Switching agonist/antagonist properties of opiate alkaloids at the delta opioid receptor using mutations based on the structure of the orphanin FQ receptor
F. Meng et al., Switching agonist/antagonist properties of opiate alkaloids at the delta opioid receptor using mutations based on the structure of the orphanin FQ receptor, J BIOL CHEM, 275(29), 2000, pp. 21939-21945
In an earlier study, we have demonstrated that by mutating five amino acid
residues to those conserved in the opioid receptors, the OFQ receptor could
be converted to a functional receptor that bound many opioid alkaloids wit
h nanomolar affinities. Surprisingly, when the reciprocal mutations, Lys-21
4 --> Ala (TM5), Ile-277 --> Val/His-278 --> Gln/Ile-279 --> Val (TM6), and
Ile-304 --> Thr (TM7), are introduced in the 6 receptor, neither the indiv
idual mutations nor their various combinations significantly reduce the bin
ding affinities of opioid alkaloids tested. However, these mutations cause
profound alterations in the functional characteristics of the mutant recept
ors as measured in guanosine 5'-3-O-(thio)triphosphate binding assays, Some
agonists become antagonists at some constructs as they lose their ability
to activate them. Some alkaloid antagonists are transformed into agonists a
t other constructs, but their agonistic effects can still be blocked by the
peptide antagonist TIPP, Even the 6 inverse agonist 7-benzylidenenaltrexon
e becomes an agonist at the mutant containing both the Ile-277 --> Val/His-
278 --> Gln/Ile-279 --> Val and Ile-304 --> Thr mutations. Thus, although t
he mutated residues are thought to be part of the binding pocket, they are
critically involved in the control of the 6 receptor activation process. Th
ese findings shed light on some of the structural bases of ligand efficacy.
They are also compatible with the hypothesis that a ligand may achieve hig
h affinity binding in several different ways, each having different effects
on receptor activation.