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Authordc.contributor.authorGünther Sapunar, Germán 
Authordc.contributor.authorHerlax, Vanesa 
Authordc.contributor.authorLillo, M. Pilar 
Authordc.contributor.authorSandoval Altamirano, Catalina 
Authordc.contributor.authorBelmar, Libnny N. 
Authordc.contributor.authorSánchez, Susana A. 
Admission datedc.date.accessioned2018-07-26T21:00:03Z
Available datedc.date.available2018-07-26T21:00:03Z
Publication datedc.date.issued2018
Cita de ítemdc.identifier.citationColloids and Surfaces B-Biointerfaces Volumen: 161 Páginas: 375-385es_ES
Identifierdc.identifier.other10.1016/j.colsurfb.2017.10.068
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/150362
Abstractdc.description.abstractThe study of surfactant and bio membranes interaction is particularly complex due to the diversity in lipid composition and the presence of proteins in natural membranes. Even more difficult is the study of this interaction in vivo since cellular damage may complicate the interpretation of the results, therefore for most of the studies in this field either artificial or model systems are used. One of the model system most used to study biomembranes are erythrocytes due to their relatively simple structure (they lack nuclei and organelles having only the plasma membrane), their convenient experimental manipulation and availability. In this context, we used rabbit erythrocytes as a model membrane and Laurdan (6-lauroyl-2-dimethylaminonaphthalene) as the fluorescent probe to study changes promoted in the membrane by the interaction with the sucrose monoester of myristic acid, beta-n-fructofuranosyl-6-O-myristoyl-alpha-D-glucopyranoside (MMS). Surfactant and erythrocytes interaction was studied by measuring hemoglobin release and the changes in water content in the membrane sensed by Laurdan. Using two-photon excitation, three types of measurements were performed: Generalized Polarization (analyzed as average GP values), Fluorescence Lifetime Imaging, FLIM (analyzed using phasor plots) and Spectral imaging (analyzed using spectral phasor). Our data indicate that at sublytical concentration of surfactant (20 mu M MMS), there is a decrease of about 35% in erythrocytes size, without changes in Laurdan lifetime or emission spectra. We also demonstrate that as hemolysis progress, Laurdan lifetime increased due to the decrease in hemoglobin (strong quencher of Laurdan emission) content inside the erythrocytes. Under these conditions, Laurdan spectral phasor analyses can extract the information on the water content in the membrane in the presence of hemoglobin. Our results indicate an increase in membrane fluidity in presence of MMS. (C) 2017 Elsevier B.V. All rights reserved.es_ES
Patrocinadordc.description.sponsorshipFondecyt 1140454 1080412 Beca de Doctorado Conicyt Agencia Nacional de Promocion Cientifica y Tecnologica PICT 2657/2013 Ministerio de Economiia y Competitividad FIS2015-70339-C2-2-R National Institute of General Medical Sciences of the National Institutes of Health 8P41GM103540 UCIes_ES
Lenguagedc.language.isoenes_ES
Publisherdc.publisherElsevier Science BVes_ES
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Sourcedc.sourceColloids and Surfaces B-Biointerfaceses_ES
Keywordsdc.subjectFLIM phasores_ES
Keywordsdc.subjectSpectral phasores_ES
Keywordsdc.subjectLaurdan GPes_ES
Keywordsdc.subjectSolubilizationes_ES
Keywordsdc.subjectSurfactantses_ES
Keywordsdc.subjectSucrose esteres_ES
Keywordsdc.subjectMembrane heterogeneityes_ES
Keywordsdc.subjectMembrane fluidityes_ES
Títulodc.titleStudy of rabbit erythrocytes membrane solubilization by sucrose monomyristate using laurdan and phasor analysises_ES
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorrgfes_ES
Indexationuchile.indexArtículo de publicación ISIes_ES


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile