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Efficient Fluorescence Resonance Energy Transfer between Quantum Dots and Gold Nanoparticles Based on Porous Silicon Photonic Crystal for DNA Detection

机译:基于多孔硅光子晶体的量子点与金纳米粒子之间的高效荧光共振能量转移,用于DNA检测

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A novel assembled biosensor was prepared for detecting 16S rRNA, a small-size persistent specific for Actinobacteria. The mechanism of the porous silicon (PS) photonic crystal biosensor is based on the fluorescence resonance energy transfer (FRET) between quantum dots (QDs) and gold nanoparticles (AuNPs) through DNA hybridization, where QDs act as an emission donor and AuNPs serve as a fluorescence quencher. Results showed that the photoluminescence (PL) intensity of PS photonic crystal was drastically increased when the QDs-conjugated probe DNA was adhered to the PS layer by surface modification using a standard cross-link chemistry method. The PL intensity of QDs was decreased when the addition of AuNPs-conjugated complementary 16S rRNA was dropped onto QDs-conjugated PS. Based on the analysis of different target DNA concentration, it was found that the decrease of the PL intensity showed a good linear relationship with complementary DNA concentration in a range from 0.25 to 10 μM, and the detection limit was 328.7 nM. Such an optical FRET biosensor functions on PS-based photonic crystal for DNA detection that differs from the traditional FRET, which is used only in liquid. This method will benefit the development of a new optical FRET label-free biosensor on Si substrate and has great potential in biochips based on integrated optical devices.
机译:制备了一种新颖的组装式生物传感器,用于检测16S rRNA,这是一种针对放线菌的小尺寸持久性特异性。多孔硅(PS)光子晶体生物传感器的机理基于通过DNA杂交的量子点(QD)和金纳米颗粒(AuNPs)之间的荧光共振能量转移(FRET),其中QD充当发射供体,AuNP充当荧光猝灭剂。结果显示,当使用标准交联化学方法通过表面修饰将QDs偶联的探针DNA粘附到PS层时,PS光子晶体的光致发光(PL)强度急剧增加。当将与AuNPs共轭的互补16S rRNA的滴加到与QDs共轭的PS上时,QDs的PL强度降低。通过对不同目标DNA浓度的分析,发现PL强度的降低在0.25至10μM的范围内与互补DNA浓度呈良好的线性关系,检出限为328.7 nM。这种光学FRET生物传感器可在基于PS的光子晶体上进行DNA检测,这不同于仅在液体中使用的传统FRET。该方法将有利于在Si基板上开发新型的光学FRET无标签生物传感器,并且在基于集成光学器件的生物芯片中具有巨大潜力。

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