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Mechanosensitive behavior of bacterial cyclic nucleotide gated (bCNG) ion channels: Insights into the mechanism of channel gating in the mechanosensitive channel of small conductance superfamily

机译:细菌环状核苷酸门控(bCNG)离子通道的机械敏感性行为:洞察小电导超家族的机械敏感性通道中的通道门控机制

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We have recently identified and characterized the bacterial cyclic nucleotide gated (bCNG) subfamily of the larger mechanosensitive channel of small conductance (MscS) superfamily of ion channels. The channel domain of bCNG channels exhibits significant sequence homology to the mechanosensitive subfamily of MscS in the regions that have previously been used as a hallmark for channels that gate in response to mechanical stress. However, we have previously demonstrated that three of these channels are unable to rescue Escherichia coli from osmotic downshock. Here, we examine an additional nine bCNG homologues and further demonstrate that the full-length bCNG channels are unable to rescue E. coli from hypoosmotic stress. However, limited mechanosensation is restored upon removal of the cyclic nucleotide binding domain. This indicates that the C-terminal domain of the MscS superfamily can drive channel gating and further highlight the ability of a superfamily of ion channels to be gated by multiple stimuli.
机译:我们最近确定并表征了离子通道小电导(MscS)超家族的较大机械敏感通道的细菌环核苷酸门控(bCNG)亚家族。 bCNG通道的通道结构域与MscS的机械敏感亚科在先前已用作响应机械应力的通道标记的区域中显示出显着的序列同源性。但是,我们之前已经证明,这些通道中的三个无法从渗透性向下冲击中拯救大肠杆菌。在这里,我们检查了另外9个bCNG同源物,并进一步证明了全长bCNG通道无法从低渗胁迫中拯救大肠杆菌。但是,去除环核苷酸结合结构域后,有限的机械感觉恢复。这表明MscS超家族的C末端结构域可以驱动通道门控,并进一步突出了离子通道超家族被多种刺激控制的能力。

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