School of Marine Science and Technology, Harbin Institute of Technology, Weihai, 264209, People's Republic of China.
Anal Bioanal Chem. 2021 Nov;413(28):7001-7007. doi: 10.1007/s00216-021-03657-1. Epub 2021 Sep 16.
A novelty aptasensor for ultrasensitive detection of Hg is developed, exploiting the combination of plasmonic properties of gold nanoparticles (AuNPs) and exonuclease III (Exo III)-assisted target recycling for signal amplification. In the presence of Hg, a DNA duplex can be formed due to the strong coordination of Hg and T bases of single-stranded DNA (ssDNA) probe. Exo III digests the DNA duplex from the 3' to 5' direction, resulting in the releasing of Hg. Then, the released Hg binds with another ssDNA probe through T-Hg-T coordination. After Exo III-assisted Hg cycles, numerous ssDNA probes are exhausted, which promotes poly(diallyldimethylammonium chloride) (PDDA)-induced AuNP aggregation, leading to an obvious color change and aggregation-induced plasmon red shift of AuNPs (from 520 to 610 nm). Therefore, this biosensor is ultrasensitive, which is applicable to the detection of trace level of Hg with a linear range from 5 pM to 0.6 nM and an ultralow detection limit of 0.2 pM. Furthermore, it enables visual detection of Hg as low as 50 pM by the naked eye. More importantly, the assay can be applied to the reliable determination of spiked Hg in sea water samples with good recovery.
开发了一种新颖的适体传感器,用于超灵敏检测 Hg,利用金纳米粒子(AuNPs)的等离子体特性和外切酶 III(Exo III)辅助的靶标循环用于信号放大的组合。在存在 Hg 的情况下,由于 Hg 和单链 DNA(ssDNA)探针中 T 碱基的强配位,可以形成 DNA 双链。Exo III 从 3'到 5'方向消化 DNA 双链,导致 Hg 的释放。然后,释放的 Hg 通过 T-Hg-T 配位与另一个 ssDNA 探针结合。在 Exo III 辅助的 Hg 循环之后,大量的 ssDNA 探针被耗尽,这促进了聚二烯丙基二甲基氯化铵(PDDA)诱导的 AuNP 聚集,导致 AuNP 的明显颜色变化和聚集诱导的等离子体红移(从 520 到 610nm)。因此,该生物传感器具有超灵敏性,可用于检测痕量 Hg,线性范围为 5 pM 至 0.6 nM,检测限低至 0.2 pM。此外,它可以通过肉眼实现低至 50 pM 的 Hg 的可视化检测。更重要的是,该测定法可用于可靠测定海水中加标 Hg,回收率良好。