Regulation of KCNQ channels by manipulation of phosphoinositides

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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 (PIP(2)) to function. Activation of PLC can shut down their activity if it depletes the PIP(2) 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 PIP(2) and that current in the channels is suppressed when receptor-activated PLC depletes PIP(2). 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 PIP(2) requirements of other membrane proteins.