首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >A simple 'clickable' biosensor for colorimetric detection of copper(II) ions based on unmodified gold nanoparticles
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A simple 'clickable' biosensor for colorimetric detection of copper(II) ions based on unmodified gold nanoparticles

机译:一种简单的“可点击”生物传感器,用于基于未修饰的金纳米粒子的比色检测铜(II)离子

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摘要

A novel colorimetric copper(II) biosensor has been developed based on the high specificity of alkyne-azide click reaction to the catalysis of copper ions and unmodified gold nanoparticles (AuNPs) as the signal reporter. The clickable DNA probe consists of two parts: an azide group-modified double-stranded DNA (dsDNA) hybrid with an elongated tail and a short alkyne-modified single-stranded DNA (ssDNA). Because of low melting temperature of the short ssDNA, these two parts are separated in the absence of Cu~(2+). Copper ion-induced azide-alkyne click ligation caused a structural change of probe from the separated form to entire dsDNA form. This structural change of probe can be monitored by the unmodified AuNPs via mediating their aggregation with a red-to-blue colorimetric read-out because of the differential ability of ssDNA and dsDNA to protect AuNPs against salt-induced aggregation. Under the optimum conditions, this biosensor can sensitively and specifically detect Cu~(2+) with a low detection limit of 250nM and a linear range of 0.5-10μM. The method is simple and economic without dual-labeling DNA and AuNPs modification. It is also highly selective for Cu~(2+) in the presence of high concentrations of other environmentally relevant metal ions because of the great specificity of the copper-caused alkyne-azide click reaction, which potentially meets the requirement of the detection in real samples.
机译:基于炔-叠氮化click点击反应对铜离子和未修饰的金纳米颗粒(AuNPs)催化的高特异性,已经开发出一种新型比色铜(II)生物传感器。可点击的DNA探针由两部分组成:叠氮基修饰的双链DNA(dsDNA)杂交体,带有长尾巴和短炔烃修饰的单链DNA(ssDNA)。由于短ssDNA的低解链温度,这两个部分在没有Cu〜(2+)的情况下被分离。铜离子诱导的叠氮化物-炔烃单击连接导致探针的结构从分离的形式变为整个dsDNA形式。由于ssDNA和dsDNA保护AuNPs免受盐诱导的聚集的能力不同,未修饰的AuNPs可以通过介导其聚集的红到蓝比色读数来监测探针的这种结构变化。在最佳条件下,该生物传感器能够以250nM的低检测限和0.5-10μM的线性范围灵敏,特异地检测Cu〜(2+)。该方法简单且经济,无需对DNA和AuNPs进行双标记修饰。在高浓度的其他与环境有关的金属离子存在下,它对Cu〜(2+)的选择性也很高,这是因为铜引起的炔叠氮点击反应的特异性很高,有可能满足实际检测的要求。样品。

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