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Updated: Sep 29, 2026

A Kinetic Fluorescence-based Ca2+ Mobilization Assay to Identify G Protein-coupled Receptor Agonists, Antagonists, and Allosteric Modulators
Published on: February 20, 2018
Heterotrimeric G proteins control diverse pathways of transmembrane signaling, a base for drug discovery
1Laboratoire de Neuroimmunopharmacologie, INSERM U425, Faculté de Pharmacie, Université Louis Pasteur - Strasbourg 1, BP24, 67401 Illkirch Cedex, France. landry@pharma.u-strasbg.fr
Abstract:
Heptahelical receptors are coupled to heterotrimeric GTP-binding proteins (G proteins) which transduce most signals through their alpha and betagamma subunits to effectors including adenylylcyclases, ion channels, phospholipases Cbeta, and phosphoinositide 3-kinases. The diversity of G proteins, their effectors and regulators (RGS proteins), supports the interest of these protein families as potential drug targets.
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