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首页> 外文期刊>RSC Advances >Ultrasensitive DNA detection based on target-triggered rolling circle amplification and fluorescent poly(thymine)-templated copper nanoparticles
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Ultrasensitive DNA detection based on target-triggered rolling circle amplification and fluorescent poly(thymine)-templated copper nanoparticles

机译:基于目标触发滚环扩增和荧光聚胸腺嘧啶模板铜纳米颗粒的超灵敏DNA检测

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We describe a novel strategy for the ultrasensitive detection of target DNA based on rolling circle amplification (RCA) coupled with fluorescent poly(thymine)-templated copper nanoparticles (poly T-CuNPs). In the presence of target DNA, a padlock DNA probe that consists of two regions: a target DNA-specific region and a poly(adenine) region, is circularized by the ligation reaction, and the subsequent RCA reaction is promoted to generate long, concatemeric, single-stranded DNA (ssDNA) with a lot of repetitive poly T sequences. As a result, a large number of poly T-CuNPs are formed, exhibiting a highly fluorescent signal. However, in the absence of target DNA or in the presence of non-specific target DNA, the padlock DNA probe is not circularized and the subsequent RCA is not executed, leading to no production of fluorescent poly T-CuNPs. With this simple strategy, we successfully analyzed the target DNA with the ultralow detection limit of 7.79 aM, a value that is 3 or 7 orders of magnitude lower than those of previous RCA-based fluorescent DNA detection strategies. In addition, the developed system was demonstrated to selectively discriminate non-specific target DNAs with one-base mismatch, suggesting potential application in the accurate diagnosis of single nucleotide polymorphisms or mutations.
机译:我们描述了一种新的策略,用于基于滚动环扩增(RCA)与荧光聚(胸腺嘧啶)模板铜纳米颗粒(poly T-CuNPs)的目标DNA的超灵敏检测。在存在目标DNA的情况下,由两个区域组成的挂锁DNA探针:目标DNA特异性区域和聚腺嘌呤区域通过连接反应被环化,随后的RCA反应被促进生成长链状体,具有许多重复的poly T序列的单链DNA(ssDNA)。结果,形成大量的聚T-CuNP,表现出高荧光信号。但是,在不存在靶DNA或存在非特异性靶DNA的情况下,挂锁DNA探针未环化且未执行后续的RCA,导致没有荧光聚T-CuNP的产生。通过这种简单的策略,我们成功地分析了超低检测限为7.79 aM的目标DNA,该值比以前基于RCA的荧光DNA检测策略低3或7个数量级。此外,已开发的系统被证明可以选择性地区分具有一碱基不匹配的非特异性靶DNA,这暗示了其在单核苷酸多态性或突变的准确诊断中的潜在应用。

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