A High Affinity, Highly Selective Ligand for the Delta Opioid Receptor: [3H]-[D-Pen2, pCl-Phe4, d-Pen5]enkephalin
Document Type
Article
Language
eng
Format of Original
8 p.
Publication Date
7-1989
Publisher
Elsevier
Source Publication
Life Sciences
Source ISSN
0024-3205
Original Item ID
doi: 10.1016/0024-3205(89)90154-9
Abstract
Binding characteristics of a new, conformationally constrained, halogenated enkephalin analogue, [3H]-[D-penicillamine2, pCl-Phe4, D-penicillamine5]enkephalin ([3H]pCl-DPDPE), were determined using homogenized rat brain tissue. Saturation binding studies at 25°C determined a dissociation constant (Kd) of 328 ± 27 pM and a receptor density (Bmax) of 87.2 ± 4.2 fmol/mg protein. Kinetic studies demonstrated biphasic association for [3H]pCl-DPDPE, with association rate constants of 5.05 × 108 ± 2.5 × 108 and 0.147 ± 108 ± 0.014 × 108 M−1 min−1. Dissociation was monophasic with a dissociation rate constant of 2.96 × 10−3 ± 0.25 × 10−1 min−1. The average Kd values determined by these kinetic studies were 8.4 ± 2.7 pM and 201 ± 4 pM. Competitive inhibition studies demonstrated that [3H]pCl-DPDPE has excellent selectively for the delta opioid receptor. [3H]pCl-DPDPE binding was inhibited by low concentrations of ligands selective for delta opioid receptor relative to the concentrations required by ligands selective for mu and kappa sites. These data show that [3H]pCl-DPDPE is a highly selective, high affinity ligand which should be useful in characterizing the delta opioid receptor.
Recommended Citation
Vaughn, Linda K.; Knapp, Richard J.; Toth, Geza; Wan, Y. P.; Hruby, Victor J.; and Yamamura, Henry I., "A High Affinity, Highly Selective Ligand for the Delta Opioid Receptor: [3H]-[D-Pen2, pCl-Phe4, d-Pen5]enkephalin" (1989). Biomedical Sciences Faculty Research and Publications. 77.
https://epublications.marquette.edu/biomedsci_fac/77
Comments
Life Sciences, Vol. 45, No. 11 (July 1989): 1101-1108. DOI.