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Endogenous vs Exogenous Allosteric Modulators in GPCRs: A dispute for shuttling CB(1) among different membrane microenvironments

A Cannabinoid Receptor 1 (CB(1)) binding site for the selective allosteric modulator ORG27569 is here identified through an integrate approach of consensus pocket prediction, mutagenesis studies and Mass Spectrometry. This unprecedented ORG27569 pocket presents the structural features of a Cholester...

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Detalles Bibliográficos
Autores principales: Stornaiuolo, Mariano, Bruno, Agostino, Botta, Lorenzo, Regina, Giuseppe La, Cosconati, Sandro, Silvestri, Romano, Marinelli, Luciana, Novellino, Ettore
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4612305/
https://www.ncbi.nlm.nih.gov/pubmed/26482099
http://dx.doi.org/10.1038/srep15453
Descripción
Sumario:A Cannabinoid Receptor 1 (CB(1)) binding site for the selective allosteric modulator ORG27569 is here identified through an integrate approach of consensus pocket prediction, mutagenesis studies and Mass Spectrometry. This unprecedented ORG27569 pocket presents the structural features of a Cholesterol Consensus Motif, a cholesterol interacting region already found in other GPCRs. ORG27569 and cholesterol affects oppositely CB(1) affinity for orthosteric ligands. Moreover, the rise in cholesterol intracellular level results in CB(1) trafficking to the axonal region of neuronal cells, while, on the contrary, ORG27568 binding induces CB(1) enrichment at the soma. This control of receptor migration among functionally different membrane regions of the cell further contributes to downstream signalling and adds a previously unknown mechanism underpinning CB(1) modulation by ORG27569 , that goes beyond a mere control of receptor affinity for orthosteric ligands.