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基于生物催化加速的 N-(氨丁基)-N-(乙基异鲁米诺)/溶解 O 体系的电致化学发光用于 microRNA 检测。

Electrochemiluminescence from a biocatalysis accelerated N-(aminobutyl)-N-(ethylisoluminol)/dissolved O system for microRNA detection.

机构信息

Key Laboratory of Luminescent and Real-Time Analytical Chemistry (Southwest University), Ministry of Education, College of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China.

出版信息

Mikrochim Acta. 2021 May 27;188(6):205. doi: 10.1007/s00604-021-04854-6.

Abstract

A kind of biocatalyst, laccase, has been employed as a biocompatible coreactant accelerator to efficiently catalyze coreactant (dissolved O) for generating high local concentration of superoxide radical (O), acquiring high-intense electrochemiluminescence (ECL) emission of ABEI (N-(aminobutyl)-N-(ethylisoluminol))/dissolved O system. Furthermore, a modified strand displacement reaction with excellent amplification efficiency was constructed by replacing traditional single strand DNA to the hairpin DNA as template for triggering the immobilization of more signal probes. As a result, the biosensor for microRNA-21 determination has preeminent selectivity and favorable sensitivity with detection limit down to 80.8 aM. Significantly, the devised strategy has blazed a new path for seeking more coreaction accelerators with splendid biocompatibility thus promoting the application of ternary ECL systems in biological analysis and clinical diagnosis.

摘要

一种生物催化剂,漆酶,被用作生物相容性的共反应加速剂,以有效地催化共反应剂(溶解氧),生成超氧自由基(O)的高局部浓度,获得 ABEI(N-(氨基丁基)-N-(乙基异鲁米诺)/溶解 O 体系的高强度电化学发光(ECL)发射。此外,通过用发夹 DNA 代替传统的单链 DNA 作为模板,构建了一种具有优异放大效率的改良链置换反应,以触发更多信号探针的固定化。结果,用于 microRNA-21 测定的生物传感器具有卓越的选择性和良好的灵敏度,检测限低至 80.8 aM。值得注意的是,该设计策略为寻找更多具有出色生物相容性的共反应加速剂开辟了新途径,从而促进了三元 ECL 系统在生物分析和临床诊断中的应用。

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