Study of rabbit erythrocytes membrane solubilization by sucrose monomyristate using laurdan and phasor analysis
Author
dc.contributor.author
Günther Sapunar, Germán
Author
dc.contributor.author
Herlax, Vanesa
Author
dc.contributor.author
Lillo, M. Pilar
Author
dc.contributor.author
Sandoval Altamirano, Catalina
Author
dc.contributor.author
Belmar, Libnny N.
Author
dc.contributor.author
Sánchez, Susana A.
Admission date
dc.date.accessioned
2018-07-26T21:00:03Z
Available date
dc.date.available
2018-07-26T21:00:03Z
Publication date
dc.date.issued
2018
Cita de ítem
dc.identifier.citation
Colloids and Surfaces B-Biointerfaces Volumen: 161 Páginas: 375-385
es_ES
Identifier
dc.identifier.other
10.1016/j.colsurfb.2017.10.068
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/150362
Abstract
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The 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
Patrocinador
dc.description.sponsorship
Fondecyt
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
UCI