Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/81780
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dc.contributor.authorSutarlie, Lauraen
dc.contributor.authorAung, Khin Moh Mohen
dc.contributor.authorLim, Michelle Gek Liangen
dc.contributor.authorLukman, Stevenen
dc.contributor.authorCheung, Edwinen
dc.contributor.authorSu, Xiaodien
dc.date.accessioned2016-07-20T04:44:09Zen
dc.date.accessioned2019-12-06T14:40:27Z-
dc.date.available2016-07-20T04:44:09Zen
dc.date.available2019-12-06T14:40:27Z-
dc.date.issued2014en
dc.identifier.citationSutarlie, L., Aung, K. M. M., Lim, M. G. L., Lukman, S., Cheung, E., & Su, X. (2014). Studying Protein–DNA Complexes Using Gold Nanoparticles by Exploiting Particle Aggregation, Refractive Index Change, and Fluorescence Quenching and Enhancement Principles. Plasmonics, 9(4), 753-763.en
dc.identifier.issn1557-1955en
dc.identifier.urihttps://hdl.handle.net/10356/81780-
dc.description.abstractGold nanoparticles (AuNPs) have a unique optical phenomena termed localized surface plasmon resonance that is determined by particle shape, size, interparticle distance (or aggregation status), and local refractive index. AuNPs can also modulate fluorescence emission of proximal fluorophores under the Förster resonance energy transfer and/or nanoparticle surface energy transfer mechanisms. In this study, we use AuNPs (13 and 100 nm in diameter) as sensing elements to study sequence-dependent protein–DNA interactions by exploring all possible principles, namely (1) particle aggregation based colorimetric sensing, (2) refractive index sensing, and (3) fluorescence quenching/enhancement based fluorimetric sensing, exemplified by transcription factors, i.e., FoxA1 and AP2γ, and their respective DNAs. We conclude that the first principle, i.e., particle aggregation-based colorimetric assay that measures preformed complex by exploring complex protection of AuNPs from salt-induced aggregation, is simple to use. However, its performance is protein specific. For second and third principles that measure on-particle complex formation, we prove that the fluorescence quenching/enhancement assays supported by AuNPs are more sensitive than assays exploiting analyte-binding induced refractive index principle. This study provides a comprehensive assessment of the versatility of AuNPs as sensing probes for studying bioaffinity interactions especially protein–DNA complexes. The discovery of the DNA binding properties of FoxA1 and AP-2γ is important in revealing their roles in gene regulation.en
dc.description.sponsorshipASTAR (Agency for Sci., Tech. and Research, S’pore)en
dc.language.isoenen
dc.relation.ispartofseriesPlasmonicsen
dc.rights© 2014 Springer Science+Business Media New York.en
dc.subjectProtein–DNA complexesen
dc.subjectGold nanoparticlesen
dc.titleStudying Protein–DNA Complexes Using Gold Nanoparticles by Exploiting Particle Aggregation, Refractive Index Change, and Fluorescence Quenching and Enhancement Principlesen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Biological Sciencesen
dc.identifier.doi10.1007/s11468-013-9655-2en
item.grantfulltextnone-
item.fulltextNo Fulltext-
Appears in Collections:SBS Journal Articles

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