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量子点如何聚集增强荧光共振能量转移

How Quantum Dots Aggregation Enhances Förster Resonant Energy Transfer.

作者信息

Hottechamps Julie, Noblet Thomas, Brans Alain, Humbert Christophe, Dreesen Laurent

机构信息

GRASP-Biophotonics, CESAM, University of Liege, Institute of Physics, Allée du 6 août 17, 4000, Liège, Belgium.

Center for Protein Engineering (CIP), InBioS, University of Liege, Quartier Agora, Allée du six Août 13, B6a, 4000, Liège, Belgium.

出版信息

Chemphyschem. 2020 May 5;21(9):853-862. doi: 10.1002/cphc.202000067. Epub 2020 Apr 1.

Abstract

As luminescent quantum dots (QDs) are known to aggregate themselves through their chemical activation by carbodiimide chemistry and their functionalization with biotin molecules, we investigate both effects on the fluorescence properties of CdTe QDs and their impact on Förster Resonant Energy Transfer (FRET) occurring with fluorescent streptavidin molecules (FA). First, the QDs fluorescence spectrum undergoes significant changes during the activation step which are explained thanks to an original analytical model based on QDs intra-aggregate screening and inter-QDs FRET. We also highlight the strong influence of biotin in solution on FRET efficiency, and define the experimental conditions maximizing the FRET. Finally, a free-QD-based system and an aggregated-QD-based system are studied in order to compare their detection threshold. The results show a minimum concentration limit of 80 nM in FA for the former while it is equal to 5 nM for the latter, favouring monitored aggregation in the design of QDs-based biosensors.

摘要

由于已知发光量子点(QDs)可通过碳二亚胺化学对其进行化学活化以及用生物素分子进行功能化而发生聚集,我们研究了这两种情况对碲化镉量子点荧光特性的影响以及它们对与荧光链霉亲和素分子(FA)发生的荧光共振能量转移(FRET)的影响。首先,量子点荧光光谱在活化步骤中会发生显著变化,这借助基于量子点聚集体内筛选和量子点间FRET的原始分析模型得到了解释。我们还强调了溶液中生物素对FRET效率的强烈影响,并确定了使FRET最大化的实验条件。最后,研究了基于游离量子点的系统和基于聚集量子点的系统,以比较它们的检测阈值。结果表明,前者对FA的最低浓度限制为80 nM,而后者为5 nM,这有利于在基于量子点的生物传感器设计中监测聚集情况。

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