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Polymerase chain reaction-free variable-number tandem repeat typing using gold nanoparticle-DNA monoconjugates

机译:使用金纳米粒子-DNA单缀合物的无聚合酶链反应的可变数目串联重复重复键入

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摘要

In this work, we report a novel polymerase chain reaction (PCR)-free variable-number tandem repeat (VNTR) typing method using a T-shaped gold nanoparticle-DNA monoconjugate, called the "watching-gene assay". The T-shaped DNA probe was synthesized by "click" chemistry and linked with the gold nanoparticle to form the gold nanoparticle-DNA monoconjugate (a VNTR probe). Through a simple annealing and ligation reaction of the VNTR probe on a synthetic DNA template mimicking the human D1S80 VNTR locus, the number of tandem repeat units could be deciphered by counting the self-assembled gold nanoparticles. The number of tandem repeat units could be identified with more than 50% yield if the repeat number was less than four. In the case of the real human genomic DNA, the 18 repeat unit number could be successfully revealed by observing the 18-gold-nanoparticle cluster, which exactly corresponded to the number of tandem repeats of the real sample. Our "watching-gene assay" is rapid, simple, and direct for data interpretation, thereby providing an advanced PCR-free genetic polymorphism analysis platform.
机译:在这项工作中,我们报告了一种新型的无聚合酶链反应(PCR)的可变数目串联重复重复(VNTR)分型方法,该方法使用T型金纳米颗粒-DNA单共轭物,称为“观察基因测定法”。通过“点击”化学合成T形DNA探针,并将其与金纳米颗粒连接以形成金纳米颗粒-DNA单缀合物(VNTR探针)。通过在模拟人D1S80 VNTR基因座的合成DNA模板上对VNTR探针进行简单的退火和连接反应,可以通过计算自组装金纳米粒子来破译串联重复单元的数量。如果重复数少于四个,则可以鉴定出串联重复单元的数量,收率超过50%。对于真正的人类基因组DNA,通过观察18个金纳米颗粒簇,可以成功揭示18个重复单元的数目,该簇恰好对应于真实样品的串联重复序列的数目。我们的“观察基因测定”快速,简单,直接地进行数据解释,从而提供了一种无需PCR的高级遗传多态性分析平台。

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