首页> 外文期刊>The Journal of Physiology >Phosphatidylinositol-4,5-bisphosphate (PIP2) regulation of strong inward rectifier Kir2.1 channels: multilevel positive cooperativity.
【24h】

Phosphatidylinositol-4,5-bisphosphate (PIP2) regulation of strong inward rectifier Kir2.1 channels: multilevel positive cooperativity.

机译:强大的内向整流器Kir2.1通道的磷脂酰肌醇-4,5-二磷酸(PIP2)调节:多级正合作性。

获取原文
获取原文并翻译 | 示例
           

摘要

Inwardly rectifying potassium (Kir) channels are gated by the interaction of their cytoplasmic regions with membrane-bound phosphatidylinositol-4,5-bisphosphate (PIP(2)). In the present study, we examined how PIP(2) interaction regulates channel availability and channel openings to various subconductance levels (sublevels) as well as the fully open state in the strong inward rectifier Kir2.1 channel. Various Kir2.1 channel constructs were expressed in Xenopus oocytes and single channel or macroscopic currents were recorded from inside-out patches. The wild-type (WT) channel rarely visited the subconductance levels under control conditions. However, upon reducing Kir2.1 channel interaction with PIP(2) by a variety of interventions, including PIP(2) antibodies, screening PIP(2) with neomycin, or mutating PIP(2) binding sites (e.g. K188Q), visitation to the sublevels was markedly increased before channels were converted to an unavailable mode in which they did not open. No channel activity was detected in channels with the double mutation K188A/R189A, a mutant which exhibits extremely weak interaction with PIP(2). By linking subunits together in tandem dimers or tetramers containing mixtures of WT and K188A/R189A subunits, we demonstrate that one functional PIP(2)-interacting WT subunit is sufficient to convert channels from the unavailable to the available mode with a high open probability dominated by the fully open state, with similar kinetics as tetrameric WT channels. Occasional openings to sublevels become progressively less frequent as the number of WT subunits increases. Quantitative analysis reveals that the interaction of PIP(2) with WT subunits exerts strong positive cooperativity in both converting the channels from the unavailable to the available mode, and in promoting the fully open state over sublevels. We conclude that the interaction of PIP(2) with only one Kir2.1 subunit is sufficient for the channel to become available and to open to its full conductance state. Interaction with additional subunits exerts positive cooperativity at multiple levels to further enhance channel availability and promote the fully open state.
机译:向内整流钾(Kir)通道通过其胞质区域与膜结合磷脂酰肌醇-4,5-双磷酸酯(PIP(2))的相互作用来控制。在本研究中,我们研究了PIP(2)相互作用如何将通道可用性和通道开口调节到各种亚电导水平(sublevels)以及强向内整流器Kir2.1通道中的完全打开状态。在非洲爪蟾卵母细胞中表达了各种Kir2.1通道构建体,并记录了由内而外的斑块的单通道或宏观电流。在控制条件下,野生型(WT)通道很少访问子传导水平。但是,在通过多种干预措施(包括PIP(2)抗体),用新霉素筛选PIP(2)或突变PIP(2)结合位点(例如K188Q)来减少Kir2.1通道与PIP(2)的相互作用之后,在将通道转换为无法打开的不可用模式之前,子级别显着增加。在具有双突变K188A / R189A的通道中未检测到通道活性,该突变体与PIP(2)的相互作用极弱。通过在包含WT和K188A / R189A亚基混合物的串联二聚体或四聚体中将亚基连接在一起,我们证明了一个与功能性PIP(2)相互作用的WT亚基足以将通道从不可用模式转换为以高开放概率控制的可用模式通过完全打开状态,具有与四聚体WT通道相似的动力学。随着WT亚单位数量的增加,偶尔开放给子等级的机会越来越少。定量分析表明,PIP(2)与WT亚基的相互作用在将通道从不可用模式转换为可用模式以及促进子级别上的完全开放状态方面都发挥了强大的正合作性。我们得出的结论是,只有一个Kir2.1亚基的PIP(2)相互作用足以使通道变为可用并打开其完全电导状态。与其他亚基的相互作用在多个层面上发挥了积极的协同作用,以进一步增强渠道可用性并促进完全开放的状态。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号