Molecular cloning of a rat κ opioid receptor reveals sequence similarities to the μ and δ opioid receptors
- 1 November 1993
- journal article
- research article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 295 (3), 625-628
- https://doi.org/10.1042/bj2950625
Abstract
By screening a rat brain cDNA library using a cloned mu opioid receptor cDNA as probe, a clone was identified that is very similar to both the mu and delta opioid receptor sequences. Transient expression of this clone in COS-7 cells showed that it encodes a kappa opioid receptor, designated KOR-1, which is capable of high-affinity binding to kappa-selective ligands. Treatment of transfected cell membranes with bremazocine, a kappa-selective agonist, resulted in a 53% decrease in adenylate cyclase activity, indicating that this kappa opioid receptor displays inhibitory coupling to adenylate cyclase. Thus, one member from each of the three opioid receptor types, mu, kappa and delta, has been molecularly cloned. Analysis of sequence similarities among these opioid receptors, as well as between opioid receptors and other G-protein-coupled receptors, revealed regions of sequence conservation that may underlie the ligand-binding and functional specificities of opioid receptors.Keywords
This publication has 18 references indexed in Scilit:
- Cloning and functional comparison of kappa and delta opioid receptors from mouse brain.Proceedings of the National Academy of Sciences, 1993
- Cloning of a Delta Opioid Receptor by Functional ExpressionScience, 1992
- The delta-opioid receptor: isolation of a cDNA by expression cloning and pharmacological characterization.Proceedings of the National Academy of Sciences, 1992
- Rat brain expresses a heterogeneous family of calcium channels.Proceedings of the National Academy of Sciences, 1990
- Molecular Characterization of Opioid ReceptorsAnnual Review of Pharmacology and Toxicology, 1990
- Two adjacent cysteine residues in the C‐terminal cytoplasmic fragment of bovine rhodopsin are palmitylatedFEBS Letters, 1988
- Identification of residues required for ligand binding to the beta-adrenergic receptor.Proceedings of the National Academy of Sciences, 1987
- Beta-adrenergic receptor kinase: identification of a novel protein kinase that phosphorylates the agonist-occupied form of the receptor.Proceedings of the National Academy of Sciences, 1986
- A highly sensitive adenylate cyclase assayAnalytical Biochemistry, 1974
- Relationship between the inhibition constant (KI) and the concentration of inhibitor which causes 50 per cent inhibition (I50) of an enzymatic reactionBiochemical Pharmacology, 1973