Amplified fluorescence detection of serum prostate specific antigen based on metal-dependent DNAzyme assistant nanomachine

被引:20
作者
Li, Binxiao [1 ,2 ]
Liu, Jing [2 ]
Zhou, Hong [2 ]
机构
[1] Shandong Normal Univ, Collaborat Innovat Ctr Functionalized Probes Chem, Jinan 250014, Shandong, Peoples R China
[2] Linyi Univ, Coll Chem & Chem Engn, Shandong Prov Key Lab Detect Technol Tumor Marker, Linyi 276005, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-dependent DNAzyme; Fluorescence detection; Prostate specific antigen; Magnetic beads; Cyclic amplification; RESONANCE ENERGY-TRANSFER; SIGNAL AMPLIFICATION; SENSITIVE DETECTION; GRAPHENE OXIDE; DNA; IMMUNOASSAY; BIOSENSOR; ASSAY; QUANTIFICATION; HYBRIDIZATION;
D O I
10.1016/j.aca.2017.12.041
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An amplified fluorescence biosensing strategy for serum prostate specific antigen (PSA) was developed on the basis of DNAzyme. In presence of cofactor Zn2+, Zn2+ -dependent DNAzyme could cleave the hairpin substrate probes which were dispersed in solution and generate remarkable fluorescent signal. Taking advantage of the magnetic beads as a carrier, one target protein could bring plentiful hairpin substrate probes on to the electrode through a sandwich structure (Ab(1)/PSA/biotin-Ab(2)). Moreover, during the cleavage process of as formed DNAzyme, DNAzyme did not be destroyed and could further react with other hairpin probes, then generated continuous fluorescent signal. Benefited by this amplified strategy, the limit of detection (LOD) was low to 0.05 ng mL(-1), which was much lower than our previous reports. This method could be applied to detect different protein biomarkers in serum without corresponding aptamers by changing the corresponding antibodies and thus showed a remarkable prospect in clinical application. (c) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:96 / 102
页数:7
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