionale della Ricerche, Via de Marini 6, I-16149 Genova, Italy.

出版信息

Biophys J. 2000 Jan;78(1):211-26. doi: 10.1016/S0006-3495(00)76586-6.

Abstract

The voltage-gated potassium channel KCNQ1 associates with the small KCNE1 subunit to form the cardiac IKs delayed rectifier potassium current and mutations in both genes can lead to the long QT syndrome. KCNQ1 can form functional homotetrameric channels, however with drastically different biophysical properties compared to heteromeric KCNQ1/KCNE1 channels. We analyzed gating and conductance of these channels expressed in Xenopus oocytes using the two-electrode voltage-clamp and the patch-clamp technique and high extracellular potassium (K) and rubidium (Rb) solutions. Inward tail currents of homomeric KCNQ1 channels are increased about threefold upon substitution of 100 mM potassium with 100 mM rubidium despite a smaller rubidium permeability, suggesting an effect of rubidium on gating. However, the kinetics of tail currents and the steady-state activation curve are only slightly changed in rubidium. Single-channel amplitude at negative voltages was estimated by nonstationary noise analysis, and it was found that rubidium has only a small effect on homomeric channels (1.2-fold increase) when measured at a 5-kHz bandwidth. The apparent single-channel conductance was decreased after filtering the data at lower cutoff frequencies indicative of a relatively fast "flickery/block" process. The relative conductance in rubidium compared to potassium increased at lower cutoff frequencies (about twofold at 10 Hz), suggesting that the main effect of rubidium is to decrease the probability of channel blockage leading to an increase of inward currents without large changes in gating properties. Macroscopic inward tail currents of heteromeric KCNQ1/KCNE1 channels in rubidium are reduced by about twofold and show a pronounced sigmoidal time course that develops with a delay similar to the inactivation process of homomeric KCNQ1, and is indicative of the presence of several open states. The single channel amplitude of heteromers is about twofold smaller in rubidium than in potassium at a bandwidth of 5 kHz. Filtering at lower cutoff frequencies reduces the apparent single-channel conductance, the ratio of the conductance in rubidium versus potassium is, however, independent of the cutoff frequency. Our results suggest the presence of a relatively rapid process (flicker) that can occur almost independently of the gating state. Occupancy by rubidium at negative voltages favors the flicker-open state and slows the flickering rate in homomeric channels, whereas rubidium does not affect the flickering in heteromeric channels. The effects of KCNE1 on the conduction properties are consistent with an interaction of KCNE1 in the outer vestibule of the channel.

摘要

电压门控钾通道KCNQ1与小的KCNE1亚基结合形成心脏IKs延迟整流钾电流,这两个基因的突变都可导致长QT综合征。KCNQ1可形成功能性同源四聚体通道,但其生物物理特性与异源KCNQ1/KCNE1通道相比有很大不同。我们使用双电极电压钳和膜片钳技术以及高细胞外钾(K)和铷(Rb)溶液,分析了非洲爪蟾卵母细胞中表达的这些通道的门控和电导。尽管铷的通透性较小,但将100 mM钾替换为100 mM铷后,同源KCNQ1通道的内向尾电流增加了约三倍,这表明铷对门控有影响。然而,尾电流的动力学和稳态激活曲线在铷中仅略有变化。通过非平稳噪声分析估计负电压下的单通道幅度,发现在5 kHz带宽下测量时,铷对同源通道的影响很小(增加1.2倍)。在较低截止频率对数据进行滤波后,表观单通道电导降低,这表明存在一个相对快速的“闪烁/阻断”过程。与钾相比,铷中的相对电导在较低截止频率下增加(在10 Hz时约增加两倍),这表明铷的主要作用是降低通道阻断的概率,从而导致内向电流增加,而门控特性没有大的变化。铷中异源KCNQ1/KCNE1通道的宏观内向尾电流减少约两倍,并呈现出明显的S形时间进程,其发展延迟与同源KCNQ1的失活过程相似,这表明存在几种开放状态。在5 kHz带宽下,异源体的单通道幅度在铷中比在钾中小约两倍。在较低截止频率下进行滤波会降低表观单通道电导,然而,铷与钾中的电导比与截止频率无关。我们的结果表明存在一个相对快速的过程(闪烁),它几乎可以独立于门控状态而发生。负电压下铷的占据有利于闪烁开放状态,并减缓同源通道中的闪烁速率,而铷不影响异源通道中的闪烁。KCNE1对传导特性的影响与KCNE1在通道外前庭的相互作用一致。

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本文引用的文献

1
Single-channel properties of IKs potassium channels.IKs钾通道的单通道特性
J Gen Physiol. 1998 Dec;112(6):665-78. doi: 10.1085/jgp.112.6.665.
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The long QT syndrome.长QT综合征。
Pediatr Rev. 1998 Jul;19(7):232-8. doi: 10.1542/pir.19-7-232.
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Properties and regulation of the minK potassium channel protein.小电导钾通道蛋白的特性与调控
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