Biosensing based upon molecular confinement in metallic nanocavity arrays

Yongdong Liu, Steve Blair
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引用次数: 71

Abstract

Research world-wide on biosensing techniques is motivated by numerous applications in clinical diagnostics, genetic screenings, proteomics, and single-molecule detection, for example. However, the important problem of detecting in parallel a large number of molecular species from very small samples remains an elusive goal. This work represents a step in that direction through the development of a biosensor platform in which enhanced fluorescence transduction occurs through the optical excitation of molecules located within metallic nanocavities. This study also demonstrates that the phenomenon of enhanced transmission can be used as a technique for molecular transduction in optical biosensor applications with the important benefits of an apparent increase in fluorescence yield and isolation from fluorescence produced by unbound species. Finally, we demonstrate that real-time biosensing can be performed by monitoring the fluorescence signal produced due to the hybridization between probe oligonucleotide's immobilized within the nanocavities and complementary target oligonucleotides in solution introduced through a microfluidic channel.
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基于分子约束的金属纳米腔阵列生物传感
例如,生物传感技术在临床诊断、遗传筛查、蛋白质组学和单分子检测等领域的大量应用推动了世界范围内对生物传感技术的研究。然而,从非常小的样本中并行检测大量分子物种的重要问题仍然是一个难以实现的目标。通过开发生物传感器平台,这项工作代表了朝着这个方向迈出的一步,在该平台中,通过位于金属纳米腔内的分子的光学激发来增强荧光转导。该研究还表明,增强透射现象可以用作光学生物传感器应用中的分子转导技术,其重要好处是荧光产量明显增加,并且可以从非结合物种产生的荧光中分离出来。最后,我们证明了实时生物传感可以通过监测固定在纳米腔内的探针寡核苷酸和通过微流控通道引入溶液中的互补目标寡核苷酸之间杂交产生的荧光信号来实现。
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