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      Detection of lead (II) with a "turn-on" fluorescent biosensor based on energy transfer from CdSe/ZnS quantum dots to graphene oxide.

      Biosensors & Bioelectronics
      Biosensing Techniques, instrumentation, Cadmium Compounds, chemistry, Equipment Design, Equipment Failure Analysis, Fluorescence Resonance Energy Transfer, Graphite, Lead, analysis, Oxides, Quantum Dots, Selenium Compounds, Sulfides, Zinc Compounds

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          Abstract

          Graphene oxide (GO) sheets are mixed with the aptamer-functionalized CdSe/ZnS quantum dots (QDs). Consequently, the aptamer-conjugated QDs bind to the GO sheets to form a GO/aptamer-QD ensemble, which enables the energy transfer from the QDs to the GO sheets, quenching the fluorescence of QDs. The GO/aptamer-QD ensemble assay acts as a "turn-on" fluorescent sensor for Pb(2+) detection. When Pb(2+) ions are present in the assay, the interaction of Pb(2+) with the aptamer induces a conformational change in the aptamer, leading to the formation of a G-quadruplex/Pb(2+) complex. As a result, the QDs that are linked to the G-quadruplex/Pb(2+) complex are detached from the GO sheet, which "turns on" the fluorescence of the QDs. This sensor exhibits a limit of detection of 90pM and excellent selectivity toward Pb(2+) over a wide range of metal ions. The experiments have provided direct evidence that the fluorescence of QDs is quenched by GO via the nano-metal surface energy transfer (NSET) mechanism rather than the conventional Förster resonance energy transfer (FRET) process. Copyright © 2012 Elsevier B.V. All rights reserved.

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