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

被引:187
|
作者
Li, Ming [1 ]
Zhou, Xuejiao [2 ]
Guo, Shouwu [2 ]
Wu, Nianqiang [1 ]
机构
[1] W Virginia Univ, Dept Mech & Aerosp Engn, Morgantown, WV 26506 USA
[2] Shanghai Jiao Tong Univ, Natl Key Lab Micro Nano Fabricat Technol, Res Inst Micro Nano Sci & Technol, Key Lab Thin Film & Microfabricat,Minist Educ, Shanghai 200240, Peoples R China
来源
BIOSENSORS & BIOELECTRONICS | 2013年 / 43卷
关键词
Sensor; Fluorescence; Energy transfer; Graphene oxide; Quantum dot; Lead; GOLD NANOPARTICLES; SENSING BIOMOLECULES; HIGH SELECTIVITY; DNA; PLATFORM; NANOCRYSTALS; DNAZYME; SENSOR; IONS; FRET;
D O I
10.1016/j.bios.2012.11.039
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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 Pb2+ detection. When Pb2+ ions are present in the assay, the interaction of Pb2+ with the aptamer induces a conformational change in the aptamer, leading to the formation of a G-quadruplex/Pb2+ complex. As a result, the QDs that are linked to the G-quadruplex/Pb2+ complex are detached from the GO sheet, which "turns on" the fluorescence of the QDs. This sensor exhibits a limit of detection of 90 pM and excellent selectivity toward Pb2+ 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 Forster resonance energy transfer (FRET) process. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 74
页数:6
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