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Gating Kinetics of the α1i T-Type Calcium Channel

机译:α1iT型钙通道的门控动力学

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The α1I T-type calcium channel inactivates almost 10-fold more slowly than the other family members (α1G and α1H) or most native T-channels. We have examined the underlying mechanisms using whole-cell recordings from rat α1I stably expressed in HEK293 cells. We found several kinetic differences between α1G and α1I, including some properties that at first appear qualitatively different. Notably, α1I tail currents require two or even three exponentials, whereas α1G tails were well described by a single exponential over a wide voltage range. Also, closed-state inactivation is more significant for α1I, even for relatively strong depolarizations. Despite these differences, gating of α1I can be described by the same kinetic scheme used for α1G, where voltage sensor movement is allosterically coupled to inactivation. Nearly all of the rate constants in the model are 5–12-fold slower for α1I, but the microscopic rate for channel closing is fourfold faster. This suggests that T-channels share a common gating mechanism, but with considerable quantitative variability.
机译:与其他家族成员(α1G和α1H)或大多数天然T通道相比,α1IT型钙通道的失活速度几乎快10倍。我们已经使用来自大鼠α1I的全细胞记录在HEK293细胞中稳定表达的机制进行了研究。我们发现了α1G和α1I之间的一些动力学差异,包括一些最初看起来在性质上不同的特性。值得注意的是,α1I尾电流需要两个或什至三个指数,而α1G尾电流在很宽的电压范围内由单个指数很好地描述了。同样,即使对于相对强的去极化,α1I的闭环失活也更为重要。尽管存在这些差异,但可以通过与α1G相同的动力学方案来描述α1I的门控,在该方案中,电压传感器的运动与变态作用是变构偶联的。对于α1I,几乎所有模型中的速率常数都慢5-12倍,但是通道关闭的微观速率快4倍。这表明T通道共享一个通用的门控机制,但是具有相当大的定量变异性。

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