Mei Zhong, Tang Liang
Department of Biomedical Engineering, University of Texas at San Antonio , San Antonio, Texas 78249, United States.
Anal Chem. 2017 Jan 3;89(1):633-639. doi: 10.1021/acs.analchem.6b02797. Epub 2016 Dec 19.
An innovative gold nanorod (GNR) array biochip was developed to systematically investigate the localized surface plasmon resonance (LSPR)-coupled fluorescence enhancement for signal amplification in molecular beacon detection. An ordered GNR assembly in vertical standing array on a glass surface was fabricated as plasmonic substrates, resulting in dramatically intensified LSPR between adjacent nanoparticles as compared to that from an ensemble of random nanorods. We have shown that the plasmonic response of the nanoarray can be tuned by the proper choice of GNR size to overlap the fluorophore excitation and emission wavelengths greater than 600 nm. Plasmon-induced fluorescence enhancement was found to be distance-dependent with the competition between quenching and enhancement by the metal nanostructures. The augmented fluorescence enhancement by the GNR array can efficiently overcome the quenching effect of the gold nanoparticle even at close proximity. The enhancement correlates with the spectral overlap between the fluorophore excitation/emission and the plasmonic resonance of the GNR array, indicating a surface-plasmon-enhanced excitation and radiative mechanism for the amplification. From these results, the applicability of the ordered GNR array chip was extended to molecular fluorescence enhancement for practical use as a highly functional and ultrasensitive plasmonic DNA biochip in molecular beacon fashion.
开发了一种创新的金纳米棒(GNR)阵列生物芯片,用于系统研究局域表面等离子体共振(LSPR)耦合荧光增强,以在分子信标检测中进行信号放大。在玻璃表面制备了垂直排列的有序GNR组件作为等离子体基底,与随机纳米棒集合相比,相邻纳米颗粒之间的LSPR显著增强。我们已经表明,可以通过适当选择GNR尺寸来调节纳米阵列的等离子体响应,使其与大于600nm的荧光团激发和发射波长重叠。发现等离子体诱导的荧光增强与距离有关,金属纳米结构在猝灭和增强之间存在竞争。即使在非常接近的距离,GNR阵列增强的荧光也能有效克服金纳米颗粒的猝灭效应。这种增强与荧光团激发/发射和GNR阵列的等离子体共振之间的光谱重叠相关,表明存在表面等离子体增强的激发和辐射放大机制。基于这些结果,有序GNR阵列芯片的适用性扩展到分子荧光增强,可实际用作分子信标形式的高功能超灵敏等离子体DNA生物芯片。