Mostrar el registro sencillo del ítem
dc.contributor.author
Vazquez, Romina Florencia
dc.contributor.author
Erasmo Ovalle-Garcíac
dc.contributor.author
Armando Antillónc
dc.contributor.author
Iván Ortega-Blake
dc.contributor.author
Bakas, Laura Susana
dc.contributor.author
Carlos Muñoz Garay
dc.contributor.author
Maté, Sabina María
dc.date.available
2022-12-13T15:25:29Z
dc.date.issued
2021-01
dc.identifier.citation
Vazquez, Romina Florencia; Erasmo Ovalle-Garcíac; Armando Antillónc; Iván Ortega-Blake; Bakas, Laura Susana; et al.; Asymmetric bilayers mimicking membrane rafts prepared by lipid exchange: Nanoscale characterization using AFM-Force spectroscopy; Elsevier Science; Biochimica et Biophysica Acta - Biomembranes; 1863; 1; 1-2021; 1-11; 183467
dc.identifier.issn
0005-2736
dc.identifier.uri
http://hdl.handle.net/11336/180985
dc.description.abstract
Sphingolipids-enriched rafts domains are proposed to occur in plasma membranes and to mediate important cellular functions. Notwithstanding, the asymmetric transbilayer distribution of phospholipids that exists in the membrane confers the two leaflets different potentials to form lateral domains as next to no sphingolipids are present in the inner leaflet. How the physical properties of one leaflet can influence the properties of the other and its importance on signal transduction across the membrane are questions still unresolved. In this work, we combined AFM imaging and Force spectroscopy measurements to assess domain formation and to study the nanomechanical properties of asymmetric supported lipid bilayers (SLBs) mimicking membrane rafts. Asymmetric SLBs were formed by incorporating N-palmitoyl-sphingomyelin (16:0SM) into the outer leaflet of preformed 1,2-Dioleoyl-sn-glycero-3-phosphocholine (DOPC)/Cholesterol SLBs through methyl-β-cyclodextrin–mediated lipid exchange. Lipid domains were detected after incorporation of 16:0SM though their phase state varied from gel to liquid ordered (Lo) phase if the procedure was performed at 24 or 37 °C, respectively. When comparing symmetric and asymmetric Lo domains, differences in size and morphology were observed, with asymmetric domains being smaller and more interconnected. Both types of Lo domains showed similar mechanical stability in terms of rupture forces and Young's moduli. Notably, force curves in asymmetric domains presented two rupture events that could be attributed to the sequential rupture of a liquid disordered (Ld) and a Lo phase. Interleaflet coupling in asymmetric Lo domains could also be inferred from those measurements. The experimental approach outlined here would significantly enhance the applicability of membrane models.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Elsevier Science
dc.rights
info:eu-repo/semantics/restrictedAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
ATOMIC FORCE MICROSCOPY
dc.subject
FORCE SPECTROSCOPY
dc.subject
LIPID ASYMMETRY
dc.subject
LIPID DOMAINS
dc.subject
SPHINGOMYELIN
dc.subject
SUPPORTED LIPID BILAYERS
dc.subject.classification
Biofísica
dc.subject.classification
Ciencias Biológicas
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS
dc.title
Asymmetric bilayers mimicking membrane rafts prepared by lipid exchange: Nanoscale characterization using AFM-Force spectroscopy
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2022-09-20T18:48:16Z
dc.journal.volume
1863
dc.journal.number
1
dc.journal.pagination
1-11; 183467
dc.journal.pais
Países Bajos
dc.journal.ciudad
Amsterdam
dc.description.fil
Fil: Vazquez, Romina Florencia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina
dc.description.fil
Fil: Erasmo Ovalle-Garcíac. Universidad Nacional Autónoma de México; México
dc.description.fil
Fil: Armando Antillónc. Universidad Nacional Autónoma de México; México
dc.description.fil
Fil: Iván Ortega-Blake. Universidad Nacional Autónoma de México; México
dc.description.fil
Fil: Bakas, Laura Susana. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Departamento de Ciencias Biológicas. Laboratorio de Investigación de Proteínas Vegetales; Argentina
dc.description.fil
Fil: Carlos Muñoz Garay. Universidad Nacional Autónoma de México; México
dc.description.fil
Fil: Maté, Sabina María. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner". Universidad Nacional de la Plata. Facultad de Ciencias Médicas. Instituto de Investigaciones Bioquímicas de La Plata "Prof. Dr. Rodolfo R. Brenner"; Argentina
dc.journal.title
Biochimica et Biophysica Acta - Biomembranes
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/abs/pii/S0005273620303102?via%3Dihub
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.bbamem.2020.183467
Archivos asociados