Rapid and Wash-Free Time-Gated FRET Histamine Assays Using Antibodies and Aptamers

被引:15
作者
Fu, Hui-Jun [1 ,2 ,3 ]
Su, Ruifang [1 ,2 ,4 ,5 ]
Luo, Lin [3 ]
Chen, Zi-Jian [3 ]
Sorensen, Thomas Just [4 ,5 ]
Hildebrandt, Niko [1 ,2 ,6 ,7 ]
Xu, Zhen-Lin [3 ]
机构
[1] Normandie Univ, Univ Rouen Normandie, CNRS,INSA,nanoFRETcom, Lab COBRA Chim Organ Bioorgan Reactivite & Anal U, F-76000 Rouen, France
[2] Normandie Univ, Univ Rouen Normandie, CNRS,INSA, FR3038, F-76000 Rouen, France
[3] South China Agr Univ, Guangdong Prov Key Lab Food Qual & Safety, Guangdong Lab Lingnan Modern Agr, Guangzhou 510642, Peoples R China
[4] Univ Copenhagen, Nanosci Ctr, DK-2100 Copenhagen, Denmark
[5] Univ Copenhagen, Dept Chem, DK-2100 Copenhagen, Denmark
[6] Seoul Natl Univ, Dept Chem, Seoul 08826, South Korea
[7] Univ Paris Saclay, F-91405 Orsay, France
基金
新加坡国家研究基金会;
关键词
aptasensors; immunoassays; food testing; fluorescence; Fo?rster resonance energy transfer; RESONANCE ENERGY-TRANSFER; IMMUNOASSAY; TYRAMINE;
D O I
10.1021/acssensors.2c00085
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Histamine (HA) is an indicator of food freshness and quality. However, high concentrations of HA can cause food poisoning. Simple, rapid, sensitive, and specificquantification can enable efficient screening of HA in food and beverages. However,conventional assays are complicated and time-consuming, as they require multiple incubation,washing, and separation steps. Here, we demonstrate that time-gated Fo??rster resonance energytransfer (TG-FRET) between terbium (Tb) complexes and organic dyes can be implementedin both immunosensors and aptasensors for simple HA quantification using a rapid, single-step,mix-and-measure assay format. Both biosensors could quantify HA at concentrations relevant infood poisoning with limits of detection of 0.19 mu g/mL and 0.03 mu g/mL, respectively. Excellentspecificity was documented against the structurally similar food components tryptamine andL-histidine. Direct applicability of the TG-FRET assays was demonstrated by quantifying HA inspikedfish and wine samples with both excellent concentration recovery and agreement withconventional multistep enzyme-linked immunosorbent assays (ELISAs). Our results show thatthe simplicity and rapidity of TG-FRET assays do not compromise sensitivity, specificity, andreliability, and both immunosensors and aptasensors have a strong potential for their implementation in advanced food safety screening
引用
收藏
页码:1113 / 1121
页数:9
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