College of Chemistry and Environment, Fujian Province Key Laboratory of Morden Analytical Science and Separation Technology, Minnan Normal University, Zhangzhou, 363000, People's Republic of China.
Departement of Food and Biological Engineering, Zhangzhou Institute of Technology, Zhangzhou, 363000, People's Republic of China.
Mikrochim Acta. 2018 Nov 21;185(12):555. doi: 10.1007/s00604-018-3097-7.
An impedimetric method is described for ultrasensitive analysis of mercury(II). It is based on thymine-Hg(II)-thymine interaction which causes the disintegration of multiple-sandwich structured DNA chains. DNA strands were selected that are partially complementary to the T-rich Hg(II)-specific oligonucleotides (MSO). They were immobilized on a gold electrode via Au-S interaction. Next, the MSO and the bridging strands (BS) that can connect adjacent MSOs were alternately attached through layer-by-layer hybridization. Thus, a multiple-sandwich structured interface in created that carries numerous MSOs. This leads to a change-transfer resistance (R) values of the electrode-electrolyte interface at faradic electrochemical impedance spectroscopy measurements in the presence of the hexacyanoferrate(II)/(III) redox probe at 0.2 V (vs. Ag/AgCl). If Hg(II) is added to the solution, the MSOs selectively interact with Hg(II) to produce T-Hg(II)-T structures. Hence, the multiple-sandwich hybridization chains become disintegrated, and this causes a decrease in resistivity. The effect can be used to quantify Hg(II) over an analytical range that extends over four orders of magnitude (1 fM to 10 pM), and it has a 0.16 fM limit of detection under optimal conditions. Graphical abstract An electrochemical sensor for femtomolar level detection of Hg is realized on the basis of thymine-Hg-thymine interaction which causes disintegration of multiple sandwich DNA hybridization strands.
一种基于胸腺嘧啶 - Hg(II) - 胸腺嘧啶相互作用的电化学传感器,用于检测痕量 Hg(II)。该相互作用导致多重夹心 DNA 杂交链的解体。选择部分互补于富含胸腺嘧啶的 Hg(II)特异性寡核苷酸 (MSO) 的 DNA 链。它们通过 Au-S 相互作用固定在金电极上。接下来,通过层层杂交将 MSO 和可以连接相邻 MSO 的桥接链 (BS) 交替连接。因此,在存在六氰合铁(II)/(III)氧化还原探针的情况下,在法拉第电化学阻抗谱测量中,在 0.2 V(相对于 Ag/AgCl)下,创建了带有多个 MSO 的多重夹心结构界面。这导致电极-电解质界面的转移电阻 (R) 值发生变化。如果将 Hg(II)加入溶液中,MSO 会选择性地与 Hg(II)相互作用生成 T-Hg(II)-T 结构。因此,多重夹心杂交链解体,电阻率降低。该效应可用于定量检测分析范围内四个数量级(1 fM 至 10 pM)的 Hg(II),在最佳条件下检测限为 0.16 fM。
基于胸腺嘧啶 - Hg(II) - 胸腺嘧啶相互作用导致多重夹心 DNA 杂交链解体的原理,实现了用于检测痕量 Hg 的电化学传感器。