光电流
级联
生物传感器
化学
对偶(语法数字)
纳米技术
DNA
SOS响应
抗生素
组合化学
生物系统
生物物理学
DNA损伤
光电子学
材料科学
生物化学
色谱法
生物
艺术
物理
文学类
作者
Liang Pan,Wan Huang,Can Li,Xin Li,Guosong Lai
标识
DOI:10.1016/j.aca.2023.341240
摘要
The construction of effective methods for the convenient testing of antibiotic residues in real samples has attracted considerable interest. Herein, we designed a dual cascade DNA walking amplification strategy and combined it with the controllable photocurrent regulation of a photoelectrode to develop a novel photoelectrochemical (PEC) biosensing method for antibiotic detection. The photoelectrode was prepared through the surface modification of a glassy carbon electrode with the TiO2/CdS QDs nanocomposite synthesized by an in situ hydrothermal deposition method. The strong anodic PEC response of the nanocomposite could be well inhibited by the introduction of a silver nanoclusters (Ag NCs)-labeled DNA hairpin onto its surface. Upon the target biorecognition reaction, an Mg2+-dependent DNAzyme (MNAzyme)-driven DNA walking was triggered to release another MNAzyme strand-linked streptavidin (SA) complex. As this SA complex could serve as a four-legged DNA walker, its cascade walking on the electrode surface not only released Ag NCs but also caused the linking of Rhodamine 123 with the electrode to realize the “super on” photocurrent output. By using kanamycin as the model analyte, this method showed a very wide linear range from 10 fg mL−1 to 1 ng mL−1 and a very low detection limit of 0.53 fg mL−1. Meanwhile, the simple photoelectrode preparation and the aptamer recognition-based autonomous DNA walking resulted in the convenient manipulation and excellent repeatability. These unique performances determine the great potential of the proposed method for practical applications.
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