Please use this identifier to cite or link to this item: https://doi.org/10.1021/la102872v
DC FieldValue
dc.titleLRET-based biodetection of DNA release in live cells using surface-modified upconverting fluorescent nanoparticles
dc.contributor.authorGuo, H.
dc.contributor.authorIdris, N.M.
dc.contributor.authorZhang, Y.
dc.date.accessioned2014-06-17T09:44:59Z
dc.date.available2014-06-17T09:44:59Z
dc.date.issued2011-03-15
dc.identifier.citationGuo, H., Idris, N.M., Zhang, Y. (2011-03-15). LRET-based biodetection of DNA release in live cells using surface-modified upconverting fluorescent nanoparticles. Langmuir 27 (6) : 2854-2860. ScholarBank@NUS Repository. https://doi.org/10.1021/la102872v
dc.identifier.issn07437463
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/67146
dc.description.abstractIn this work, we demonstrate near-infrared-to-visible upconverting fluorescent nanoparticles as a promising platform for lanthanide-based or luminescence resonance energy transfer (LRET)-based biodetection of DNA release in live cells. Highly monodispersed, stable aqueous suspension of nanoparticles, surface-functionalized with amino groups for binding to DNA, were prepared and characterized. These amino-functionalized nanoparticles were able to electrostatically bind to DNA and protect it from DNaseI degradation as shown by gel electrophoresis. Attachment of DNA to the nanoparticles was also confirmed by LRET, which was observed to occur between the donor nanoparticle and acceptor POPO-3 dye intercalating the DNA. The intrinsic fluorescence property of upconverting fluorescent nanoparticles makes them useful for tracking their cellular localization without the use of any additional fluorescent tag. We were able to track the movement of these DNA-loaded nanoparticles into the cell cytoplasm where they successfully released their genetic cargo. Successful transfection of the loaded DNA material in vitro and in vivo was confirmed by expression of its encoded green fluorescent protein (GFP) in Hela cells and induction of specific antibody in mice, respectively. © 2011 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/la102872v
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOENGINEERING
dc.description.doi10.1021/la102872v
dc.description.sourcetitleLangmuir
dc.description.volume27
dc.description.issue6
dc.description.page2854-2860
dc.description.codenLANGD
dc.identifier.isiut000288039500103
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