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dc.contributor.authorLin, Wei Ting David
dc.contributor.authorHuang, Po-Jung Jimmy
dc.contributor.authorPautler, Rachel
dc.contributor.authorLiu, Juewen
dc.date.accessioned2017-02-27 20:36:50 (GMT)
dc.date.available2017-02-27 20:36:50 (GMT)
dc.date.issued2014-07-18
dc.identifier.urihttp://dx.doi.org/10.1039/C4CC05551A
dc.identifier.urihttp://hdl.handle.net/10012/11369
dc.description.abstractUsing sensitized Tb3+ luminescence spectroscopy as a tool, binding of 14 lanthanides to a lanthanide-dependent DNAzyme is studied, where the binding affinity is symmetric across the series and the tightest binding occurs with Nd3+ and Ho3+. This trend does not correlate with DNAzyme activity, suggesting that metal binding may not be the rate-limiting step of the DNAzyme catalysis.en
dc.description.sponsorshipUniversity of Waterloo || Canadian Foundation for Innovation || Natural Sciences and Engineering Research Council || Ontario Ministry of Research and Innovation ||en
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.subjectDNAen
dc.subjectDNAzymesen
dc.subjectmetal bindingen
dc.subjectCleavageen
dc.titleThe group trend of lanthanides binding to DNA and DNAzymes with a complex but symmetric patternen
dc.typeArticleen
dcterms.bibliographicCitationLin, W. T. D., Huang, P.-J. J., Pautler, R., & Liu, J. (2014). The group trend of lanthanides binding to DNA and DNAzymes with a complex but symmetric pattern. Chem. Commun., 50(80), 11859–11862. https://doi.org/10.1039/C4CC05551Aen
uws.contributor.affiliation1Faculty of Scienceen
uws.contributor.affiliation2Chemistryen
uws.contributor.affiliation2Waterloo Institute for Nanotechnology (WIN)en
uws.typeOfResourceTexten
uws.peerReviewStatusRevieweden
uws.scholarLevelFacultyen


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