Suppr超能文献

基于自主组装血红素/G-四链体 DNA 酶纳米线用于信号放大的汞(II)离子灵敏假酶电化学生物传感器。

Sensitive pseudobienzyme electrocatalytic DNA biosensor for mercury(II) ion by using the autonomously assembled hemin/G-quadruplex DNAzyme nanowires for signal amplification.

机构信息

Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China; College of resources and environments, Southwest University, Chongqing 400715, PR China.

Key Laboratory on Luminescence and Real-Time Analysis, Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.

出版信息

Anal Chim Acta. 2014 Feb 6;811:23-8. doi: 10.1016/j.aca.2013.11.051. Epub 2013 Dec 6.

Abstract

Herein, a novel sensitive pseudobienzyme electrocatalytic DNA biosensor was proposed for mercury ion (Hg(2+)) detection by using autonomously assembled hemin/G-quadruplex DNAzyme nanowires for signal amplification. Thiol functionalized capture DNA was firstly immobilized on a nano-Au modified glass carbon electrode (GCE). In presence of Hg(2+), the specific coordination between Hg(2+) and T could result in the assembly of primer DNA on the electrode, which successfully triggered the HCR to form the hemin/G-quadruplex DNAzyme nanowires with substantial redox probe thionine (Thi). In the electrolyte of PBS containing NADH, the hemin/G-quadruplex nanowires firstly acted as an NADH oxidase to assist the concomitant formation of H2O2 in the presence of dissolved O2. Then, with the redox probe Thi as electron mediator, the hemin/G-quadruplex nanowires acted as an HRP-mimicking DNAzyme that quickly bioelectrocatalyzed the reduction of produced H2O2, which finally led to a dramatically amplified electrochemical signal. This method has demonstrated a high sensitivity of Hg(2+) detection with the dynamic concentration range spanning from 1.0 ng L(-1) to 10 mg L(-1) Hg(2+) and a detection limit of 0.5 ng L(-1) (2.5 pM) at the 3Sblank level, and it also demonstrated excellent selectivity against other interferential metal ions.

摘要

在此,通过自主组装血红素/G-四链体 DNA 酶纳米线进行信号放大,提出了一种用于汞离子(Hg(2+))检测的新型敏感假酶电化学生物传感器。首先将巯基功能化的捕获 DNA 固定在纳米 Au 修饰的玻碳电极 (GCE) 上。存在 Hg(2+)时,Hg(2+)与 T 的特异性配位导致在电极上组装引物 DNA,成功触发 HCR 形成具有大量氧化还原探针硫堇 (Thi) 的血红素/G-四链体 DNA 酶纳米线。在含有 NADH 的 PBS 电解质中,血红素/G-四链体纳米线首先充当 NADH 氧化酶,在溶解氧存在的情况下协助同时形成 H2O2。然后,以氧化还原探针 Thi 作为电子介体,血红素/G-四链体纳米线充当 HRP 模拟 DNA 酶,快速生物电催化产生的 H2O2 的还原,最终导致电化学信号大大放大。该方法对 Hg(2+)的检测具有很高的灵敏度,动态浓度范围从 1.0 ng L(-1)到 10 mg L(-1) Hg(2+),在 3Sblank 水平下检测限为 0.5 ng L(-1) (2.5 pM),并且对其他干扰金属离子具有优异的选择性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验