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Phosphatidylinositol (4,5)-bisphosphate dynamically regulates the K2P background K+ channel TASK-2

机译:磷脂酰肌醇(4,5) - 磷酸磷酸动态调节K2P背景K +通道任务-2

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Two-pore domain K2P K+ channels responsible for the background K+ conductance and the resting membrane potential, are also finely regulated by a variety of chemical, physical and physiological stimuli. Hormones and transmitters acting through Gq protein-coupled receptors (GqPCRs) modulate the activity of various K2P channels but the signalling involved has remained elusive, in particular whether dynamic regulation by membrane PI(4,5)P2, common among other classes of K+ channels, affects K2P channels is controversial. Here we show that K2P K+ channel TASK-2 requires PI(4,5)P2 for activity, a dependence that accounts for its run down in the absence of intracellular ATP and its full recovery by addition of exogenous PI(4,5)P2, its inhibition by low concentrations of polycation PI scavengers, and inhibition by PI(4,5)P2 depletion from the membrane. Comprehensive mutagenesis suggests that PI(4,5)P2 interaction with TASK-2 takes place at C-terminus where three basic aminoacids are identified as being part of a putative binding site.
机译:负责背景K +电导和静止膜电位负责的双孔结构域K2P K +通道也通过各种化学,物理和生理刺激来精细调节。通过GQ蛋白偶联受体(GQPCR)作用的激素和发射器调节各种K2P通道的活性,但是所涉及的信号传导仍然难以捉摸,特别是膜PI(4,5)P2的动态调节,包括在其他类别的K +通道中的常见。 ,影响K2P频道是争议的。在这里,我们表明K2P K +通道任务-2需要PI(4,5)P2进行活性,依赖于在没有细胞内ATP的情况下造成的依赖性及其通过添加外源PI(4,5)P2 ,通过低浓度的络合Pi清除剂抑制,并通过PI(4,5)P2从膜中耗尽的抑制。综合诱变表明,PI(4,5)P2与任务-2的相互作用发生在C末端,其中三个基本氨基酸作为推定结合位点的一部分。

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