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Aspartic Acid Residue D3 Critically Determines Cx50 Gap Junction Channel Transjunctional Voltage-Dependent Gating and Unitary Conductance

机译:天冬氨酸残基D3决定性地确定Cx50间隙连接通道跨结电压依赖性门控和单位电导

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摘要

Previous studies have suggested that the aspartic acid residue (D) at the third position is critical in determining the voltage polarity of fast Vj-gating of Cx50 channels. To test whether another negatively charged residue (a glutamic acid residue, E) could fulfill the role of the D3 residue, we generated the mutant Cx50D3E. Vj-dependent gating properties of this mutant channel were characterized by double-patch-clamp recordings in N2A cells. Macroscopically, the D3E substitution reduced the residual conductance (Gmin) to near zero and outwardly shifted the half-inactivation voltage (V0), which is a result of both a reduced aggregate gating charge (z) and a reduced free-energy difference between the open and closed states. Single Cx50D3E gap junction channels showed reduced unitary conductance (γj) of the main open state, reduced open dwell time at ±40 mV, and absence of a long-lived substate. In contrast, a G8E substitution tested to compare the effects of the E residue at the third and eighth positions did not modify the Vj-dependent gating profile or γj. In summary, this study is the first that we know of to suggest that the D3 residue plays an essential role, in addition to serving as a negative-charge provider, as a critical determinant of the Vj-dependent gating sensitivity, open-closed stability, and unitary conductance of Cx50 gap junction channels.
机译:先前的研究表明,第三位置的天冬氨酸残基(D)对于确定Cx50通道快速Vj门控的电压极性至关重要。为了测试另一个带负电荷的残基(谷氨酸残基,E)是否可以履行D3残基的作用,我们生成了突变体Cx50D3E。该突变通道的Vj依赖性门控特性通过N2A细胞中的双膜钳记录来表征。从宏观上讲,D3E取代将残余电导(Gmin)降低到接近零并向外移动了半灭活电压(V0),这是由于降低了总的门控电荷(z)和减小了两者之间的自由能差打开和关闭状态。单个Cx50D3E间隙连接通道显示出主要打开状态的单位电导(γj)降低,±40 mV的打开停留时间减少,并且没有长寿命的子状态。相反,经测试用于比较E残基在第三和第八位置的影响的G8E取代并未改变Vj依赖的门控图或γj。总而言之,这项研究是我们所知的第一个研究,它表明D3残基除了作为负电荷提供者外,还作为Vj依赖性门控敏感性,开闭稳定性的关键决定因素。 ,以及Cx50间隙连接通道的单位电导。

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