Chongqing Engineering Laboratory of Nanomaterials & Sensor Technologies, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, China.
College of Biological and Chemical Engineering, Panzhihua University, Panzhihua 617000, China.
Anal Chem. 2020 Mar 3;92(5):3940-3948. doi: 10.1021/acs.analchem.9b05433. Epub 2020 Feb 19.
Here we described an effective recognition strategy using the target-triggered DNA structure transition as an affinity switch for nucleic acid detection based on the strong electrochemiluminescence (ECL) platform of 9,10-diphenylanthracene (DPA) doped perylene (Pe) microcrystals (DPA@Pe MCs). Specifically, the target-triggered rolling-circle amplification (RCA) could generate a long, single-stranded DNA with repeated G-quadruplex units, which would hinder the access of quenching probes due to the steric hindrance effects offered by the DNA structure transition. Using this effective recognition strategy, an ECL biosensor with ultrasensitive and accurate characteristics was proposed to detect microRNA-21, which showed an excellent linear response from 10 aM to 1 pM with the detection limit down to 4.14 aM. The DNA structure transition-induced affinity switch strategy offered a potential applications in clinical diagnosis analysis.
在这里,我们描述了一种有效的识别策略,该策略利用目标触发的 DNA 结构转变作为亲和开关,基于 9,10-二苯基蒽(DPA)掺杂苝(Pe)微晶体(DPA@Pe MCs)的强电化学发光(ECL)平台进行核酸检测。具体来说,目标触发的滚环扩增(RCA)可以产生具有重复 G-四链体单元的长单链 DNA,由于 DNA 结构转变提供的空间位阻效应,这会阻碍猝灭探针的进入。利用这种有效的识别策略,提出了一种具有超灵敏和准确特性的 ECL 生物传感器来检测 microRNA-21,其线性响应范围从 10 aM 到 1 pM,检测限低至 4.14 aM。DNA 结构转变诱导的亲和开关策略为临床诊断分析提供了潜在的应用。