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Fluorescence Resonance Energy Transfer between Quantum Dots and Graphene Oxide for Sensing Biomolecules

机译:量子点和氧化石墨烯之间的荧光共振能量转移,用于传感生物分子

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摘要

This work designed a novel platform for effective sensingnof biomolecules by fluorescence resonance energy transfern(FRET) from quantum dots (QDs) to graphene oxide (GO).nThe QDs were first modified with a molecular beaconn(MB) as a probe to recognize the target analyte. The strongninteraction between MB and GO led to the fluorescentnquenching of QDs. Upon the recognition of the target, thendistance between the QDs and GO increased, and theninteraction between target-bound MB and GO becamenweaker, which significantly hindered the FRET and, thus,nincreased the fluorescence of QDs. The change in fluorescentnintensity produced a novel method for detectionnof the target. The GO-quenching approach could be usednfor detection of DNA sequences, with advantages such asnless labor for synthesis of the MB-based fluorescentnprobe, high quenching efficiency and sensitivity, and goodnspecificity. By substituting the MB with aptamer, thisnstrategy could be conveniently extended for detection ofnother biomolecules, which had been demonstrated by theninteraction between aptamer and protein. To the best ofnour knowledge, this is the first application of the FRETnbetween QDs and GO and opens new opportunities fornsensitive detection of biorecognition events.
机译:这项工作设计了一个新的平台,通过从量子点(QD)到氧化石墨烯(GO)的荧光共振能量转移(FRET)有效地感测生物分子.n首先将QDs修饰为分子信标(MB)作为探针以识别目标分析物。 MB和GO之间的强相互作用导致QD的荧光猝灭。一旦识别出目标,则量子点和GO之间的距离增加,然后与目标结合的MB和GO之间的相互作用变得更弱,这严重阻碍了FRET,从而增加了量子点的荧光。荧光强度的变化产生了一种检测靶标的新方法。 GO猝灭法可用于DNA序列的检测,具有合成基于MB的荧光探针无需人工,淬灭效率高,灵敏度高,特异性好等优点。通过用适体替代MB,该策略可以方便地扩展到检测其他生物分子,这已经通过适体与蛋白质之间的相互作用得到了证明。据我们所知,这是QD和GO之间FRETn的首次应用,为生物识别事件的灵敏检测开辟了新的机会。

著录项

  • 来源
    《Analytical Chemistry》 |2010年第13期|p.5511-5517|共7页
  • 作者单位

    Key Laboratory of Analytical Chemistry for Life Science (Ministry of Education of China), Department of Chemistry,Nanjing University, Nanjing 210093, Jiangsu Institute of Cancer Prevention and Cure, Nanjing 210009, P.R. China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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