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dc.contributor.authorKroksveen, Ann Cathrineen_US
dc.contributor.authorGuldbrandsen, Astriden_US
dc.contributor.authorVaudel, Marcen_US
dc.contributor.authorLereim, Ragnhild Reehorsten_US
dc.contributor.authorBarsnes, Haralden_US
dc.contributor.authorMyhr, Kjell-Mortenen_US
dc.contributor.authorTorkildsen, Øivinden_US
dc.contributor.authorBerven, Frodeen_US
dc.date.accessioned2020-07-03T12:34:25Z
dc.date.available2020-07-03T12:34:25Z
dc.date.issued2017
dc.PublishedKroksveen AC, Guldbrandsen A, Vaudel M, Lereim RR, Barsnes H, Myhr KM, Torkildsen Ø, Berven F. In-depth cerebrospinal fluid quantitative proteome and deglycoproteome analysis: presenting a comprehensive picture of pathways and processes affected by multiple sclerosis. Journal of Proteome Research. 2017;16(1):179-194eng
dc.identifier.issn1535-3907
dc.identifier.issn1535-3893
dc.identifier.urihttps://hdl.handle.net/1956/23324
dc.description.abstractIn the current study, we conducted a quantitative in-depth proteome and deglycoproteome analysis of cerebrospinal fluid (CSF) from relapsing-remitting multiple sclerosis (RRMS) and neurological controls using mass spectrometry and pathway analysis. More than 2000 proteins and 1700 deglycopeptides were quantified, with 484 proteins and 180 deglycopeptides significantly changed between pools of RRMS and pools of controls. Approximately 300 of the significantly changed proteins were assigned to various biological processes including inflammation, extracellular matrix organization, cell adhesion, immune response, and neuron development. Ninety-six significantly changed deglycopeptides mapped to proteins that were not found changed in the global protein study. In addition, four mapped to the proteins oligo-myelin glycoprotein and noelin, which were found oppositely changed in the global study. Both are ligands to the nogo receptor, and the glycosylation of these proteins appears to be affected by RRMS. Our study gives the most extensive overview of the RRMS affected processes observed from the CSF proteome to date, and the list of differential proteins will have great value for selection of biomarker candidates for further verification.en_US
dc.language.isoengeng
dc.publisherACSeng
dc.titleIn-depth cerebrospinal fluid quantitative proteome and deglycoproteome analysis: presenting a comprehensive picture of pathways and processes affected by multiple sclerosisen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2019-11-11T14:27:05Z
dc.description.versionacceptedVersionen_US
dc.rights.holderCopyright 2016 American Chemical Society
dc.identifier.doihttps://doi.org/10.1021/acs.jproteome.6b00659
dc.identifier.cristin1430921
dc.source.journalJournal of Proteome Research
dc.relation.projectBergens forskningsstiftelse: BFS2016REK02
dc.relation.projectNorges forskningsråd: 251235


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