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Pb2+ 诱导 DNA 构象从发夹到 G-四链体的转变:Pb2+ 的电化学检测。

Pb2+ induced DNA conformational switch from hairpin to G-quadruplex: electrochemical detection of Pb2+.

机构信息

Department of Chemistry, Beijing Normal University, Beijing, 100875.

出版信息

Analyst. 2011 Jun 7;136(11):2367-72. doi: 10.1039/c1an15080d. Epub 2011 Apr 13.

Abstract

Conformational switch from hairpin DNA to G-quadruplex induced by Pb(2+) is studied by electrochemical impedance spectroscopy (EIS) in the presence of Fe(CN)(6) as the redox probe. In the presence of Pb(2+), the G-rich hairpin DNA opens the stem-loop and forms G-quadruplex structure, which gives rise to a sharp increase in the charge-transfer resistance (R(CT)) of the film reflected by the EIS. This structural change is also confirmed by circular dichroism (CD) measurements and UV-Vis spectroscopic analysis and calculated by density functional theory (DFT). On the basis of this, we develop a label-free electrochemical DNA biosensor for Pb(2+) detection. With increasing concentrations of Pb(2+), the differences in the charge-transfer resistance R(CT) before and after the Pb(2+) incubation is linearly dependent on the logarithm of Pb(2+) concentration within a range from 50 μM to 0.5 nM. The biosensor also exhibits good selectivity for Pb(2+) over other metal ions. This is a simple and label-free electrochemical method for Pb(2+) detection making use of the G-quadruplex.

摘要

通过电化学阻抗谱(EIS)在 Fe(CN)(6)作为氧化还原探针的存在下,研究了发夹 DNA 与 G-四链体之间由 Pb(2+)诱导的构象开关。在 Pb(2+)存在下,富含 G 的发夹 DNA 打开茎环并形成 G-四链体结构,这导致 EIS 反射的薄膜的电荷转移电阻 (R(CT)) 急剧增加。这种结构变化也通过圆二色性(CD)测量和紫外可见光谱分析得到证实,并通过密度泛函理论(DFT)进行了计算。在此基础上,我们开发了一种用于检测 Pb(2+)的无标记电化学 DNA 生物传感器。随着 Pb(2+)浓度的增加,Pb(2+)孵育前后电荷转移电阻 R(CT)的差异与 Pb(2+)浓度的对数呈线性关系,范围从 50 μM 到 0.5 nM。该生物传感器对 Pb(2+)具有良好的选择性,优于其他金属离子。这是一种简单且无标记的电化学方法,可利用 G-四链体检测 Pb(2+)。

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