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The potassium channel KAT1 is activated by plant and animal 14-3-3 proteins

机译:钾通道KAT1被动植物14-3-3蛋白激活

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摘要

14-3-3 proteins modulate the plant inward rectifier K+ channel KAT1 heterologously expressed in Xenopus oocytes. Injection of recombinant plant 14-3-3 proteins into oocytes shifted the activation curve of KAT1 by + 11 mV and increased the tau on. KAT1 was also modulated by 14-3-3 proteins of Xenopus oocytes. Titration of the endogenous 14-3-3 proteins by injection of the peptide Raf 621p resulted in a strong decrease in KAT1 current (similar to 70% at -150 mV). The mutation K56E performed on plant protein 14-3-3 in a highly conserved recognition site prevented channel activation. Because the maximal conductance of KAT1 was unaffected by 14-3-3, we can exclude that they act by increasing the number of channels, thus ruling out any effect of these proteins on channel trafficking and/or insertion into the oocyte membrane. 14-3-3 proteins also increased KAT1 current in inside-out patches, suggesting a direct interaction with the channel. Direct interaction was confirmed by overlay experiments with radioactive 14-3-3 on oocyte membranes expressing KAT1.
机译:14-3-3蛋白调节在非洲爪蟾卵母细胞中异源表达的植物内向整流子K +通道KAT1。将重组植物14-3-3蛋白注入卵母细胞会使KAT1的激活曲线偏移+ 11 mV,并增加tau值。爪蟾卵母细胞的14-3-3蛋白也调节KAT1。通过注射Raf 621p肽滴定内源性14-3-3蛋白导致KAT1电流大大降低(在-150 mV时约为70%)。在高度保守的识别位点上对植物蛋白14-3-3进行的突变K56E阻止了通道激活。因为KAT1的最大电导率不受14-3-3的影响,所以我们可以排除它们通过增加通道数量来起作用,从而排除了这些蛋白对通道运输和/或插入卵母细胞膜的任何影响。 14-3-3蛋白还增加了由内而外的补丁中KAT1电流,表明与通道直接相互作用。通过与放射性14-3-3在表达KAT1的卵母细胞膜上进行的覆盖实验证实了直接相互作用。

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