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Keywords: opioid
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Articles

CXCR2 chemokine receptor antagonism enhances DOP opioid receptor function via allosteric regulation of the CXCR2–DOP receptor heterodimer

Geraldine Parenty, Shirley Appelbe, Graeme Milligan
Journal: Biochemical Journal
Biochem J (2008) 412 (2): 245–256.
https://doi.org/10.1042/BJ20071689
Published: 14 May 2008
...Geraldine Parenty; Shirley Appelbe; Graeme Milligan Opioid agonists have a broad range of effects on cells of the immune system, including modulation of the inflammatory response, and opioid and chemokine receptors are co-expressed by many white cells. Hetero-oligomerization of the human DOP opioid...
View article titled, CXCR2 chemokine receptor antagonism enhances DOP <span class="search-highlight">opioid</span> receptor function via allosteric regulation of the CXCR2–DOP receptor heterodimer
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Articles

Homo- and hetero-oligomeric interactions between G-protein-coupled receptors in living cells monitored by two variants of bioluminescence resonance energy transfer (BRET): hetero-oligomers between receptor subtypes form more efficiently than between less closely related sequences

Douglas RAMSAY, Elaine KELLETT, Mary McVEY, Stephen REES, Graeme MILLIGAN
Journal: Biochemical Journal
Biochem J (2002) 365 (2): 429–440.
https://doi.org/10.1042/bj20020251
Published: 15 July 2002
... separation of the emission spectra of the donor and acceptor moieties compared with traditional BRET. Previously recorded homo-oligomerization of the human δ-opioid receptor was confirmed using BRET 2 . Homo-oligomerization of the κ-opioid receptor was observed using both BRET techniques. Both homo...
View article titled, Homo- and hetero-oligomeric interactions between G-protein-coupled receptors in living cells monitored by two variants of bioluminescence resonance energy transfer (BRET): hetero-oligomers between receptor subtypes form more efficiently than between less closely related sequences
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Articles

Selective inactivation of guanine-nucleotide-binding regulatory protein (G-protein) α and βγ subunits by urea

William K. LIM, Richard R. NEUBIG
Journal: Biochemical Journal
Biochem J (2001) 354 (2): 337–344.
https://doi.org/10.1042/bj3540337
Published: 22 February 2001
...-hydroxytryptamine 1A and µ -opioid) expressed in insect cells and two mammalian cell lines. Thus a selectivity of urea for G-protein α versus βγ subunits is established in both concentration and mechanism. 1 To whom correspondence should be addressed, at the Department of Pharmacology (e-mail Rneubig...
View article titled, Selective inactivation of guanine-nucleotide-binding regulatory protein (G-protein) α and βγ subunits by urea
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