INSERM, UMR 1087, Nantes, F-44007, France.
J Biol Chem. 2012 Oct 19;287(43):36158-67. doi: 10.1074/jbc.M112.382085. Epub 2012 Aug 29.
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.
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。