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Detection of nuclease activity using a simple fluorescence based biosensor

机译:使用基于荧光的简单生物传感器检测核酸酶活性

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摘要

Nucleases are associated with a variety of diseases as they catalyze the degradation of nucleic acids. Their presence as a contaminant could also be a major concern in several molecular biology-related analyses where DNAse and RNAse free environments are required. Here, we report a simple, fluorescence-based biosensor for nuclease detection. The sensor utilizes only one fluorescent molecule attached to a ssDNA molecule building upon a fluorescence-quenching phenomenon taking place between a fluorescent dye and a nucleotide base. The intensity of the fluorescent molecule is quenched by covalently attaching to ssDNA and upon digestion of the ssDNA the fluorescence signal increases dramatically. Consequently, the fluorescence signal can be used to determine the activity of nuclease enzymes for a variety of applications ranging from molecular biology to clinical diagnostics. Compared to available methods, our sensor does not use any additional substances such as cationic polymers, carbon nanotubes or nanoparticles, graphene oxide or silver nanoclusters or a quencher like DABCYL to quench a fluorophore. The simplicity of the detection method makes this an attractive sensor as a low cost, fast and convenient system that can be incorporated into multiple readers for widespread use in virtually all molecular biology-related analyses.
机译:核酸酶与多种疾病有关,因为它们催化核酸的降解。在需要DNAse和RNAse无环境的一些分子生物学相关分析中,它们作为污染物的存在也可能是一个主要问题。在这里,我们报告一个简单的基于荧光的核酸酶检测生物传感器。该传感器仅利用附着在ssDNA分子上的一个荧光分子,该荧光分子建立在荧光染料和核苷酸碱基之间发生的荧光猝灭现象的基础上。荧光分子的强度通过与ssDNA共价结合而猝灭,并且在消化ssDNA时,荧光信号急剧增加。因此,荧光信号可用于确定核酸酶的活性,适用于从分子生物学到临床诊断的各种应用。与可用方法相比,我们的传感器不使用任何其他物质(例如阳离子聚合物,碳纳米管或纳米颗粒,氧化石墨烯或银纳米簇)或淬灭剂(如DABCYL)来淬灭荧光团。检测方法的简便性使其成为一种低成本,快速且方便的系统,可以被并入多个读取器中,从而在几乎所有与分子生物学相关的分析中广泛使用,因此成为一种有吸引力的传感器。

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