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dc.contributor.authorGonzález García, María del Carmen 
dc.contributor.authorHerrero-Foncubierta, Pilar
dc.contributor.authorGarcía-Fernández, Emilio
dc.contributor.authorOrte Gutiérrez, Ángel 
dc.date.accessioned2021-12-01T11:33:20Z
dc.date.available2021-12-01T11:33:20Z
dc.date.issued2020-11-11
dc.identifier.citationGonzalez-Garcia, M.C.; Herrero-Foncubierta, P.; Garcia-Fernandez, E.; Orte, A. Building Accurate Intracellular Polarity Maps through Multiparametric Microscopy. Methods Protoc. 2020, 3, 78. [https://doi.org/10.3390/mps3040078]es_ES
dc.identifier.urihttp://hdl.handle.net/10481/71843
dc.descriptionM.C.G.-G. thanks MICIU/AEI for a predoctoral fellowship. We thank Juan M. Cuerva and Delia Miguel (University of Granada, Spain) for the synthesis of the acridone dyes, Rafael Salto and Maria D. Giron (University of Granada, Spain) for providing the cultured cells, and Amparo Navarro and Tomas Peña-Ruiz (University of Jaen, Spain) for computational studies of the acridone dyes. M.C.G.-G. thanks MICIU/AEI for a predoctoral fellowship. We thank Juan M. Cuerva and Delia Miguel (University of Granada, Spain) for the synthesis of the acridone dyes, Rafael Salto and Maria D. Giron (University of Granada, Spain) for providing the cultured cells, and Amparo Navarro and Tomas Peña-Ruiz (University of Jaen, Spain) for computational studies of the acridone dyes.es_ES
dc.description.abstractThe precise knowledge of intracellular polarity, a physiological parameter that involves complex and intertwined intracellular mechanisms, may be relevant in the study of important diseases like cancer or Alzheimer's. In this technical note, we illustrate our recently developed, accurate method for obtaining intracellular polarity maps employing potent fluorescence microscopy techniques. Our method is based on the selection of appropriate luminescent probes, in which several emission properties vary with microenvironment polarity, specifically spectral shifts and luminescence lifetime. A multilinear calibration is performed, correlating polarity vs. spectral shift vs. luminescence lifetime, to generate a powerful and error-free 3D space for reliable interpolation of microscopy data. Multidimensional luminescence microscopy is then used to obtain simultaneously spectral shift and luminescence lifetime images, which are then interpolated in the 3D calibration space, resulting in accurate, quantitative polarity maps.es_ES
dc.description.sponsorshipSpanish Ministerio de Ciencia e Innovaciónes_ES
dc.description.sponsorshipAgencia Estatal de Investigación and the European Regional Development Fund CTQ2017-85658-R.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsAtribución 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectBiosensinges_ES
dc.subjectCellular microenvironmentes_ES
dc.subjectFluorescence imaginges_ES
dc.subjectFluorescence Lifetime Imaging Microscopy (FLIM)es_ES
dc.subjectLifetimees_ES
dc.subjectAcridoneses_ES
dc.subjectSolvatochromismes_ES
dc.titleBuilding Accurate Intracellular Polarity Maps through Multiparametric Microscopyes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.3390/mps3040078
dc.type.hasVersionVoRes_ES


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