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Dopamine and Melamine Binding to Gold Nanoparticles Dominates Their Aptamer-Based Label-Free Colorimetric Sensing

机译:多巴胺和三聚氰胺与金纳米颗粒的结合占据了其基于适体的无标记比色感测

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摘要

Target directed aptamer adsorption by gold nanoparticles (AuNPs) has been widely used to develop label-free colorimetric biosensors. However, the potential interactions between target molecules and AuNPs have not been considered, which may lead to misinterpretation of analytical results. In this work, the detection of dopamine, melamine, and k(+) was studied as model systems to address this problem. First, dopamine and two control molecules all induced the aggregation of citrate-capped AuNPs with apparent K-d's of 5.8 mu M dopamine, 51.6 mu M norepinephrine, and 142 mu M tyramine. Isothermal titration calorimetry measured the aptamer K-d to be 1.9 mu M dopamine and 16.8 mu M norepinephrine, whereas tyramine cannot bind. Surface enhanced Raman spectroscopy confirmed direct adsorption of dopamine, and the adsorbed dopamine inhibited the adsorption of DNA. Using a typical salt-induced colorimetric detection protocol, a similar color response was observed regardless of the sequence of DNA, indicating the observed color change reflected the adsorption of dopamine by the AuNPs instead of the binding of dopamine by the aptamer. For this label-free sensor to work, the interaction between the target molecule and AuNPs should be very weak, while dopamine represents an example of strong interactions. For the other two systems, the melamine detection did not reflect aptamer binding either but the K+ detection did, suggesting melamine also strongly interacted with AuNPs, whereas K+ had very weak interactions with AuNPs. Since each target molecule is different, such target/AuNP interactions need to be studied case-by-case to ensure the sensing mechanism.
机译:Gold纳米颗粒(AUNP)的目标定向适体吸附已被广泛用于开发无标记的比色生物传感器。然而,尚未考虑靶分子和AUNP之间的潜在相互作用,这可能导致分析结果的误解。在这项工作中,研究了多巴胺,三聚氰胺和K(+)的检测为模型系统,以解决这个问题。首先,多巴胺和两种对照分子均诱导柠檬酸盖剖腹产的聚集,具有5.8μm多巴胺,51.6μm去甲肾上腺素和142μm酪胺的表观K-D。等温滴定热量测定测量适体K-D为1.9 mu m多巴胺和16.8μmnorepinephrine,而酪胺不能结合。表面增强拉曼光谱证实直接吸附多巴胺,吸附的多巴胺抑制DNA的吸附。使用典型的盐诱导的比色检测方案,无论DNA的序列如何,都观察到类似的颜色响应,表明观察到的颜色变化反映了肛门分子的多巴胺的吸附而不是由适体通过多巴胺的结合。对于这种无标签传感器工作,目标分子和AUNP之间的相互作用应非常弱,而多巴胺代表了强相互作用的一个例子。对于另外两个系统,三聚氰胺检测不反映适体结合,但K +检测表明,三聚氰胺也与AUNPS强烈相互作用,而K +与AUNPS相互作用。由于每个靶分子不同,因此需要研究这种目标/ AUNP相互作用,以逐壳来确保传感机制。

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  • 来源
    《Analytical chemistry》 |2020年第13期|共9页
  • 作者单位

    Univ Waterloo Dept Chem Waterloo ON N2L 3G1 Canada;

    Univ Waterloo Dept Chem Waterloo ON N2L 3G1 Canada;

    Univ Waterloo Dept Chem Waterloo ON N2L 3G1 Canada;

    Univ Waterloo Dept Chem Waterloo ON N2L 3G1 Canada;

    Univ Waterloo Dept Chem Waterloo ON N2L 3G1 Canada;

    Univ Waterloo Dept Chem Waterloo ON N2L 3G1 Canada;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
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