首页> 美国卫生研究院文献>Biophysical Journal >Gating and flickery block differentially affected by rubidium in homomeric KCNQ1 and heteromeric KCNQ1/KCNE1 potassium channels.
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Gating and flickery block differentially affected by rubidium in homomeric KCNQ1 and heteromeric KCNQ1/KCNE1 potassium channels.

机译:homo和闪烁的阻滞在同质KCNQ1和异质KCNQ1 / KCNE1钾通道中受by的影响不同。

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摘要

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.
机译:电压门控钾通道KCNQ1与小的KCNE1亚基结合形成心脏IKs延迟的整流钾电流,两个基因的突变均可导致长期QT综合征。 KCNQ1可以形成功能性同四聚体通道,但是与异聚体KCNQ1 / KCNE1通道相比,其生物物理特性截然不同。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id(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rub渗透率较小,但用100 mM substitution取代100 mM钾后,同质KCNQ1通道的向内尾电流增加了约三倍,这表明of对门控有影响。但是,tail电流的动力学和稳态激活曲线在in中仅略有变化。通过非平稳噪声分析估算了负电压下的单通道振幅,发现在5 kHz带宽下测量时,rub对同型通道的影响很小(增加了1.2倍)。在较低的截止频率下过滤数据后,表观的单通道电导降低,这表明“闪烁/块状”过程相对较快。 potassium与钾的相对电导率在较低的截止频率下(在10 Hz时约为两倍)增加,这表明rub的主要作用是降低通道阻塞的可能性,从而导致流入电流增加而门控特性没有较大变化。 rub中异聚KCNQ1 / KCNE1通道的宏观向内尾电流减少了约两倍,并显示出明显的S型时程,其延迟类似于同源KCNQ1的失活过程而发展,并表明存在多个打开状态。在带宽为5 kHz时,hetero的异质单体单通道幅度比钾小约2倍。在较低的截止频率处进行滤波会降低表观的单通道电导,但是rub与钾的电导比与截止频率无关。我们的结果表明存在一个相对较快的过程(闪烁),该过程几乎独立于门控状态而发生。 negative在负电压下的占据有利于闪变开放状态并减慢同源通道中的闪烁速率,而rub不影响异聚通道中的闪烁。 KCNE1对传导特性的影响与通道外前庭中KCNE1的相互作用一致。

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