Suppr超能文献

通过电化学生还原氧化石墨烯电极上DNA适配体的附着与脱离实现超痕量铅离子的电化学检测

Electrochemical Detection of Ultratrace Lead Ion through Attaching and Detaching DNA Aptamer from Electrochemically Reduced Graphene Oxide Electrode.

作者信息

Yu Su Hwan, Lee Chang-Seuk, Kim Tae Hyun

机构信息

Department of Chemistry, Soonchunhyang University, Asan 31538, Korea.

出版信息

Nanomaterials (Basel). 2019 May 30;9(6):817. doi: 10.3390/nano9060817.

Abstract

This paper describes a simple strategy for the ultratrace level detection of Pb ion based on G-quadruplex DNA and an electrochemically reduced graphene oxide (ERGO) electrode. First, ERGO was formed on a glassy carbon electrode (GCE) by the reduction of graphene oxide (GO) using cyclic voltammetry. Subsequently, a methylene blue (MB)-tagged, guanine-rich DNA aptamer (Apt) was attached to the surface of ERGO via π-π interaction, leading to the Apt-modified ERGO electrode. The presence of Pb could generate the folding of Apt to a G-quadruplex structure. The formation of G-quadruplex resulted in detaching the Apt from the ERGO/GCE, leading to a change in redox current of the MB tag. Electrochemical measurements showed the proposed sensor had an exceptional sensitivity for Pb with a linear range from 10 to 10 M and a detection limit of 0.51 fM. The sensor also exhibited high selectivity for Pb, as well as many other advantages, such as stability, reproducibility, regeneration, as well as simple fabrication and operation processes.

摘要

本文描述了一种基于G-四链体DNA和电化学还原氧化石墨烯(ERGO)电极的铅离子超痕量检测简单策略。首先,通过循环伏安法还原氧化石墨烯(GO)在玻碳电极(GCE)上形成ERGO。随后,通过π-π相互作用将亚甲基蓝(MB)标记的富含鸟嘌呤的DNA适配体(Apt)附着到ERGO表面,从而得到Apt修饰的ERGO电极。铅的存在会使Apt折叠成G-四链体结构。G-四链体的形成导致Apt从ERGO/GCE上脱离,从而导致MB标签的氧化还原电流发生变化。电化学测量表明,所提出的传感器对铅具有出色的灵敏度,线性范围为10至10 M,检测限为0.51 fM。该传感器对铅还表现出高选择性,以及许多其他优点,如稳定性、可重复性、可再生性,以及简单的制备和操作过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/405b/6630585/d4c416300a4a/nanomaterials-09-00817-sch001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验