Complexation of Poly(ethylene glycol)-(ds)OligoDNA Conjugates with Ionic Liquids

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dc.contributor.authorKim, Young Hunko
dc.contributor.authorJeon, Nayeongko
dc.contributor.authorPark, Sujinko
dc.contributor.authorChoi, Siyoung Q.ko
dc.contributor.authorLee, Eunjiko
dc.contributor.authorLi, Shengko
dc.date.accessioned2024-06-19T14:00:20Z-
dc.date.available2024-06-19T14:00:20Z-
dc.date.created2024-06-19-
dc.date.created2024-06-19-
dc.date.created2024-06-19-
dc.date.issued2024-04-
dc.identifier.citationACS Macro Letters, v.13, no.5, pp.528 - 536-
dc.identifier.issn2161-1653-
dc.identifier.urihttp://hdl.handle.net/10203/319878-
dc.description.abstractWe report the complexation of poly(ethylene glycol) conjugated double-stranded oligoDNA (PEG-(ds)oligoDNA) with imidazolium-based ionic liquids (ILs) to form polyelectrolyte complex aggregates (PCAs). The PEG-(ds)oligoDNA conjugates are prepared following a solution-phase coupling reaction. The binding of PEG-(ds)oligoDNA with either 1-butyl-3-methylimidazolium tetrafluoroborate ([BMIM][BF4]) or 1-hexyl-3-methylimidazolium tetrafluoroborate ([HMIM][BF4]) is confirmed by a fluorescence displacement assay. Both ILs show stronger binding affinity to PEG-(ds)oligoDNA than bare (ds)oligoDNA due to the PEG-assisted increase in IL cation concentration in the vicinity of (ds)oligoDNA. The complex morphology formed at various amine (N) to phosphate (P) ratios is also examined. At high N/P ratios above 4, nanosized PCAs are formed, driven by a counterion-mediated attraction among the IL-bound (ds)oligoDNA segments and stabilized by the conjugated PEG segments. The PCAs exhibit near-neutral surface charges and resistance to DNase degradation, suggesting their potential use in gene delivery applications.-
dc.languageEnglish-
dc.publisherAmerican Chemical Society (ACS)-
dc.titleComplexation of Poly(ethylene glycol)-(ds)OligoDNA Conjugates with Ionic Liquids-
dc.typeArticle-
dc.identifier.wosid001204941300001-
dc.identifier.scopusid2-s2.0-85190741043-
dc.type.rimsART-
dc.citation.volume13-
dc.citation.issue5-
dc.citation.beginningpage528-
dc.citation.endingpage536-
dc.citation.publicationnameACS Macro Letters-
dc.identifier.doi10.1021/acsmacrolett.4c00028-
dc.contributor.localauthorChoi, Siyoung Q.-
dc.contributor.localauthorLi, Sheng-
dc.contributor.nonIdAuthorJeon, Nayeong-
dc.contributor.nonIdAuthorLee, Eunji-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusANTISENSE OLIGONUCLEOTIDE-
dc.subject.keywordPlusDELIVERY-SYSTEM-
dc.subject.keywordPlusDNA-
dc.subject.keywordPlusBINDING-
dc.subject.keywordPlusSTABILITY-
dc.subject.keywordPlusMECHANISM-
dc.subject.keywordPlusPRECIPITATION-
dc.subject.keywordPlusNANOPARTICLES-
dc.subject.keywordPlusHYBRIDIZATION-
dc.subject.keywordPlusCOUNTERIONS-
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