Gamper Nikita, Rohacs Tibor
Institute of Membrane and Systems Biology, Faculty of Biological Sciences, University of Leeds, LS2 9JT, Leeds, UK,
Subcell Biochem. 2012;59:289-333. doi: 10.1007/978-94-007-3015-1_10.
Phosphoinositides, especially phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P(2)] are required for the activity of many different ion channels. This chapter will highlight various aspects of this paradigm, by discussing current knowledge on four different ion channel families: inwardly rectifying K(+) (Kir) channels, KCNQ voltage gated K(+) channels, voltage gated Ca(2+) (VGCC) channels and Transient Receptor Potential (TRP) channels. Our main focus is to discuss functional aspects of this regulation, i.e. how changes in the concentration of PtdIns(4,5)P(2) in the plasma membrane upon phospholipase C activation may modulate the activity of ion channels, and what are the major determinants of this regulation. We also discuss how channels act as coincidence detectors sensing phosphoinositide levels and other signalling molecules. We also briefly discuss the available methods to study phosphoinositide regulation of ion channels, and structural aspects of interaction of ion channel proteins with these phospholipids. Finally, in several cases the effect of PtdIns(4,5)P(2) is more complex than a simple dependence of ion channel activity on the lipid, and we will discuss some these complexities.
磷酸肌醇,尤其是磷脂酰肌醇4,5 - 二磷酸[PtdIns(4,5)P₂],是许多不同离子通道活性所必需的。本章将通过讨论关于四个不同离子通道家族的现有知识来突出这一模式的各个方面:内向整流钾通道(Kir通道)、KCNQ电压门控钾通道、电压门控钙通道(VGCC)和瞬时受体电位(TRP)通道。我们主要关注的是讨论这种调节的功能方面,即磷脂酶C激活后质膜中PtdIns(4,5)P₂浓度的变化如何调节离子通道的活性,以及这种调节的主要决定因素是什么。我们还将讨论通道如何作为同时检测磷酸肌醇水平和其他信号分子的传感器。我们还将简要讨论研究离子通道磷酸肌醇调节的可用方法,以及离子通道蛋白与这些磷脂相互作用的结构方面。最后,在某些情况下,PtdIns(4,5)P₂的作用比离子通道活性对脂质的简单依赖更为复杂,我们将讨论其中的一些复杂性。