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dc.rights.licenseopenen_US
dc.contributor.authorWANG, Zixin
dc.contributor.authorHENRIQUES, Alexandre
dc.contributor.authorROUVIÈRE, Laura
dc.contributor.authorCALLIZOT, Noelle
dc.contributor.authorTAN, Lin
dc.contributor.authorHOTCHKIN, Michael T
hal.structure.identifierLaboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM]
dc.contributor.authorROSSIGNOL, Rodrigue
dc.contributor.authorMORTENSON, Mark G
dc.contributor.authorDORFMAN, Adam R
dc.contributor.authorHO, Karen S
dc.contributor.authorWANG, Hui
dc.date.accessioned2023-11-28T13:43:11Z
dc.date.available2023-11-28T13:43:11Z
dc.date.issued2023-09-28
dc.identifier.issn1613-6829en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/186201
dc.description.abstractEnBioenergetic deficits are known to be significant contributors to neurodegenerative diseases. Nevertheless, identifying safe and effective means to address intracellular bioenergetic deficits remains a significant challenge. This work provides mechanistic insights into the energy metabolism-regulating function of colloidal Au nanocrystals, referred to as CNM-Au8, that are synthesized electrochemically in the absence of surface-capping organic ligands. When neurons are subjected to excitotoxic stressors or toxic peptides, treatment of neurons with CNM-Au8 results in dose-dependent neuronal survival and neurite network preservation across multiple neuronal subtypes. CNM-Au8 efficiently catalyzes the conversion of an energetic cofactor, nicotinamide adenine dinucleotide hydride (NADH), into its oxidized counterpart (NAD ), which promotes bioenergy production by regulating the intracellular level of adenosine triphosphate. Detailed kinetic measurements reveal that CNM-Au8-catalyzed NADH oxidation obeys Michaelis-Menten kinetics and exhibits pH-dependent kinetic profiles. Photoexcited charge carriers and photothermal effect, which result from optical excitations and decay of the plasmonic electron oscillations or the interband electronic transitions in CNM-Au8, are further harnessed as unique leverages to modulate reaction kinetics. As exemplified by this work, Au nanocrystals with deliberately tailored structures and surfactant-free clean surfaces hold great promise for developing next-generation therapeutic agents for neurodegenerative diseases.
dc.language.isoENen_US
dc.rightsAttribution-NonCommercial 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/us/*
dc.subject.enBioenergy metabolism
dc.subject.enCatalytic therapeutics
dc.subject.enGold nanocrystals
dc.subject.enNanozymes
dc.subject.enNeurodegenerative diseases
dc.subject.enNeuroprotection
dc.title.enA Mechanism Underpinning the Bioenergetic Metabolism-Regulating Function of Gold Nanocatalysts.
dc.title.alternativeSmallen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/smll.202304082en_US
dc.subject.halSciences du Vivant [q-bio]en_US
dc.identifier.pubmed37767608en_US
bordeaux.journalSmallen_US
bordeaux.page2304082en_US
bordeaux.hal.laboratoriesMaladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.identifierhal-04312203
hal.version1
hal.date.transferred2023-11-28T13:43:14Z
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exporttrue
workflow.import.sourcepubmed
dc.rights.ccCC BY-NCen_US
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