Department of Chemistry, Capital Normal University, Beijing 100048, China.
Biosens Bioelectron. 2013 Oct 15;48:108-12. doi: 10.1016/j.bios.2013.04.007. Epub 2013 Apr 17.
Herein, a label-free and highly sensitive electrochemical impedance spectroscopy (EIS) aptasensor for the detection of potassium ion (K⁺) was developed based on a conformational change in which a K⁺-stabilized single stranded DNA (ssDNA) with G-rich sequence was used as the recognition element. In the measurement of K⁺ ions, the change in interfacial electron transfer resistance (R(ct)) of the sensor using a redox couple of [Fe(CN)₆]³⁻/⁴⁻ as the probe was monitored. In the presence of K⁺, the G-rich DNA folded into the G-quadruplex structure, and then K⁺ can bind to the G-quadruplex structure, leading to an increase in the R(ct). The Rct increased with K⁺ concentration, and the plot of R(ct) against the logarithm of K⁺ concentration is linear over the range from 0.1 nM to 1 mM with a detection limit of 0.1 nM. Other metal ions, such as Ca²⁺, Mg²⁺, Na⁺, Li⁺, Al³⁺, Zn²⁺, Cu²⁺, and Ni²⁺ caused no notable interference on the detection of K⁺. The scheme reported herein is applicable to the detection of other kinds of G-rich aptamer-binding chemicals and biomolecules.
本文基于构象变化,开发了一种无标记的、高灵敏度的电化学阻抗谱(EIS)适体传感器,用于检测钾离子(K⁺)。在该传感器中,使用富含 G 的序列作为识别元件的 K⁺稳定单链 DNA(ssDNA)。在测量 K⁺离子时,使用 [Fe(CN)₆]³⁻/⁴⁻作为探针监测传感器界面电子转移电阻(R(ct))的变化。在 K⁺存在下,富含 G 的 DNA 折叠成 G-四链体结构,然后 K⁺可以与 G-四链体结构结合,导致 R(ct)增加。Rct 随 K⁺浓度的增加而增加,R(ct)与 K⁺浓度的对数的关系呈线性,线性范围为 0.1 nM 至 1 mM,检测限为 0.1 nM。其他金属离子,如 Ca²⁺、Mg²⁺、Na⁺、Li⁺、Al³⁺、Zn²⁺、Cu²⁺和 Ni²⁺,对 K⁺的检测没有明显干扰。本文报道的方案适用于检测其他种类的富含 G 的适体结合化学物质和生物分子。