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dc.contributor.authorSarott, Roman C.
dc.contributor.authorWestphal, Matthias V.
dc.contributor.authorPfaff, Patrick
dc.contributor.authorRomero, Julián 
dc.contributor.authorRuiz de Martín Esteban, Samuel 
dc.date.accessioned2023-12-14T12:54:31Z
dc.date.available2023-12-14T12:54:31Z
dc.date.issued2020
dc.identifier.issn1520-5126spa
dc.identifier.urihttps://hdl.handle.net/10641/3587
dc.description.abstractPharmacological modulation of cannabinoid type 2 receptor (CB2R) holds promise for the treatment of numerous conditions, including inflammatory diseases, autoimmune disorders, pain, and cancer. Despite the significance of this receptor, researchers lack reliable tools to address questions concerning the expression and complex mechanism of CB2R signaling, especially in cell-type and tissue-dependent contexts. Herein, we report for the first time a versatile ligand platform for the modular design of a collection of highly specific CB2R fluorescent probes, used successfully across applications, species, and cell types. These include flow cytometry of endogenously expressing cells, real-time confocal microscopy of mouse splenocytes and human macrophages, as well as FRET-based kinetic and equilibrium binding assays. High CB2R specificity was demonstrated by competition experiments in living cells expressing CB2R at native levels. The probes were effectively applied to FACS analysis of microglial cells derived from a mouse model relevant to Alzheimer’s disease.spa
dc.language.isoengspa
dc.publisherJournal of the American Chemical Societyspa
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectAnalytical apparatusspa
dc.subjectFluorescencespa
dc.subjectKineticsspa
dc.subjectLigandsspa
dc.subjectProbesspa
dc.titleDevelopment of High-Specificity Fluorescent Probes to Enable Cannabinoid Type 2 Receptor Studies in Living Cells.spa
dc.typejournal articlespa
dc.type.hasVersionSMURspa
dc.rights.accessRightsopen accessspa
dc.description.extent2,41 MBspa
dc.identifier.doi10.1021/jacs.0c05587spa
dc.relation.publisherversionhttps://pubs.acs.org/doi/pdf/10.1021/jacs.0c05587spa


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