| Literature DB >> 31605242 |
Chao Liu1,2,3,4,5,6, Li Zhao1,2,3,4,5,6, Dongxia Liang1,2,3,4,5,6, Xiaoru Zhang1,2,3,4,5,6, Weiling Song7,8,9,10,11,12.
Abstract
A photocathode is described for the determination of microRNA-21 by using CuInS2 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 × 10-15 M to 1.0 × 10-6 M. Graphical abstract Schematic representation of sensitive photoelectrochemical detection of microRNA-21.CuInS2 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).Entities:
Keywords: Aptamer; Electrode; Nanoflowers; Photoelectrochemistry; Photoresponse; TATA-binding protein
Mesh:
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Year: 2019 PMID: 31605242 DOI: 10.1007/s00604-019-3804-z
Source DB: PubMed Journal: Mikrochim Acta ISSN: 0026-3672 Impact factor: 5.833