| Literature DB >> 8001688 |
T Onogi1, M Minami, Y Katao, T Nakagawa, Y Aoki, T Toya, S Katsumata, M Satoh.
Abstract
The structural basis of mu-opioid receptor (OPR) for the specificity in its ligand binding was investigated using chimeric mu/delta-OPRs. Replacement of the region around the first extracellular loop of delta-OPR with the corresponding region of mu-OPR gave the resultant chimeric receptor the similar affinity to DAMGO compared with the native mu-OPR. The reciprocal replacement deprived the high affinity to DAMGO from mu-OPR. These results indicate that the difference(s) in the structure around the first extracellular loop is critical for DAMGO to distinguish between mu- and delta-OPRs. Furthermore, displacement studies revealed that this region is partly involved in the discrimination between mu- and delta-OPRs by other peptidic mu-selective ligands, such as dermorphin, morphiceptin and CTOP, but not by non-peptidic ligands, such as morphine and naloxone.Entities:
Mesh:
Substances:
Year: 1995 PMID: 8001688 DOI: 10.1016/0014-5793(94)01341-w
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124