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Unusual sequence length-dependent gold nanoparticles aggregation of the ssDNA sticky end and its application for enzyme-free and signal amplified colorimetric DNA detection

机译:ssDNA粘性末端异常依赖序列长度的金纳米粒子聚集及其在无酶和信号放大比色DNA检测中的应用

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摘要

It is known that the adsorption of short single-stranded DNA (ssDNA) on unmodified gold nanoparticles (AuNPs) is much faster than that for long ssDNA, and thus leads to length-dependent AuNPs aggregation after addition of salt, the color of the solutions sequentially changed from red to blue in accordance with the increase of ssDNA length. However, we found herein that the ssDNA sticky end of hairpin DNA exhibited a completely different adsorption behavior compared to ssDNA, an inverse blue-to-red color variation was observed in the colloid solution with the increase of sticky end length when the length is within a certain range. This unusual sequence length-dependent AuNPs aggregation might be ascribed to the effect of the stem of hairpin DNA. On the basis of this unique phenomenon and catalytic hairpin assembly (CHA) based signal amplification, a novel AuNPs-based colorimetric DNA assay with picomolar sensitivity and specificity was developed. This unusual sequence length-dependent AuNPs aggregation of the ssDNA sticky end introduces a new direction for the AuNPs-based colorimetric assays.
机译:众所周知,短的单链DNA(ssDNA)在未修饰的金纳米颗粒(AuNPs)上的吸附比长的ssDNA吸附快得多,因此在添加盐,溶液颜色后会导致长度依赖性的AuNPs聚集。随着ssDNA长度的增加,顺序从红色变为蓝色。但是,我们在这里发现发夹DNA的ssDNA粘性末端与ssDNA相比表现出完全不同的吸附行为,在胶体溶液中观察到蓝到红颜色的反向变化,当长度在10s以内时,粘性末端长度增加一定范围内这种不寻常的依赖序列长度的AuNPs聚集可能归因于发夹DNA茎的作用。基于这种独特的现象和基于催化发夹装配(CHA)的信号放大,开发了一种基于AuNPs的新型比色DNA检测方法,具有皮摩尔灵敏度和特异性。 ssDNA粘性末端的这种不寻常的序列长度依赖性AuNPs聚集为基于AuNPs的比色测定法引入了新的方向。

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