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Graeme Milligan

Researcher at University of Glasgow

Publications -  570
Citations -  32250

Graeme Milligan is an academic researcher from University of Glasgow. The author has contributed to research in topics: Receptor & G protein. The author has an hindex of 88, co-authored 556 publications receiving 30032 citations. Previous affiliations of Graeme Milligan include University of Leicester & Autonomous University of Barcelona.

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Agonist regulation of adenylate cyclase activity in neuroblastoma x glioma hybrid NG108-15 cells transfected to co-express adenylate cyclase type II and the beta 2-adrenoceptor. Evidence that adenylate cyclase is the limiting component for receptor-mediated stimulation of adenylate cyclase activity.

TL;DR: It is demonstrated that the maximal output of the stimulatory arm of theAdenylate cyclase cascade can be increased by increasing total levels of adenylates cyclase in the genetic background of NG108-15 cells.
Journal Article

Thyrotropin-releasing hormone-induced subcellular redistribution and down-regulation of G11alpha: analysis of agonist regulation of coexpressed G11alpha species variants.

TL;DR: Using this system, both agonist-induced subcellular redistribution and down-regulation of G11alpha and beta subunit proteins in response to activation of a phospholipase C coupled receptor are demonstrated.
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G Protein-Coupled Receptor Fusion Proteins in Drug Discovery

TL;DR: Introduction of N-terminal tags to receptors has also allowed the introduction of novel assay techniques based on a pH-sensitive cyanine dye that have the capacity to overcome certain limitations of GPCR-fluorescent protein fusions.
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The palmitoylation status of the G-protein G(o)1 alpha regulates its activity of interaction with the plasma membrane.

TL;DR: Plasmids containing cDNAs encoding either the wild-type guanine-nucleotide-binding protein G(o)1 alpha or the palmitoylation-negative cysteine-3-to-serine (C3S) mutant of G(i)1alpha were transfected into Rat 1 cells, and clones stably expressing immunoreactivity corresponding to these polypeptides were isolated.