A key agonist-induced conformational change in the cannabinoid receptor CB1 is blocked by the allosteric ligand Org 27569

J Biol Chem. 2012 Sep 28;287(40):33873-82. doi: 10.1074/jbc.M112.352328. Epub 2012 Jul 30.

Abstract

Allosteric ligands that modulate how G protein-coupled receptors respond to traditional orthosteric drugs are an exciting and rapidly expanding field of pharmacology. An allosteric ligand for the cannabinoid receptor CB1, Org 27569, exhibits an intriguing effect; it increases agonist binding, yet blocks agonist-induced CB1 signaling. Here we explored the mechanism behind this behavior, using a site-directed fluorescence labeling approach. Our results show that Org 27569 blocks conformational changes in CB1 that accompany G protein binding and/or activation, and thus inhibit formation of a fully active CB1 structure. The underlying mechanism behind this behavior is that simultaneous binding of Org 27569 produces a unique agonist-bound conformation, one that may resemble an intermediate structure formed on the pathway to full receptor activation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Allosteric Site
  • Animals
  • Buffers
  • COS Cells
  • Chlorocebus aethiops
  • Detergents / pharmacology
  • Fluorescent Dyes / pharmacology
  • Humans
  • Indoles / chemistry*
  • Indoles / pharmacology
  • Kinetics
  • Ligands
  • Mutagenesis, Site-Directed
  • Mutation
  • Piperidines / chemistry*
  • Piperidines / pharmacology
  • Protein Binding
  • Protein Conformation
  • Receptor, Cannabinoid, CB1 / antagonists & inhibitors*
  • Receptor, Cannabinoid, CB1 / physiology*
  • Transfection

Substances

  • 5-chloro-3-ethyl-1H-indole-2-carboxylic acid (2-(4-piperidin-1-yl-phenyl)ethyl)amide
  • Buffers
  • Detergents
  • Fluorescent Dyes
  • Indoles
  • Ligands
  • Piperidines
  • Receptor, Cannabinoid, CB1