State Key Joint Laboratory of ESPC, School of Environment, Tsinghua University, Beijing 100084, China; National Key Laboratory of Science & Technology on Micro/Nano Fabrication, Institute of Microelectronics, Peking University, Beijing 100871, China.
State Key Joint Laboratory of ESPC, School of Environment, Tsinghua University, Beijing 100084, China.
Environ Int. 2021 Jan;146:106181. doi: 10.1016/j.envint.2020.106181. Epub 2020 Oct 21.
Herein, we reported a homemade waveguide-based evanescent wave aptasensor for the facile online monitoring of mercury pollution. The aptasensor exploited the high selectivity of hairpin structure-based thymidine-Hg-thymidine coordination chemistry (T-T mismatch) for Hg recognition and the stably regenerable capability of DNA-functionalized waveguide surfaces. The presence of Hg caused the T-T mismatch of Cy5.5-labeled T-rich single-stranded DNA sequences. The formed hairpin structures blocked the further hybridization of T-rich single-stranded DNA sequences with the complementary DNA strands that are modified on the waveguide surface; this phenomenon was accompanied by the decrease in the fluorescent signals excited by the evanescent wave. The limit of detection in real water samples was determined to be 0.2 μg/L, which was comparable with that of 0.4 μg/L in an ultrapure water under controlled conditions. And the linear range was observed from 1.4 µg/L to 240.7 µg/L. The negligible environmental matrix effect on the performance ensured the reliability of the proposed aptasensor. Moreover, the cross reactivity of this method toward other investigated metal ions was negligible. Through the delicate surface modification with DNA molecules covalently, the chip was reused at least 31 times with a relative standard deviation (RSD) of less than 19%. A Hg pollution accident was successfully detected within 30 min, shedding new light in pollution monitoring, environment restoration, and emergency treatment.
在此,我们报道了一种基于波导的消逝波适体传感器,用于简便在线监测汞污染。该适体传感器利用基于发夹结构的胸腺嘧啶-Hg-胸腺嘧啶配位化学(T-T 错配)对 Hg 的高选择性和 DNA 功能化波导表面的稳定可再生能力。Hg 的存在导致 Cy5.5 标记的富含 T 的单链 DNA 序列发生 T-T 错配。形成的发夹结构阻止了富含 T 的单链 DNA 序列与修饰在波导表面上的互补 DNA 链的进一步杂交;这一现象伴随着由消逝波激发的荧光信号的减少。在实际水样中的检测限确定为 0.2μg/L,与在受控条件下的超纯水中的 0.4μg/L 相当。线性范围观察到从 1.4μg/L 到 240.7μg/L。对性能的微小环境基质效应确保了所提出的适体传感器的可靠性。此外,该方法对其他研究的金属离子的交叉反应性可以忽略不计。通过 DNA 分子的共价精细表面修饰,该芯片可至少重复使用 31 次,相对标准偏差(RSD)小于 19%。在 30 分钟内成功检测到汞污染事故,为污染监测、环境修复和紧急处理提供了新的思路。