Redox proteomic profiling of neuroketal-adducted proteins in human brain: regional vulnerability at middle age increases in the elderly

dc.contributor.authorDomínguez González, Mayelín
dc.contributor.authorOliveira, Eliandre
dc.contributor.authorOdena Caballol, Antonia
dc.contributor.authorPortero-Otin, Manuel
dc.contributor.authorPamplona, Reinald
dc.contributor.authorFerrer, Isidro (Ferrer Abizanda)
dc.date.accessioned2020-01-23T13:26:28Z
dc.date.available2020-01-23T13:26:28Z
dc.date.issued2016-06-01
dc.date.updated2020-01-23T13:26:28Z
dc.description.abstractProtein lipoxidation was assessed in the parietal cortex (PC), frontal cortex (FC), and cingulate gyrus (CG) in middle-aged and old-aged individuals with no clinical manifestations of cognitive impairment, in order to increase understanding of regional brain vulnerability to oxidative damage during aging. Twenty-five lipoxidized proteins were identified in all the three regions although with regional specificities, by using redox proteomics to detect target proteins of neuroketals (NKT) adduction. The number of cases with NKT-adducted proteins was higher in old-aged individuals but most oxidized proteins were already present in middle-aged individuals. Differences in vulnerability to oxidation were dependent on the sub-cellular localization, secondary structure, and external exposition of certain amino acids. Lipoxidized proteins included those involved in energy metabolism, cytoskeleton, proteostasis, neurotransmission and O2/CO2, and heme metabolism. Total NKT and soluble oligomer levels were estimated employing slot-blot, and these were compared between age groups. Oligomers increased with age in PC and FC; NKT significantly increased with age in FC, whereas total NKT and oligomer levels were not modified in CG, thus highlighting differences in brain regional vulnerability with age. Oligomers significantly correlated with NKT levels in the three cortical regions, suggesting that protein NKT adduction parallels soluble oligomer formation.
dc.format.extent15 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec667092
dc.identifier.issn0891-5849
dc.identifier.pmid26968793
dc.identifier.urihttps://hdl.handle.net/2445/148556
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.freeradbiomed.2016.02.034
dc.relation.ispartofFree Radical Biology and Medicine, 2016, vol. 95, p. 1-15
dc.relation.urihttps://doi.org/10.1016/j.freeradbiomed.2016.02.034
dc.rightscc-by-nc-nd (c) Elsevier B.V., 2016
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.sourceArticles publicats en revistes (Patologia i Terapèutica Experimental)
dc.subject.classificationEnvelliment
dc.subject.classificationGenètica
dc.subject.classificationLípids
dc.subject.classificationPeroxidació
dc.subject.classificationTeixit nerviós
dc.subject.classificationEstrès oxidatiu
dc.subject.otherAging
dc.subject.otherGenetics
dc.subject.otherLipids
dc.subject.otherPeroxidation
dc.subject.otherNerve tissue
dc.subject.otherOxidative stress
dc.titleRedox proteomic profiling of neuroketal-adducted proteins in human brain: regional vulnerability at middle age increases in the elderly
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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