dc.creatorFanani, Maria Laura
dc.creatorDe Tullio, Luisina
dc.creatorHartel, Steffen
dc.creatorJara, Jorge
dc.creatorMaggio, Bruno
dc.date.accessioned2019-03-11T12:56:51Z
dc.date.available2019-03-11T12:56:51Z
dc.date.created2019-03-11T12:56:51Z
dc.date.issued2009
dc.identifierBiophysical Journal, Volumen 96, Issue 1, 2018, Pages 67-76
dc.identifier15420086
dc.identifier00063495
dc.identifier10.1529/biophysj.108.141499
dc.identifierhttps://repositorio.uchile.cl/handle/2250/164679
dc.description.abstractSphingomyelinase (SMase)-induced ceramide (Cer)-enriched domains in a lipid monolayer are shown to result from an out-of-equilibrium situation. This is induced by a change of composition caused by the enzymatic production of Cer in a sphingomyelin (SM) monolayer that leads to a fast SM/Cer demixing into a liquid-condensed (LC), Cer-enriched and a liquid-expanded, SM-enriched phases. The morphological evolution and kinetic dependence of Cer-enriched domains is studied under continuous observation by epifluorescence microscopy. Domain shape annealing is observed from branched to rounded shapes after SMase activity quenching by EDTA, with a decay halftime of ∼10 min. An out-of-equilibrium fast domain growth is not the determinant factor for domain morphology. Domain shape rearrangement in nearly equilibrium conditions result from the counteraction of intradomain dipolar repulsion and line tension, according to McConnell's shape transition theory. Phase separation causes a transient compos
dc.languageen
dc.publisherBiophysical Society
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceBiophysical Journal
dc.subjectBiophysics
dc.titleSphingomyelinase-induced domain shape relaxation driven by out-of-equilibrium changes of composition
dc.typeArtículos de revistas


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