Regulation of KCNQ channels by manipulation of phosphoinositides

Abstract

Activation of phospholipase C (PLC) through G-protein-coupled receptors produces a large number of second messengers and regulates many physiological processes. Many membrane proteins including ion channels require the phosphoinositide phosphatidylinositol 4,5-bisphosphate (PIP2) to function. Activation of PLC can shut down their activity if it depletes the PIP2 pool strongly. Such a mechanism accounts for the muscarinic suppression of current in KCNQ channels. We describe a variety of methods used to show that these channels require PIP2 and that current in the channels is suppressed when receptor-activated PLC depletes PIP2. The methods include observing translocation of lipid-sensitive protein domains, overexpression of enzymes of phosphoinositide metabolism, engineering these enzymes to move to the plasma membrane in response to a chemical signal, and direct chemical analysis of phospholipids. These approaches are general and can be used to test for PIP2 requirements of other membrane proteins. © 2007 The Authors. Journal compilation © 2007 The Physiological Society.