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Platinum nanoparticles on reduced graphene oxide as peroxidase mimetics for the colorimetric detection of specific DNA sequence

机译:还原氧化石墨烯上的铂纳米颗粒作为过氧化物酶模拟物,用于比色检测特定DNA序列

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摘要

In this work, we developed a simple and sensitive colorimetric detection platform for specific DNA sequences by using peroxidase mimetics of platinum nanoparticles supported on reduced graphene oxide. This nanocomposite possessed the combined advantages of platinum nanoparticles (superior peroxidase-like activity) and reduced graphene oxide (π-stacking interaction with single-stranded but not double-stranded DNA). The catalytic activity was strongly dependent on the chloroplatinic acid-to-graphene oxide mass ratio during the synthesis step, with an optimum ratio of 7:1. Unlike natural peroxidase, the nanocomposite had excellent stability over wide ranges of temperature (4-90 °C) and pH (1-13). For DNA detection, the nanocomposite had higher affinity for the single-stranded probe (in the absence of target) than the probe-target duplex. The probe-bound nanocomposite was stabilized against salt-induced aggregation and thus upon the addition of 3,3′,5,5′-tetramethylbenzidine and hydrogen peroxide to the supernatant, an intense blue color was generated. The linear range and limit of detection of this assay platform were 0.5-10 nM and 0.4 nM, respectively. Moreover, this platform featured high specificity that 3-base-mismatched sequence could be distinguished with the naked eye and 1-base-mismatched sequence with absorbance measurement. Furthermore, the applicability for real sample detection was demonstrated by polymerase chain reaction product analysis. Taken together, this new platform is well suited for point-of-care and on-site nucleic acid testing.
机译:在这项工作中,我们通过使用负载在还原氧化石墨烯上的铂纳米颗粒的过氧化物酶模拟物,为特定的DNA序列开发了一个简单而灵敏的比色检测平台。这种纳米复合材料具有铂纳米颗粒(具有超强的过氧化物酶活性)和减少的氧化石墨烯(与单链而不是双链DNA的π堆积相互作用)的综合优势。在合成步骤中,催化活性强烈取决于氯铂酸与氧化石墨烯的质量比,最佳比例为7:1。与天然过氧化物酶不同,该纳米复合材料在很宽的温度范围(4-90°C)和pH值(1-13)下具有出色的稳定性。对于DNA检测,纳米复合材料对单链探针(在没有靶标的情况下)具有比探针-靶标双链体更高的亲和力。使探针结合的纳米复合材料稳定,以防止盐诱导的聚集,因此在向上清液中添加3,3',5,5'-四甲基联苯胺和过氧化氢后,会产生深蓝色。该测定平台的线性范围和检测极限分别为0.5-10 nM和0.4 nM。此外,该平台具有很高的特异性,可以用肉眼识别3个碱基不匹配的序列,并通过吸光度测量来区分1个碱基不匹配的序列。此外,通过聚合酶链反应产物分析证明了实际样品检测的适用性。总而言之,这个新平台非常适合现场护理和现场核酸测试。

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