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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  
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LIPID DOMAINS  
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SPHINGOMYELIN  
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SUPPORTED LIPID BILAYERS  
dc.subject.classification
Biofísica  
dc.subject.classification
Ciencias Biológicas  
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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