Photothermal biosensor for HPV16 based on strand-displacement amplification and gold nanoparticles using a thermometer as readout

被引:5
|
作者
Yan, Bingyan [1 ,2 ]
Li, Min [3 ]
Luo, Fang [2 ]
Jin, XiaoYa [1 ]
Qiu, Bin [2 ]
Lin, Zhenyu [2 ]
机构
[1] Wenzhou Med Univ, Dept Infect Dis, Key Lab Diag & Controlment Dev Chron Liver Dis Zh, Affiliated Hosp 1, Wenzhou 325025, Peoples R China
[2] Fuzhou Univ, Key Lab Anal & Detect Food Safety, Coll Chem, Minist Educ,Key Lab Analyt Sci Food Safety & Biol, 2 Xue Yuan Rd, Fuzhou 350116, Fujian, Peoples R China
[3] Fujian Med Univ, Fujian Prov Hosp, Dept Gen Med, Prov Clin Med Coll 13, Fuzhou 350001, Fujian, Peoples R China
关键词
Photothermal effect; Gold nanoparticle; Strand-displacement amplification; Human papillomavirus; Thermometer; ELECTROCHEMICAL BIOSENSOR; AGGREGATION;
D O I
10.1007/s00604-022-05522-z
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Gold nanoparticles (AuNPs) in aggregated state have a strong near infrared region (NIR) absorption and the causes a much stronger photothermal effect than that of the dispersed AuNPs. Strand-displacement amplification (SDA) can produce large amount of single-stranded DNA (ssDNA), which in turn effectively prevent AuNPs from aggregation. In this study, these characteristics had been applied to design a photothermal biosensor for human papilloma virus (HPV and HPV16 were chosen as model target) detection. In the absence of HPV16, AuNPs was in the aggregated state and large temperature rise can be detected after the irradiation by 808 nm laser. The presence of HPV16 triggers the SDA reaction with the help of Bst DNA polymerase and Nt.BstNBI nicking endonuclease resulting in the production of large amounts of ssDNA; this protects unmodified AuNPs from salt-induced aggregation. Therefore, AuNPs was in a dispersed state and the temperature change was not significant after the irradiation of 808 nm laser. The difference of the temperature changing can be applied for the quantitative detection of HPV16 using a thermometer as readout. The linear response range is 1.0 fM similar to 50 pM with a detection limit of 0.3 fM. The proposed method has been applied to detect HPV16 in clinical cervical sample and is competent for clinical analysis.
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收藏
页数:9
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