Modulation of 5-HT1A receptor signalling by point-mutation of cysteine351 in the rat Gαo protein
- 31 July 1999
- journal article
- Published by Elsevier in Neuropharmacology
- Vol. 38 (7), 1035-1041
- https://doi.org/10.1016/s0028-3908(99)00033-7
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Hydrophobicity of Residue351 of the G Protein Gi1α Determines the Extent of Activation by the α2A-AdrenoceptorBiochemistry, 1998
- Reconstitution of β2‐adrenoceptor−GTP‐binding‐protein interaction in Sf9 cellsEuropean Journal of Biochemistry, 1998
- The structure and signalling properties of 5-HT receptors: an endless diversity?Trends in Pharmacological Sciences, 1998
- Characterisation of a cloned human 5-HT1A receptor cell line using [35S]GTPγS bindingEuropean Journal of Pharmacology, 1997
- Inhibition of the constitutive activity of human 5‐HT1A receptors by the inverse agonist, spiperone but not the neutral antagonist, WAY 100,635British Journal of Pharmacology, 1997
- Differences in G-protein activation by μ- and δ-opioid, and cannabinoid, receptors in rat striatumEuropean Journal of Pharmacology, 1996
- Agonist-receptor efficacy II: agonist trafficking of receptor signalsTrends in Pharmacological Sciences, 1995
- Selective Coupling of Prostaglandin E Receptor EP3D to Gi and Gs through Interaction of α-Carboxylic Acid of Agonist and Arginine Residue of Seventh Transmembrane DomainPublished by Elsevier ,1995
- Selective Activation of Inhibitory G-Protein .alpha.-Subunits by Partial Agonists of the Human 5-HT1A ReceptorBiochemistry, 1994
- A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye bindingAnalytical Biochemistry, 1976