Zou Rong, Wang Shuang, Chen Chunyan, Chen Xiaoming, Gong Hang, Cai Changqun
Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan, 411105, China.
Key Laboratory for Green Organic Synthesis and Application of Hunan Province, Key Laboratory of Environmentally Friendly Chemistry and Application of Ministry of Education, College of Chemistry, Xiangtan University, Xiangtan, 411105, China.
Talanta. 2021 Jan 15;222:121505. doi: 10.1016/j.talanta.2020.121505. Epub 2020 Aug 13.
A fluorescence strategy for highly sensitive and selective detection of H5N1 DNA was proposed based on MoS nanosheets and catalytic hairpin assembly. This platform not only avoided any labeling but also reduced the background signal. In the absence of target, CHA could not be triggered and the thiazole orange and MBs complexes were adsorbed on the surface of MoS to quench the fluorescence of TO, resulting in low background signal. However, upon addition of target DNA, the CHA was initiated and produced plenty of MBs duplex which could be far away from the surface of MoS and bind to TO to enhance its fluorescence. This approach exhibited excellent sensitivity and specificity for H5N1 DNA with a detection limit of 7.5 pM, and realized the assay of H5N1 DNA in human serum samples. Furthermore, this platform could be expanded to detect other virus DNA by changing the corresponding molecular beacons, holding the potential of clinical application.
基于二硫化钼纳米片和催化发夹组装,提出了一种用于高灵敏和选择性检测H5N1 DNA的荧光策略。该平台不仅避免了任何标记,还降低了背景信号。在没有靶标的情况下,催化发夹组装无法触发,噻唑橙和分子信标复合物吸附在二硫化钼表面,淬灭噻唑橙的荧光,导致背景信号较低。然而,加入靶标DNA后,催化发夹组装被启动,产生大量远离二硫化钼表面的分子信标双链体,并与噻唑橙结合以增强其荧光。该方法对H5N1 DNA表现出优异的灵敏度和特异性,检测限为7.5 pM,并实现了人血清样本中H5N1 DNA的检测。此外,通过改变相应的分子信标,该平台可扩展用于检测其他病毒DNA,具有临床应用潜力。