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dc.date.accessioned 2020-08-07T17:26:49Z
dc.date.available 2020-08-07T17:26:49Z
dc.date.issued 2017-02
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/101692
dc.description.abstract Sphingomyelins (SM) and phosphatidylcholines (PC) are major lipid classes in the external plasma membrane leaflet of mammalian cells. A preferential interaction between SM and cholesterol (Cho) in both cell and model membranes has been proposed as central for the formation of Cho- and SM-rich domains in membranes. In this context, the relevance of the SM hydrophobic moiety on its interaction with Cho for domain stabilization has been investigated by our group (1-2). We report here on the effects of sphingomyelin structure on the orientational and conformational properties of monolayers of pure lipids and of two ternary lipid mixtures (DOPC/16:0SM/Cho and DOPC/24:1SM/Cho), which are relevant as mammalian cell membrane models. We investigated interchain interactions, hydrogen bonding, conformational and structural properties using in situ polarization modulated infrared reflection absorption spectroscopy (PM-IRRAS). Our results indicate that the particular properties conferred on sphingolipids by unsaturation have profound implications on membrane organization.Finally, we also explored the orientational and conformational changes in lipid monolayers of DOPC/16:0SM/Cho 2:1:1 after the adsorption/insertion of the active toxin HlyA and its unacylated nonhemolytic precursor ProHlyA, so as to complement our knowledge on the action mechanism of both proteins. en
dc.format.extent 82-82 es
dc.language en es
dc.subject Mammalian membranes es
dc.subject PM-IRRAS es
dc.subject Gibbs monolayers es
dc.subject Alfa hemolysin a es
dc.title Orientational Properties of DOPC/SM/Cholesterol Mixtures: A PM-IRRAS Study en
dc.type Articulo es
sedici.identifier.uri https://ri.conicet.gov.ar/11336/64227 es
sedici.identifier.other https://dx.doi.org/10.1016/j.bpj.2016.11.488 es
sedici.identifier.other hdl:11336/64227 es
sedici.identifier.issn 0006-3495 es
sedici.creator.person Maté, Sabina María es
sedici.creator.person Vázquez, Romina Florencia es
sedici.creator.person Pavinatto, Felippe J. es
sedici.creator.person Daza Millone, María Antonieta es
sedici.creator.person Herlax, Vanesa Silvana es
sedici.creator.person Bakás, Laura Susana es
sedici.creator.person Oliveira, Osvaldo N. es
sedici.creator.person Vela, María Elena es
sedici.subject.materias Ciencias Exactas es
sedici.description.fulltext true es
mods.originInfo.place Instituto de Investigaciones Bioquímicas de La Plata es
mods.originInfo.place Comisión de Investigaciones Científicas de la provincia de Buenos Aires es
mods.originInfo.place Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas es
mods.originInfo.place Centro de Investigación de Proteínas Vegetales es
sedici.subtype Comunicacion es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Biophysical Journal es
sedici.relation.journalVolumeAndIssue vol. 112, no. 3, supl. 1 es


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)