Buch, Englisch, 250 Seiten, Format (B × H): 158 mm x 233 mm, Gewicht: 1210 g
Reihe: Methods in Molecular Biology
Methods and Protocols
Buch, Englisch, 250 Seiten, Format (B × H): 158 mm x 233 mm, Gewicht: 1210 g
Reihe: Methods in Molecular Biology
ISBN: 978-1-58829-137-0
Verlag: Humana Press
Since the initial discovery of the G protein-coupled receptor system that regulates cyclicAMP production, the G protein field has rapidly expanded. Cell surface receptors that couple to heterotrimeric G proteins, the G prote- coupled receptors (GPCRs), number in the hundreds and bind to a wide div- sity of ligands including, biogenic amines (e. g., adrenaline), lipid derivatives (e. g., lysophosphatidic acid), peptides (e. g., opioid peptides), proteins (e. g., thyroid-stimulating hormone), and odorants to name a few. The GPCR system is found throughout biology in such simple organisms as yeast and in such more complex organisms as Dictyostelium discoideum (slime mold), Caen- habditis elegans (nematode worm), and of course in humans. GPCRs and their associated G protein systems are the subject of intense academic research and because of their involvement in a human biology and disease, the pharmac- tical industry has large research initiatives dedicated to the study of GPCRs. By some estimates, more than 50% of the pharmaceuticals on the market are targeted at GPCRs. The G protein/G protein-coupled receptor system consists of a receptor (GPCR), a heterotrimeric G protein consisting of ?, ?, and ? subunits, and an effector. G protein effector molecules, such as enzymes or ion channels, respond to acti- tion by the G protein to generate second messengers or changes in membrane potential that lead to alterations in cell physiology.
Zielgruppe
Research
Autoren/Hrsg.
Fachgebiete
Weitere Infos & Material
Purification of G Protein Subunits and G Protein Effectors.- Purification of Recombinant G Protein ? Subunits from Escherichia coli.- Purification of G Protein Subunits from Sf9 Insect Cells Using Hexahistidine-Tagged ? and ?? Subunits.- Expression and Purification of Soluble Adenylyl Cyclase from Escherichia coli.- Purification of Phospholipase C ? and Phospholipase C ? from Sf9 Cells.- Assays for G Protein—Dependent Effector Activation In Vitro.- Assay for G Protein-Dependent Activation of Phospholipase C ? Using Purified Protein Components.- Assays of Recombinant Adenylyl Cyclases Expressed in Sf9 Cells.- Assays For G Protein-Coupled Receptor-Mediated and G Protein Subunit-Mediated Effector Activation in Intact Cells.- Measurement of G Protein-Coupled Receptor-Stimulated Phospholipase D Activity in Intact Cells.- Analysis of G Protein-Mediated Activation of Phospholipase C in Cultured Cells.- Receptor Mechanisms, Activity, and Localization.- Intensive Mutational Analysis of G Protein-Coupled Receptors in Yeast.- Green Fluorescent Protein-Tagged ?-Arrestin Translocation as a Measure of G Protein-Coupled Receptor Activation.- Detection of G Protein-Coupled Receptors by Immunofluorescence Microscopy.- Assay of G Protein-Coupled Receptor Activation of G Proteins in Native Cell Membranes Using [35S]GTP?S Binding.- Analysis of the Coupling of G12/13 to G Protein-Coupled Receptors Using a Luciferase Reporter Assay.- Disruption of Endogenous G Protein-Signaling Systems to Understand the Role of G Protein Subunits in Intact Systems.- Selective Inhibition of G Protein-Mediated Pathways Using RGS Domains.- Ribozymes as Tools for Suppression of G Protein ? Subunits.- In Vivo Adenoviral-Mediated Gene Transfer of the ?ARKct to Study the Role of G?? in ArterialRestenosis.- Posttranslational Modifications of Regulators of G Protein Signaling.- Analysis of RGS Protein Palmitoylation.- Methods for Measuring RGS Protein Phosphorylation by G Protein-Regulated Kinases.- Use of Gfp-Tagged G Proteins and Effectors in Intact Cells.- The Use of Green Fluorescent Proteins to View Association Between Phospholipase C? and G Protein Subunits in Cells.- Cellular Localization of GFP-Tagged ? Subunits.
