RT Journal Article
SR Electronic
T1 Antagonist Efficacy in MORS196L Mutant Is Affected by the Interaction between Transmembrane Domains of the Opioid Receptor
JF Journal of Pharmacology and Experimental Therapeutics
JO J Pharmacol Exp Ther
FD American Society for Pharmacology and Experimental Therapeutics
SP 216
OP 226
DO 10.1124/jpet.104.076505
VO 313
IS 1
A1 Patricia A. Claude-Geppert
A1 Jiahui Liu
A1 Jonathan Solberg
A1 Laurie J. Erickson-Herbrandson
A1 Horace H. Loh
A1 Ping-Yee Law
YR 2005
UL http://jpet.aspetjournals.org/content/313/1/216.abstract
AB In a previous study, we demonstrated that antagonists such as naloxone or naltrexone acted as full agonists at the μ-opioid receptor (MOR)/δ-opioid receptor (DOR) chimeric receptor (μδ2, where the DOR sequence from the first extracellular loop to the carboxyl terminus was spliced to the MOR sequence) when a conserved serine residue in transmembrane 4 (TM4) was mutated to leucine. However, when Ser196 in the TM4 of MOR was mutated to Leu, antagonists exhibited partial agonistic properties. Since molecular modeling studies suggested transmembrane movement during receptor activation, the observed partial agonistic properties could be due to TM1 and TM7 interaction. Hence, MOR/DOR chimeric mutant receptors with the MOR TM1 and TM7 sequence (μδ2μ7S196L) or with the MOR TM1 and TM6/7 sequence (μδ2μ67S196L) were constructed to test such a hypothesis. Using four tests of opioid receptor activation, we found that the opioid antagonists were full agonists in chimeric mutant receptor if the TM1 and TM7 were from different opioid receptors. Additionally, when two of the TM7 amino acid residues of MORS196L receptor mutants were mutated (T327A and C330S), resulting in a mutant receptor with DOR TM7 sequence, opioid antagonist naloxone exhibited full agonistic properties. These data suggest that the efficacy of opioid antagonists in the Ser196 mutant can be affected by the interaction between TM1 and TM7. The American Society for Pharmacology and Experimental Therapeutics