Effects of hydroxyl group variations on a flavonoid backbone toward modulation of metal-free and metal-induced amyloid-beta aggregation

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dc.contributor.authorLee, Hyuck Jinko
dc.contributor.authorKerr, Richard A.ko
dc.contributor.authorKorshavn, Kyle J.ko
dc.contributor.authorLee, Jeeyeonko
dc.contributor.authorKang, Juhyeko
dc.contributor.authorRamamoorthy, Ayyalusamyko
dc.contributor.authorRuotolo, Brandon T.ko
dc.contributor.authorLim, Mi Heeko
dc.date.accessioned2018-02-21T06:06:15Z-
dc.date.available2018-02-21T06:06:15Z-
dc.date.created2018-02-08-
dc.date.created2018-02-08-
dc.date.created2018-02-08-
dc.date.issued2016-03-
dc.identifier.citationINORGANIC CHEMISTRY FRONTIERS, v.3, no.3, pp.381 - 392-
dc.identifier.issn2052-1553-
dc.identifier.urihttp://hdl.handle.net/10203/240276-
dc.description.abstractAmyloid-beta (A beta) and metal ions are suggested to be involved in the pathogenesis of Alzheimer's disease (AD). Cu(II) and Zn(II) can interact with A beta and facilitate peptide aggregation producing toxic oligomeric peptide species. Additionally, redox-active metal-bound A beta is shown to generate reactive oxygen species (ROS). Although the interaction of metal ions with A beta and the reactivity of metal-associated A beta (metal-A beta) are indicated, the relationship between metal-A beta and AD etiology is still unclear. Some naturally occurring flavonoids capable of redirecting metal-A beta peptides into nontoxic, off-pathway A beta aggregates have been presented as valuable tools for elucidating the role of metal-A beta in AD. The structural moieties of the flavonoids responsible for their reactivity toward metal-A beta are not identified, however. To determine a structure-interaction-reactivity relationship between flavonoids and metal-free A beta or metal-A beta, four flavonoids (morin, quercetin, galangin, and luteolin) were rationally selected based on structural variations (i.e., number and position of hydroxyl groups). These four flavonoids could noticeably modulate metal-A beta aggregation over metal-free analogue to different extents. Moreover, nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry (MS) studies reveal that the direct interactions of the flavonoids with metal-free and/or metal-bound A beta are distinct. Overall, our studies demonstrate that alternation of the hydroxyl groups on the B and C rings of flavonoids (structure) could differentiate their metal/metal-free A beta/metal-A beta interactions (interaction) and subsequently direct their effects on metal-free A beta and metal-A beta aggregation in vitro and A beta-/metal-A beta-triggered toxicity in living cells (reactivity), suggesting a structure-interaction-reactivity relationship.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleEffects of hydroxyl group variations on a flavonoid backbone toward modulation of metal-free and metal-induced amyloid-beta aggregation-
dc.typeArticle-
dc.identifier.wosid000372250200007-
dc.identifier.scopusid2-s2.0-84960441558-
dc.type.rimsART-
dc.citation.volume3-
dc.citation.issue3-
dc.citation.beginningpage381-
dc.citation.endingpage392-
dc.citation.publicationnameINORGANIC CHEMISTRY FRONTIERS-
dc.identifier.doi10.1039/c5qi00219b-
dc.contributor.localauthorLim, Mi Hee-
dc.contributor.nonIdAuthorLee, Hyuck Jin-
dc.contributor.nonIdAuthorKerr, Richard A.-
dc.contributor.nonIdAuthorKorshavn, Kyle J.-
dc.contributor.nonIdAuthorLee, Jeeyeon-
dc.contributor.nonIdAuthorKang, Juhye-
dc.contributor.nonIdAuthorRamamoorthy, Ayyalusamy-
dc.contributor.nonIdAuthorRuotolo, Brandon T.-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusMOBILITY-MASS SPECTROMETRY-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusSMALL MOLECULES-
dc.subject.keywordPlusFIBRIL FORMATION-
dc.subject.keywordPlusREACTIVITY-
dc.subject.keywordPlusCOMPLEXES-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusOXIDATION-
dc.subject.keywordPlusQUERCETIN-
dc.subject.keywordPlusBINDING-
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