Key Laboratory of Analysis and Detection for Food Safety (MOE & Fujian Province), Institute of Nanomedicine and Nanobiosensing, Department of Chemistry, Fuzhou University, Fuzhou 350108, PR China.
Key Laboratory of Analysis and Detection for Food Safety (MOE & Fujian Province), Institute of Nanomedicine and Nanobiosensing, Department of Chemistry, Fuzhou University, Fuzhou 350108, PR China.
Biosens Bioelectron. 2016 May 15;79:411-5. doi: 10.1016/j.bios.2015.12.081. Epub 2015 Dec 23.
A new label-free DNA sensing protocol was designed for fluorescent detection of mercury(II) (Hg(2+)), coupling hairpin DNA-scaffolded silver nanocluster (DNA-AgNC) with exonuclease III-assisted target recycling amplification. The assay was carried out through target-induced conformational change of hairpin DNA, while the signal derived from the formed silver nanoclusters on hairpin DNA probes. Initially, target Hg(2+) was specifically coordinated with thymine-thymine (T-T) mismatches to form an intact hairpin DNA. Then, the newly formed hairpin DNA was digested through exonuclease III from blunt 3' termini and restrained at 3' protruding terminus, thus resulting in the release of target Hg(2+) from hairpin DNA. The liberated target Hg(2+) initiated the next cycling, thereby causing the conformational change of numerous hairpin probes from the stem-loop DNA structure to single-stranded DNA. Under the optimal conditions, the fluorescent intensity of the as-produced DNA-AgNCs decreased with the increasing Hg(2+) concentration within a dynamic range from 0.1 nM to 10nM with a detection limit (LOD) of 24 pM. Moreover, the low-cost fluorescent sensing system exhibited high reproducibility and good specificity, thus representing an optional sensing platform for rapid screening of Hg(2+) in environmental water samples.
设计了一种新的无标记 DNA 传感方案,用于荧光检测汞(II) (Hg(2+)),将发夹 DNA 支架银纳米团簇 (DNA-AgNC) 与外切酶 III 辅助的目标循环放大相结合。该测定通过发夹 DNA 的目标诱导构象变化进行,而信号则源自发夹 DNA 探针上形成的银纳米团簇。最初,目标 Hg(2+) 特异性地与胸腺嘧啶-胸腺嘧啶 (T-T) 错配结合形成完整的发夹 DNA。然后,新形成的发夹 DNA 通过外切酶 III 从平头 3'末端消化,并限制在 3'突出末端,从而导致发夹 DNA 中目标 Hg(2+) 的释放。释放的目标 Hg(2+) 引发下一个循环,从而导致大量发夹探针从茎环 DNA 结构到单链 DNA 的构象变化。在最佳条件下,产生的 DNA-AgNC 的荧光强度随 Hg(2+)浓度的增加而降低,在 0.1 nM 至 10 nM 的动态范围内具有检测限 (LOD) 为 24 pM。此外,该低成本荧光传感系统表现出高重现性和良好的特异性,因此代表了一种可选的传感平台,可用于快速筛选环境水样中的 Hg(2+)。