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在蛙卵母细胞中表达的人延迟整流钾通道的门控和电导特性。

Gating and conductance properties of a human delayed rectifier K+ channel expressed in frog oocytes.

作者信息

Benndorf K, Koopmann R, Lorra C, Pongs O

机构信息

Zentrum für Physiologie, Universität zu Köln, Germany.

出版信息

J Physiol. 1994 May 15;477(Pt 1):1-14. doi: 10.1113/jphysiol.1994.sp020166.

Abstract
  1. The human delayed rectifier K+ channel h-DRK1, a homologue to the DRK1 channel in the rat, was expressed in Xenopus oocytes. Single-channel currents were measured in micropatches; macroscopic currents were measured either in macropatches, giant patches, or whole oocytes. 2. Macroscopic currents activated at -20 mV and more positive. The instantaneous current-voltage relationship rectified outwardly to a higher degree than predicted by the Goldman-Hodgkin-Katz equation. 3. With the giant patch technique, ionic and putative on- and off-gating currents were recorded simultaneously. The large ratio of the moved gating charges to the amplitude of the ionic current indicated that less than 1% of the gating channels actually opened. 4. The single-channel conductance between 0 and +80 mV was calculated to be 9.4 pS. The channels opened with sublevels which appeared either independently of the fully open level as separate openings, in conjunction with the opening to and closing from the fully open level, or by starting from and ending at the fully open level. 5. The channels opened with two voltage-independent open time constants in the range 1-10 ms (filter 1 kHz). The burst open probability was fitted monoexponentially with time constants in the range of tens of milliseconds. 6. Assuming a sequential Markovian model with four independent voltage-controlled transitions, fit of the steady-state open probability of macroscopic currents showed two components of activation differing in their half-maximal value. 7. The fit of time courses of cumulative first latency and ensemble-averaged currents in single-channel patches suggested that even a single channel may operate with the two different components of activation. 8. It is concluded that h-DRK1 channels considerably rectify in an outward direction and that an apparently flat voltage dependence of activation may be explained by the overlap of two different components.
摘要
  1. 人类延迟整流钾通道h-DRK1是大鼠DRK1通道的同源物,在非洲爪蟾卵母细胞中表达。在微膜片上测量单通道电流;在巨膜片、大膜片或整个卵母细胞中测量宏观电流。2. 宏观电流在-20 mV及更正电位时激活。瞬时电流-电压关系向外整流的程度高于戈德曼-霍奇金- Katz方程的预测。3. 采用巨膜片技术,同时记录离子电流和假定的开、关闸控电流。移动的闸控电荷与离子电流幅度的大比值表明,实际开放的闸控通道不到1%。4. 计算得出0至+80 mV之间的单通道电导为9.4 pS。通道以亚水平开放,这些亚水平要么独立于完全开放水平作为单独的开放出现,与从完全开放水平的开放和关闭同时出现,要么从完全开放水平开始并结束于完全开放水平。5. 通道以1-10 ms范围内的两个电压无关的开放时间常数开放(滤波1 kHz)。爆发开放概率以几十毫秒范围内的时间常数单指数拟合。6. 假设具有四个独立电压控制转变的连续马尔可夫模型,宏观电流稳态开放概率的拟合显示出两个激活成分,其半最大值不同。7. 单通道膜片中累积首次潜伏期和总体平均电流时间进程的拟合表明,即使是单个通道也可能以两种不同的激活成分运行。8. 得出的结论是,h-DRK1通道在向外方向上有显著整流,激活的明显平坦电压依赖性可能由两种不同成分的重叠来解释。

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