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磷脂酰肌醇(4,5)-二磷酸 PIP(2)对 Shaker K(+) [更正]通道的双重作用。

Dual effect of phosphatidylinositol (4,5)-bisphosphate PIP(2) on Shaker K(+) [corrected] channels.

机构信息

INSERM, UMR 1087, Nantes, F-44007, France.

出版信息

J Biol Chem. 2012 Oct 19;287(43):36158-67. doi: 10.1074/jbc.M112.382085. Epub 2012 Aug 29.

DOI:10.1074/jbc.M112.382085
PMID:22932893
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3476283/
Abstract

Phosphatidylinositol (4,5)-bisphosphate (PIP(2)) is a phospholipid of the plasma membrane that has been shown to be a key regulator of several ion channels. Functional studies and more recently structural studies of Kir channels have revealed the major impact of PIP(2) on the open state stabilization. A similar effect of PIP(2) on the delayed rectifiers Kv7.1 and Kv11.1, two voltage-gated K(+) channels, has been suggested, but the molecular mechanism remains elusive and nothing is known on PIP(2) effect on other Kv such as those of the Shaker family. By combining giant-patch ionic and gating current recordings in COS-7 cells, and voltage-clamp fluorimetry in Xenopus oocytes, both heterologously expressing the voltage-dependent Shaker channel, we show that PIP(2) exerts 1) a gain-of-function effect on the maximal current amplitude, consistent with a stabilization of the open state and 2) a loss-of-function effect by positive-shifting the activation voltage dependence, most likely through a direct effect on the voltage sensor movement, as illustrated by molecular dynamics simulations.

摘要

磷脂酰肌醇(4,5)-二磷酸(PIP(2))是质膜的一种磷脂,已被证明是几种离子通道的关键调节剂。Kir 通道的功能研究和最近的结构研究揭示了 PIP(2)对开放状态稳定的主要影响。已经提出 PIP(2)对延迟整流器 Kv7.1 和 Kv11.1(两种电压门控 K(+)通道)也有类似的影响,但分子机制仍不清楚,对于 PIP(2)对其他 Kv 通道(如 Shaker 家族的通道)的影响也一无所知。通过在 COS-7 细胞中结合巨膜片钳离子流和门控电流记录,以及在表达电压依赖性 Shaker 通道的非洲爪蟾卵母细胞中进行电压钳荧光法,我们表明 PIP(2) 1) 对最大电流幅度产生功能增益效应,与开放状态的稳定一致,2) 通过正向移动激活电压依赖性产生功能丧失效应,很可能通过对电压传感器运动的直接影响,如分子动力学模拟所示。

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本文引用的文献

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PIP2 controls voltage-sensor movement and pore opening of Kv channels through the S4-S5 linker.PIP2 通过 S4-S5 连接段控制 Kv 通道电压感受器的运动和孔道的开启。
Proc Natl Acad Sci U S A. 2012 Sep 4;109(36):E2399-408. doi: 10.1073/pnas.1207901109. Epub 2012 Aug 13.
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Regulation of voltage-gated potassium channels by PI(4,5)P2.PI(4,5)P2 对电压门控钾通道的调节作用。
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Crystal structure of the mammalian GIRK2 K+ channel and gating regulation by G proteins, PIP2, and sodium.哺乳动物 GIRK2 K+ 通道的晶体结构以及 G 蛋白、PIP2 和钠离子对门控的调节作用。
Cell. 2011 Sep 30;147(1):199-208. doi: 10.1016/j.cell.2011.07.046.
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Structural basis of PIP2 activation of the classical inward rectifier K+ channel Kir2.2.PIP2 激活经典内向整流钾通道 Kir2.2 的结构基础。
Nature. 2011 Aug 28;477(7365):495-8. doi: 10.1038/nature10370.
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The crystal structure of a voltage-gated sodium channel.电压门控钠离子通道的晶体结构。
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Probing the regulation of TASK potassium channels by PI4,5P₂ with switchable phosphoinositide phosphatases.利用可切换的磷酯酰肌醇磷酸酶探测 PI4,5P₂对 TASK 钾通道的调节作用。
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Intermediate states of the Kv1.2 voltage sensor from atomistic molecular dynamics simulations.Kv1.2 电压传感器的原子分子动力学模拟中间态。
Proc Natl Acad Sci U S A. 2011 Apr 12;108(15):6109-14. doi: 10.1073/pnas.1102724108. Epub 2011 Mar 28.
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Molecular mechanism underlying phosphatidylinositol 4,5-bisphosphate-induced inhibition of SpIH channels.磷脂酰肌醇 4,5-二磷酸诱导 SpIH 通道抑制的分子机制。
J Biol Chem. 2011 Apr 29;286(17):15535-42. doi: 10.1074/jbc.M110.214650. Epub 2011 Mar 7.
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Characterization of a binding site for anionic phospholipids on KCNQ1.KCNQ1 上阴离子磷脂结合位点的特征。
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Phosphatidylinositol-4,5-bisphosphate (PIP(2)) stabilizes the open pore conformation of the Kv11.1 (hERG) channel.磷脂酰肌醇-4,5-二磷酸(PIP(2)) 稳定 Kv11.1(hERG)通道的开放孔构象。
Biophys J. 2010 Aug 9;99(4):1110-8. doi: 10.1016/j.bpj.2010.06.013.