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A silver-specific DNA-based bio-assay for Ag(I) detection via the aggregation of unmodified gold nanoparticles in aqueous solution coupled with resonance Rayleigh scattering

机译:通过基于水溶液的未修饰金纳米粒子的聚集以及共振瑞利散射,通过银特定的基于DNA的Ag(I)生物检测方法

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We report a label-free, silver-specific DNA-based bio-assay for the detection of silver ion (Ag~+) in aqueous solution. The bio-assay relies on the structural change of cytosine (C)-rich silver-specific DNA and the status transition of gold nanoparticles (AuNPs). In the absence of Ag~+, unfolded silver-specific DNA stabilizes the dispersed AuNPs at high salt concentrations, which induces low resonance Rayleigh scattering (RRS) intensity. However, in the presence of Ag~+, silver-specific DNA folds into a hairpin conformation through C-Ag~+-C mismatches, and cannot coat on the surface of AuNPs. Thus, the uncoated AuNPs aggregate at high salt concentrations and cause a significant increase in RRS intensity, which reflects the amount of Ag~+ in the system. Under the optimized conditions, the RRS intensity at 550 nm increased linearly with the concentration of Ag~+ ranging from 0.20 μM to 1.00 μM, and the limit of detection for Ag~+ was determined as 0.202 μM. The bio-assay also shows high selectivity against coexisting cations.
机译:我们报告了一种无标记,基于银的特定DNA的生物检测方法,用于检测水溶液中的银离子(Ag〜+)。生物测定依赖于富含胞嘧啶(C)的银特异性DNA的结构变化和金纳米颗粒(AuNPs)的状态转变。在没有Ag +的情况下,未折叠的银特异性DNA使分散的AuNPs在高盐浓度下稳定,从而引起低共振瑞利散射(RRS)强度。但是,在存在Ag〜+的情况下,银特异性DNA通过C-Ag〜+ -C错配折叠成发夹构型,并且不能覆盖在AuNPs的表面。因此,未包被的AuNPs在高盐浓度下聚集并导致RRS强度显着增加,这反映了系统中Ag +的量。在最佳条件下,550nm处的RRS强度随着Ag〜+的浓度从0.20μM到1.00μM线性增加,测定的Ag〜+的检出限为0.202μM。该生物测定法还显示出对共存阳离子的高选择性。

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