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dc.rights.licenseopenen_US
dc.contributor.authorEWALD, M.
dc.contributor.authorHENRY, S.
dc.contributor.authorLAMBERT, E.
dc.contributor.authorFEUILLIE, Cecile
dc.contributor.authorBOBO, C.
dc.contributor.authorCULLIN, Christophe
ORCID: 0000-0003-4110-4677
IDREF: 85920959
dc.contributor.authorLECOMTE, S.
dc.contributor.authorMOLINARI, M.
dc.date.accessioned2019
dc.date.available2019
dc.date.issued2019
dc.identifier.issn2040-3372en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/3843
dc.description.abstractEnDue to an aging population, neurodegenerative diseases have become a major health issue, the most common being Alzheimer's disease. The mechanisms leading to neuronal loss still remain unclear but recent studies suggest that soluble Aβ oligomers have deleterious effects on neuronal membranes. Here, high-speed atomic force microscopy was used to assess the effect of oligomeric species of a variant of Aβ1-42 amyloid peptide on model membranes with various lipid compositions. Results showed that the peptide does not interact with membranes composed of phosphatidylcholine and sphingomyelin. Ganglioside GM1, but not cholesterol, is required for the peptide to interact with the membrane. Interestingly, when they are both present, a fast disruption of the membrane was observed. It suggests that the presence of ganglioside GM1 and cholesterol in membranes promotes the interaction of the oligomeric Aβ1-42 peptide with the membrane. This interaction leads to the membrane's destruction in a few seconds. This study highlights the power of high-speed atomic force microscopy to explore lipid–protein interactions with high spatio-temporal resolution.
dc.language.isoENen_US
dc.title.enHigh speed atomic force microscopy to investigate the interactions between toxic Aβ 1-42 peptides and model membranes in real time: impact of the membrane composition
dc.title.alternativeNanoscaleen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1039/C8NR08714Hen_US
dc.subject.halChimie/Matériauxen_US
bordeaux.journalNanoscaleen_US
bordeaux.page7229-7238en_US
bordeaux.volume11en_US
bordeaux.hal.laboratoriesInstitut de Chimie & de Biologie des Membranes & des Nano-objets (CBMN) - UMR 5248
bordeaux.issue15en_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.identifierhal-03182025
hal.version1
hal.date.transferred2021-03-26T08:55:07Z
hal.exporttrue
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