dc.creatorSánchez, María Florencia
dc.creatorLevi, Valeria
dc.creatorWeidemann, Thomas
dc.creatorCarrer, Dolores Catalina
dc.date.accessioned2018-06-22T19:55:07Z
dc.date.available2018-06-22T19:55:07Z
dc.date.created2018-06-22T19:55:07Z
dc.date.issued2015-11-30
dc.identifierSánchez, María Florencia; Levi, Valeria; Weidemann, Thomas; Carrer, Dolores Catalina; Agonist mobility on supported lipid bilayers affects Fas mediated death response; Elsevier Science; FEBS Letters; 589; 23; 30-11-2015; 3527-3533
dc.identifier0014-5793
dc.identifierhttp://hdl.handle.net/11336/49749
dc.identifier1873-3468
dc.identifierCONICET Digital
dc.identifierCONICET
dc.description.abstractExtrinsic apoptosis is initiated by recognition and clustering of the single-pass transmembrane proteins Fas ligand and Fas expressed at the surface of closely apposed lymphocytes and target cells, respectively. Since Fas-mediated death response was mainly studied with soluble antibodies, the mobility constraints for receptor activation by a membrane embedded agonist is not well understood. We explored this influence by stimulating apoptosis on functionalized supported lipid bilayers, where we quantified agonist mobility by z-scan fluorescence correlation spectroscopy. Using different lipid compositions, we show that the apoptotic response correlates with increased lateral mobility of the agonist in the lipid bilayer.
dc.languageeng
dc.publisherElsevier Science
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://febs.onlinelibrary.wiley.com/doi/abs/10.1016/j.febslet.2015.10.009
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/j.febslet.2015.10.009
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectApoptosis
dc.subjectFas Receptor
dc.subjectFluorescence Correlation Spectroscopy
dc.subjectFunctionalized Surface
dc.subjectSupported Lipid Bilayer
dc.titleAgonist mobility on supported lipid bilayers affects Fas mediated death response
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


Este ítem pertenece a la siguiente institución