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还原氧化石墨烯负载的铂纳米颗粒作为过氧化物酶模拟物用于比色法检测特定DNA序列。

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

作者信息

Chau Li Yin, He Qijin, Qin Ailin, Yip Shea Ping, Lee Thomas M H

机构信息

Interdisciplinary Division of Biomedical Engineering, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China.

出版信息

J Mater Chem B. 2016 Jun 21;4(23):4076-4083. doi: 10.1039/c6tb00741d. Epub 2016 May 24.

Abstract

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.

摘要

在本研究中,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,开发了一种用于特定DNA序列的简单且灵敏的比色检测平台。这种纳米复合材料兼具铂纳米颗粒(优异的类过氧化物酶活性)和还原氧化石墨烯(与单链而非双链DNA的π-堆积相互作用)的综合优势。在合成步骤中,催化活性强烈依赖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,该纳米复合材料在较宽的温度范围(4 - 90°C)和pH范围(1 - 13)内具有出色的稳定性。对于DNA检测,纳米复合材料对单链探针(在无靶标的情况下)的亲和力高于探针 - 靶标双链体。与探针结合的纳米复合材料能稳定抵抗盐诱导的聚集,因此向上清液中加入3,3',5,5'-四甲基联苯胺和过氧化氢后,会产生强烈的蓝色。该检测平台的线性范围和检测限分别为0.5 - 10 nM和0.4 nM。此外,该平台具有高特异性,肉眼可区分3个碱基错配的序列,通过吸光度测量可区分1个碱基错配的序列。此外,通过聚合酶链反应产物分析证明了该平台在实际样品检测中的适用性。综上所述,这个新平台非常适合即时检测和现场核酸检测。

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