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基于 DNA-蛋白质相互作用和外切酶 III 辅助目标循环扩增的灵敏光电化学测定 microRNA-21 的 AnCuInS 光阴极。

An CuInS photocathode for the sensitive photoelectrochemical determination of microRNA-21 based on DNA-protein interaction and exonuclease III assisted target recycling amplification.

机构信息

Key Laboratory of Analytical Chemistry for Life Science in Universities of Shandong, Qingdao University of Science and Technology, Qingdao, 266042, People's Republic of China.

Key Laboratory of Biochemical Analysis, Qingdao University of Science and Technology, Qingdao, 266042, People's Republic of China.

出版信息

Mikrochim Acta. 2019 Oct 12;186(11):692. doi: 10.1007/s00604-019-3804-z.

Abstract

A photocathode is described for the determination of microRNA-21 by using CuInS as an active photocathode material. Exonuclease III assisted target recycling amplification was employed to enhance the detection sensitivity. The TATA-binding protein (TBP) was applied to enhance steric hindrance which decreases the photoelectrochemical intensity. This strategy is designed by combining the anti-interference photocathode material, enzyme assisted target recycling amplification and TBP induced signal off, showing remarkable amplification efficiency. Under the optimized conditions, the detection limit for microRNA-21 is as low as 0.47 fM, and a linear range was got from 1.0 × 10 M to 1.0 × 10 M. Graphical abstract Schematic representation of sensitive photoelectrochemical detection of microRNA-21.CuInS is used as an active photocathode material. Combined Exonuclease III assisted target recycling amplification and TATA-binding protein decreased of photoelectrochemical intensity, the detection limit was 0.47 fM with good selectivity. (miR-21: microRNA-21; CS: chitosan).

摘要

一种用于测定 microRNA-21 的光电阴极,其特征在于,CuInS 用作活性光电阴极材料。采用外切核酸酶 III 辅助的靶标循环放大来提高检测灵敏度。TATA 结合蛋白(TBP)用于增强空间位阻,从而降低光电化学强度。该策略通过结合抗干扰光电阴极材料、酶辅助的靶标循环放大和 TBP 诱导的信号关闭来设计,显示出显著的放大效率。在优化条件下,microRNA-21 的检测限低至 0.47 fM,线性范围为 1.0×10-15 M 至 1.0×10-11 M。

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