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A Key Agonist-induced Conformational Change in the Cannabinoid Receptor CB1 is Blocked by the Allosteric Ligand Org 27569

Overview
Journal J Biol Chem
Specialty Biochemistry
Date 2012 Aug 1
PMID 22846992
Citations 30
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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.

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References
1.
Xu F, Wu H, Katritch V, Han G, Jacobson K, Gao Z . Structure of an agonist-bound human A2A adenosine receptor. Science. 2011; 332(6027):322-7. PMC: 3086811. DOI: 10.1126/science.1202793. View

2.
De Lean A, Stadel J, Lefkowitz R . A ternary complex model explains the agonist-specific binding properties of the adenylate cyclase-coupled beta-adrenergic receptor. J Biol Chem. 1980; 255(15):7108-17. View

3.
Devane W, Dysarz 3rd F, Johnson M, Melvin L, Howlett A . Determination and characterization of a cannabinoid receptor in rat brain. Mol Pharmacol. 1988; 34(5):605-13. View

4.
Kimura T, Cheng K, Rice K, Gawrisch K . Location, structure, and dynamics of the synthetic cannabinoid ligand CP-55,940 in lipid bilayers. Biophys J. 2009; 96(12):4916-24. PMC: 2712040. DOI: 10.1016/j.bpj.2009.03.033. View

5.
Salom D, Lodowski D, Stenkamp R, Le Trong I, Golczak M, Jastrzebska B . Crystal structure of a photoactivated deprotonated intermediate of rhodopsin. Proc Natl Acad Sci U S A. 2006; 103(44):16123-8. PMC: 1637547. DOI: 10.1073/pnas.0608022103. View