Cascade signal amplifying strategy for ultrasensitive detection of tumor biomarker by DNAzyme cleaving mediated HCR

被引:19
|
作者
Chen, Huinan [1 ]
Song, Jingyao [1 ]
Li, Yuanyuan [1 ]
Deng, Dongmei [1 ]
Song, Yuchen [1 ]
Zhu, Xiaoli [2 ]
Luo, Liqiang [1 ]
机构
[1] Shanghai Univ, Coll Sci, Shanghai 200444, Peoples R China
[2] Tongji Univ, Shanghai Peoples Hosp 10, Sch Med, Dept Clin Lab Med, Shanghai 200072, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Biomarker; AFP; DNAzyme; Hybridization chain reaction; Immunosensor; HEPATOCELLULAR-CARCINOMA; ALPHA-FETOPROTEIN;
D O I
10.1016/j.snb.2024.136466
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Tumor biomarkers are a kind of important biomolecules for aiding cancer diagnosis and assessing tumor efficacy, among which alpha-fetoprotein (AFP) is a crucial tumor biomarker for the early diagnosis of hepatocellular carcinoma. In this study, a novel cascade signal amplifying strategy was designed for the ultrasensitive detection of AFP by DNAzyme cleaving-mediated hybridization chain reaction (HCR). The primary antibody was immobilized on the Au nanoparticles modified glassy carbon electrode, which subsequently captured AFP and the secondary antibody. Then, streptavidin was combined with the biotin-modified secondary antibody and Cu2+specific DNAzyme. When Cu2+ was present, the substrate strand of the DNAzyme would cleave and produce an ssDNA end. Finally, HCR was triggered to form long double-stranded DNA on the electrode, which would greatly inhibit the charge transfer at the electrode/solution interface. Therefore, the DNAzyme cleaving-mediated HCR strategy can be applied as cascade signal amplification for the ultrasensitive electrochemical determination of tumor biomarker AFP. Under optimal conditions, the immunosensor exhibits a broad linear range of 0.001-100 ng center dot mL- 1 (R2 = 0.990) and a low detection limit of 15.8 fg center dot mL- 1. The proposed sensor displays high sensitivity and selectivity for AFP detection, which can be employed as a universal sensing platform in clinical diagnostics.
引用
收藏
页数:9
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