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基于配体响应的 G-四链体形成的 DNA 无标记生物传感器

A label-free biosensor for DNA detection based on ligand-responsive G-quadruplex formation.

机构信息

Key Laboratory of Analytical Chemistry for Biology and Medicine, Ministry of Education, College of Chemistry & Molecular Sciences, Wuhan University, Wuhan 430072, PR China.

出版信息

Talanta. 2013 Sep 30;114:138-42. doi: 10.1016/j.talanta.2013.04.003. Epub 2013 Apr 12.

Abstract

A facile and label-free assay with label-free molecular beacons (MBs) and fluorescent dye N-methyl mesoporphyrin IX (NMM) was developed for the detection of specific single-stranded DNA sequences. It was demonstrated by a reverse transcription oligonucleotide sequence (target DNA, 20 bases) of RNA fragment of human immunodeficiency virus (HIV) as model systems. In the absence of target DNA, the MBs were in the stem-closed form, the G-quadruplex structure could not form and the fluorescence signal of NMM was very low. In the presence of target DNA the MBs turned "Off" to "On", thus promoting the formation of G-quadruplex which could greatly enhance the fluorescence of NMM. This biosensor was simple in design, fast in operation, and more convenient and promising than other methods. It took less than 30 min to finish and its detection limit was 1.4 nM. No sophisticated experimental techniques or chemical modification for DNA sequences were required. This new approach could be widely applied to sensitive and selective nucleic acids detection.

摘要

一种简单且无需标记的测定法,使用无标记分子信标(MBs)和荧光染料 N-甲基甲川叶绿素 IX(NMM),用于检测特定的单链 DNA 序列。该测定法以人类免疫缺陷病毒(HIV)RNA 片段的逆转录寡核苷酸序列(靶 DNA,20 个碱基)作为模型系统进行了演示。在不存在靶 DNA 的情况下,MBs 呈茎环闭合形式,不能形成 G-四链体结构,NMM 的荧光信号非常低。在存在靶 DNA 的情况下,MBs 从“关闭”变为“开启”,从而促进 G-四链体的形成,这可以大大增强 NMM 的荧光。该生物传感器设计简单,操作快速,比其他方法更方便、更有前途。整个过程不到 30 分钟即可完成,检测限为 1.4 nM。无需对 DNA 序列进行复杂的实验技术或化学修饰。这种新方法可广泛应用于灵敏和选择性核酸检测。

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