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PMID: 9428002 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Phosphorylation of phospholipase C-coupled receptors.

Pharmacology & therapeutics ·Vol. 75 ·No. 2 ·1997-08-00 ·Pages 135-51

Tobin AB

Abstract

Early work on G-protein-coupled receptor (GPCR) phosphorylation focused on the adenylyl cyclase-linked beta-adrenoceptor, where phosphorylation at sites on the C-terminal tail and within the third intracellular loop results in receptor desensitisation. In recent years, intense research activity has revealed that a large number of GPCR subtypes exist as phosphoproteins, where the level of phosphorylation is dramatically increased subsequent to receptor stimulation. Among these receptor subtypes are those receptors coupled to phospholipase C (PLC). It appears, therefore, that regulation via receptor phosphorylation is a mechanism employed by all but a few GPCRs, including those coupled to PLC. Because the majority of GPCRs are coupled to the phosphoinositide signalling pathway, receptor phosphorylation of PLC-coupled receptors is a regulatory process with profound physiological significance for a huge array of biological responses. This review discusses the properties of homologous and heterologous phosphorylation of PLC-coupled receptors, together with the receptor kinases involved and the functional significance of receptor phosphorylation.

MeSH Terms
Animals Cyclic AMP-Dependent Protein Kinases/metabolism GTP-Binding Proteins/metabolism Phosphorylation Protein Kinases/metabolism Receptors, Adrenergic, beta/metabolism Receptors, Cell Surface/metabolism Receptors, G-Protein-Coupled Saccharomyces cerevisiae Proteins Signal Transduction/physiology Type C Phospholipases/metabolism beta-Adrenergic Receptor Kinases
Chemicals
GPR1 protein, S cerevisiae Receptors, Adrenergic, beta Receptors, Cell Surface Receptors, G-Protein-Coupled Saccharomyces cerevisiae Proteins Protein Kinases Cyclic AMP-Dependent Protein Kinases beta-Adrenergic Receptor Kinases Type C Phospholipases GTP-Binding Proteins
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Tobin A B
Department of Cell Physiology and Pharmacology, University of Leicester, United Kingdom.
Article Info
Journal
Pharmacology & therapeutics
Abbr.
Pharmacol Ther
ISSN
0163-7258
Published
1997-08-00
Pages
135-51
Language
English
Region
England
NLM ID
7905840
Subset
IM
Grants
Wellcome Trust · United Kingdom
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