Xenopus oocyte electrophysiology in GPCR drug discovery

Publikation: Bidrag til bog/antologi/rapportBidrag til bog/antologiForskning

Deorphanization of the large group of G protein-coupled receptors (GPCRs) for which an endogenous activating ligand has not yet been identified (orphan GPCRs) has become increasingly difficult. A specialized technique that has been successfully applied to deorphanize some of these GPCRs involves two-electrode voltage-clamp recordings of currents through ion channels, which are activated by GPCRs heterologously expressed in Xenopus oocytes. The ion channels that couple to GPCR activation in Xenopus oocytes can be endogenous calcium-activated chloride channels (CaCCs) or heterologously expressed G protein-coupled inwardly rectifying potassium channels (GIRKs). We will describe a general approach for expression of GPCRs in Xenopus oocytes and characterization of these using electrophysiological recordings. We will focus on the detection of GPCR activation by recordings of currents through CaCCs that are activated by calcium release from the endoplasmic reticulum and thus the G(q) signaling pathway.
OriginalsprogEngelsk
TitelG protein-coupled receptors in drug discovery
RedaktørerWayne R Leifert
Vol/bind552
UdgivelsesstedUnited States
ForlagHumana Press
Publikationsdato2009
Sider343-357
ISBN (Trykt)978-1-60327-316-9
ISBN (Elektronisk)978-1-60327-317-6
DOI
StatusUdgivet - 2009
NavnMethods in Molecular Biology
Vol/bind552
ISSN1064-3745

ID: 13063250