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Detection of Adenosine Triphosphate with an Aptamer Biosensor Based on Surface-Enhanced Raman Scattering

机译:基于表面增强拉曼散射的适体生物传感器检测三磷酸腺苷

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摘要

A simple, ultrasensitive, highly selective, and reagent-free aptamer-based biosensor has been developed for quantitative detection of adenosine triphosphate (ATP) using surface-enhanced Raman scattering (SERS). The sensor contains a SERS probe made of gold nanostar@Raman label@SiO_(2) core-shell nanoparticles in which the Raman label (malachite green isothiocyanate, MGITC) molecules are sandwiched between a gold nanostar core and a thin silica shell. Such a SERS probe brings enhanced signal and low background fluorescence, shows good water-solubility and stability, and exhibits no sign of photobleaching. The aptamer labeled with the SERS probe is designed to hybridize with the cDNA on a gold film to form a rigid duplex DNA. In the presence of ATP, the interaction between ATP and the aptamer results in the dissociation of the duplex DNA structure and thereby removal of the SERS probe from the gold film, reducing the Raman signal. The response of the SERS biosensor varies linearly with the logarithmic ATP concentration up to 2.0 nM with a limit of detection of 12.4 pM. Our work has provided an effective method for detection of small molecules with SERS.
机译:已开发出一种简单,超灵敏,高度选择性且不含试剂的适体生物传感器,用于使用表面增强拉曼散射(SERS)定量检测三磷酸腺苷(ATP)。该传感器包含一个由金纳米星@拉曼标记@SiO_(2)核-壳纳米粒子制成的SERS探针,其中拉曼标记(孔雀石绿异硫氰酸盐,MGITC)分子夹在金纳米星核和薄二氧化硅壳之间。这种SERS探针可增强信号强度并降低背景荧光,显示出良好的水溶性和稳定性,并且没有光漂白的迹象。用SERS探针标记的适体设计为与金膜上的cDNA杂交形成刚性双链DNA。在ATP存在下,ATP和适体之间的相互作用导致双链DNA结构的解离,从而从金膜上去除了SERS探针,从而降低了拉曼信号。 SERS生物传感器的响应随对数ATP浓度高达2.0 nM线性变化,检出限为12.4 pM。我们的工作为使用SERS检测小分子提供了有效的方法。

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