A fluorometric aptamer nanoprobe for alpha-fetoprotein by exploiting the FRET between 5-carboxyfluorescein and palladium nanoparticles

被引:51
作者
Li, Guiyin [1 ]
Zeng, Junxiang [1 ]
Liu, Huiling [1 ]
Ding, Ping [2 ]
Liang, Jintao [1 ]
Nie, Xinmin [3 ]
Zhou, Zhide [1 ]
机构
[1] Guilin Univ Elect Technol, Sch Life & Environm Sci, Guilin 541004, Guangxi, Peoples R China
[2] Cent South Univ, Xiang Ya Sch Publ Hlth, Changsha 410078, Hunan, Peoples R China
[3] Cent South Univ, Xiangya Hosp 3, Clin Lab, Changsha 410013, Hunan, Peoples R China
关键词
Fluorescence resonance energy transfer; Alpha-fetoprotein; Palladium nanoparticles; Aptamer; IMMUNE SENSOR; TUMOR-MARKERS; APTASENSOR; GRAPHENE;
D O I
10.1007/s00604-019-3403-z
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Alpha-fetoprotein (AFP) is a reliable clinical marker of hepatocellular carcinoma (HCC). A highly sensitive fluorometric aptamer nanoprobe is described for AFP detection. It is based on fluorescence resonance energy transfer (FRET) between AFP aptamer labelled with 5-carboxyfluorescein (FAM) and palladium nanoparticles (PdNPs). The PdNPs quench the green fluorescence of the FAM-AFP aptamer via interactions between nitrogen functional groups of the AFP aptamer and PdNPs. When AFP was introduced into the FAM-AFP aptamer-PdNPs FRET system, the AFP aptamer preferentially combines with AFP. This results in a conformational change and weakens the interaction between the aptamer and the PdNPs. Thus, the fluorescence of FAM recovers. The fluorescence recovery of FAM increases linearly in the 5.0-150 ng center dot mL(-1) AFP concentration range and has a 1.4 ng center dot mL(-1) detection limit. The assay was applied to the analysis of spiked diluted human serum. The recovery values ranged from 98.3 to 112.9%, with relative standard deviations of <1.1%. This biosensing strategy provides a reliable and ultrasensitive protocol for the quantification of biomarkers with relevant antigens and aptamers.
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页数:9
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