Direct binding of beta-arrestins to two distinct intracellular domains of the delta opioid receptor.
beta-Arrestins regulate opioid receptor-mediated signal transduction and play an important role in opiate-induced analgesia and tolerance/dependence. This study was carried out to measure the direct interaction between beta-arrestins and opioid receptor. Immunoprecipitation experiments demonstrated that beta-arrestin 1 physically interacts with delta opioid receptor (DOR) co-expressed in human embryonic kidney 293 ... cells in an agonist-enhanced manner and truncation of the carboxyl terminus of DOR partially impairs the interaction. In vitro data from glutathione-S-transferase pull-down assay showed that the carboxyl terminus (CT) and the third intracellular loop (I3L) of DOR are both capable of and either domain is sufficient for binding to beta-arrestin 1 and 2. Surface plasmon resonance determination further revealed that binding of CT and I3L of DOR to beta-arrestin is additive, suggesting these two domains bind at distinctly different sites on beta-arrestin without considerable spatial hindrance. This study demonstrated for the first time the direct binding of beta-arrestins to the two distinct domains, the carboxyl terminus and the third intracellular loop, of DOR.
Mesh Terms:
Amino Acid Sequence, Arrestins, Binding Sites, Cell Line, Cloning, Molecular, Cytosol, Escherichia coli, Glutathione Transferase, Humans, Kidney, Molecular Sequence Data, Peptide Fragments, Protein Conformation, Receptors, Opioid, delta, Recombinant Proteins, Transfection
Amino Acid Sequence, Arrestins, Binding Sites, Cell Line, Cloning, Molecular, Cytosol, Escherichia coli, Glutathione Transferase, Humans, Kidney, Molecular Sequence Data, Peptide Fragments, Protein Conformation, Receptors, Opioid, delta, Recombinant Proteins, Transfection
J. Neurochem.
Date: Mar. 01, 2001
PubMed ID: 11259507
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