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Glutamate receptor channel kinetics: the effect of glutamate concentration.谷氨酸受体通道动力学:谷氨酸浓度的影响。
Biophys J. 1988 Jan;53(1):39-52. doi: 10.1016/S0006-3495(88)83064-9.
2
Burst kinetics of single calcium-activated potassium channels in cultured rat muscle.培养的大鼠肌肉中单个钙激活钾通道的爆发动力学
J Physiol. 1983 Nov;344:605-23. doi: 10.1113/jphysiol.1983.sp014958.
3
Gating kinetics of Ca2+-activated K+ channels from rat muscle incorporated into planar lipid bilayers. Evidence for two voltage-dependent Ca2+ binding reactions.整合到平面脂质双分子层中的大鼠肌肉钙激活钾通道的门控动力学。两个电压依赖性钙结合反应的证据。
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Estimating kinetic constants from single channel data.从单通道数据估算动力学常数。
Biophys J. 1983 Aug;43(2):207-23. doi: 10.1016/S0006-3495(83)84341-0.
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Relationship between membrane excitability and single channel open-close kinetics.膜兴奋性与单通道开闭动力学之间的关系。
Biophys J. 1983 May;42(2):151-7. doi: 10.1016/S0006-3495(83)84381-1.
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Successive openings of the same acetylcholine receptor channel are correlated in open time.同一乙酰胆碱受体通道的连续开放在开放时间上具有相关性。
Biophys J. 1983 Apr;42(1):109-14. doi: 10.1016/S0006-3495(83)84375-6.
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Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.用于从细胞和无细胞膜片进行高分辨率电流记录的改进膜片钳技术。
Pflugers Arch. 1981 Aug;391(2):85-100. doi: 10.1007/BF00656997.
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Relations between the inactivation of sodium channels and the immobilization of gating charge in frog myelinated nerve.蛙有髓神经中钠通道失活与门控电荷固定之间的关系。
J Physiol. 1980 Feb;299:573-603. doi: 10.1113/jphysiol.1980.sp013143.
9
On the stochastic properties of bursts of single ion channel openings and of clusters of bursts.关于单离子通道开放突发以及突发簇的随机特性。
Philos Trans R Soc Lond B Biol Sci. 1982 Dec 24;300(1098):1-59. doi: 10.1098/rstb.1982.0156.
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On the stochastic properties of single ion channels.关于单离子通道的随机特性。
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相邻区间分析区分了来自大鼠骨骼肌的快速氯离子通道的门控机制。

Adjacent interval analysis distinguishes among gating mechanisms for the fast chloride channel from rat skeletal muscle.

作者信息

Blatz A L, Magleby K L

机构信息

Department of Physiology, University of Texas Southwestern Medical Center, Dallas 75235.

出版信息

J Physiol. 1989 Mar;410:561-85. doi: 10.1113/jphysiol.1989.sp017549.

DOI:10.1113/jphysiol.1989.sp017549
PMID:2477527
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1190495/
Abstract
  1. The durations of adjacent open and shut intervals, obtained with the patch-clamp technique from fast Cl- channels in tissue-cultured rat skeletal muscle, were analysed to distinguish among eight previously considered gating mechanisms for the channel which differed in the connections among the states. 2. Open intervals were separated into groups based on the duration of the shut intervals which occurred before or after each open interval. Fitting these conditional open distributions with sums of exponentials indicated that they were described by two exponential components. 3. The time constants of the two components in the conditional open distributions were independent of the adjacent shut interval durations. The observation of invariant time constants is consistent with gating mechanisms in which the rate constants for transitions among the states remain constant with time (discrete Markov process). 4. In contrast to the invariant time constants, the areas of the two components in the conditional open distributions were dependent on the adjacent shut interval durations. The area of the fast open component increased, and the area of the slow open component decreased, as the duration of adjacent shut intervals increased. Thus, it is changes in areas, rather than time constants, which give rise to the observed inverse relationship between the durations of adjacent open and shut intervals. 5. The findings in summary statements 2-4 indicate that at least two open states are connected by independent pathways to different shut states; the open state associated with the fast open component is connected to a shut state (or compound shut state) of longer effective lifetime, and the open state associated with the slow open component is connected to a shut state (or compound shut state) of briefer effective lifetime. 6. Seven of the eight previously considered gating mechanisms were rejected because they did not account for the observed relationships between the durations of adjacent open and shut intervals, when analysed in terms of either conditional open distributions or conditional mean open interval durations. 7. The seven rejected gating mechanisms also did not account for the observed correlations between interval durations, when analysed in terms of correlation coefficients. Adjacent interval and correlation analysis thus provided a means to distinguish among the gating mechanisms.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 利用膜片钳技术从组织培养的大鼠骨骼肌中的快速氯离子通道获得相邻开放和关闭间隔的持续时间,进行分析以区分先前考虑的八种通道门控机制,这些机制在状态之间的连接上有所不同。2. 根据每个开放间隔之前或之后出现的关闭间隔的持续时间,将开放间隔分组。用指数和拟合这些条件开放分布表明它们由两个指数成分描述。3. 条件开放分布中两个成分的时间常数与相邻关闭间隔的持续时间无关。不变时间常数的观察结果与门控机制一致,即状态之间转换的速率常数随时间保持恒定(离散马尔可夫过程)。4. 与不变时间常数相反,条件开放分布中两个成分的面积取决于相邻关闭间隔的持续时间。随着相邻关闭间隔持续时间的增加,快速开放成分的面积增加,而缓慢开放成分的面积减小。因此,是面积的变化而非时间常数导致了观察到的相邻开放和关闭间隔持续时间之间的反比关系。5. 总结陈述2 - 4中的发现表明,至少两个开放状态通过独立途径连接到不同的关闭状态;与快速开放成分相关的开放状态连接到有效寿命更长的关闭状态(或复合关闭状态),与缓慢开放成分相关的开放状态连接到有效寿命更短的关闭状态(或复合关闭状态)。6. 先前考虑的八种门控机制中的七种被排除,因为当根据条件开放分布或条件平均开放间隔持续时间进行分析时,它们无法解释观察到的相邻开放和关闭间隔持续时间之间的关系。7. 当根据相关系数进行分析时,这七种被排除的门控机制也无法解释观察到的间隔持续时间之间的相关性。相邻间隔和相关性分析因此提供了一种区分门控机制的方法。(摘要截断于400字)