Please use this identifier to cite or link to this item: https://doi.org/10.1093/nar/gky521
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dc.titleThe role of spacer sequence in modulating turn-on fluorescence of DNA-templated silver nanoclusters
dc.contributor.authorAng, YS
dc.contributor.authorWoon, WWE
dc.contributor.authorYung, LYL
dc.date.accessioned2020-05-29T09:06:56Z
dc.date.available2020-05-29T09:06:56Z
dc.date.issued2018-01-01
dc.identifier.citationAng, YS, Woon, WWE, Yung, LYL (2018-01-01). The role of spacer sequence in modulating turn-on fluorescence of DNA-templated silver nanoclusters. Nucleic Acids Research 46 (14) : 6974-6982. ScholarBank@NUS Repository. https://doi.org/10.1093/nar/gky521
dc.identifier.issn03051048
dc.identifier.issn13624962
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/168694
dc.description.abstract© The Author(s) 2018. Published by Oxford University Press on behalf of Nucleic Acids Research. Guanine activation of fluorescence in DNA templated silver nanoclusters (AgNCs) is an interesting physical phenomenon which has yet to be fully understood to date. While the individual role of cytosine and guanine has been established, there is still a knowledge gap on how the AgNC-DNA system switches from dark to bright state. Here, we present evidence on the universal role of the DNA spacer sequence in physically separating two Ag+-binding cytosine sites to maintain the dark state while holding them together for structural re-organization by the guanine-rich strand to activate the bright state. The extent of turn-on signal could be modulated by adjusting the spacer length and composition. The ATATA spacer sequence was found to have negligible dark state fluorescence and a turn-on effect of 2440-fold, which was almost five times of the highest factor reported to date.
dc.publisherOxford University Press (OUP)
dc.sourceElements
dc.subjectBase Sequence
dc.subjectCytosine
dc.subjectDNA
dc.subjectFluorescence
dc.subjectNanostructures
dc.subjectNucleotides
dc.subjectSilver
dc.subjectTemplates, Genetic
dc.typeArticle
dc.date.updated2020-05-27T15:03:50Z
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1093/nar/gky521
dc.description.sourcetitleNucleic Acids Research
dc.description.volume46
dc.description.issue14
dc.description.page6974-6982
dc.published.statePublished
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