Hille Bertil, Dickson Eamonn J, Kruse Martin, Vivas Oscar, Suh Byung-Chang
Department of Physiology and Biophysics, University of Washington School of Medicine, Seattle, WA 98195-7290, USA.
Department of Brain Science, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu 711-873, Republic of Korea.
Biochim Biophys Acta. 2015 Jun;1851(6):844-56. doi: 10.1016/j.bbalip.2014.09.010. Epub 2014 Sep 18.
Phosphoinositides serve as signature motifs for different cellular membranes and often are required for the function of membrane proteins. Here, we summarize clear evidence supporting the concept that many ion channels are regulated by membrane phosphoinositides. We describe tools used to test their dependence on phosphoinositides, especially phosphatidylinositol 4,5-bisphosphate, and consider mechanisms and biological meanings of phosphoinositide regulation of ion channels. This lipid regulation can underlie changes of channel activity and electrical excitability in response to receptors. Since different intracellular membranes have different lipid compositions, the activity of ion channels still in transit towards their final destination membrane may be suppressed until they reach an optimal lipid environment. This article is part of a Special Issue entitled Phosphoinositides.
磷酸肌醇作为不同细胞膜的标志性基序,通常是膜蛋白功能所必需的。在这里,我们总结了明确的证据,支持许多离子通道受膜磷酸肌醇调节这一概念。我们描述了用于测试它们对磷酸肌醇(特别是磷脂酰肌醇4,5-二磷酸)依赖性的工具,并探讨了离子通道磷酸肌醇调节的机制和生物学意义。这种脂质调节可能是通道活性和电兴奋性响应受体变化的基础。由于不同的细胞内膜具有不同的脂质组成,仍在向其最终目的地膜转运的离子通道的活性可能会受到抑制,直到它们到达最佳脂质环境。本文是名为“磷酸肌醇”的特刊的一部分。