Nanoparticle-based DNA biosensor for visual detection of genetically modified organisms

被引:74
作者
Kalogianni, DP
Koraki, T
Christopoulos, TK [1 ]
Ioannou, PC
机构
[1] Univ Patras, Dept Chem, Patras 26500, Greece
[2] Eugene SA, Athens 15772, Greece
[3] Fdn Res & Technol Hellas, ICEHT, FORTH, Inst Chem Engn & High Temp Chem Proc, Patras 26504, Greece
[4] Univ Athens, Dept Chem, GR-15771 Athens, Greece
关键词
GMO; genetically modified organisms; nanoparticles; DNA biosensor; DNA hybridization;
D O I
10.1016/j.bios.2005.04.016
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Although screening of raw ingredients and food products for genetically modified organisms (GMO) may be accomplished by detecting either the exogenous DNA or the novel protein, DNA is the preferred analyte because of its superior stability during food processing. The development of DNA biosensors is of increasing importance due to the growing demand for rapid and reliable methods for GMO detection. We report the first DNA biosensor in a dry-reagent dipstick configuration for visual detection and confirmation of GMO-related sequences by hybridization within minutes. The sensor is disposable and does not require special instrumentation. It detects the 35S promoter and nopaline synthase (NOS) terminator sequences that are present in the majority of transgenic plants. The target sequences are amplified by the polymerase chain reaction (PCR) and hybridized (7 min) with probes bearing oligo(dA) tail. The biotinylated product is applied to the sensor followed by immersion in the appropriate buffer. Migration of the buffer rehydrates gold nanoparticles conjugated to oligo(dT), which hybridize with the oligo(dA) tails. The hybrids are captured by immobilized streptavidin at the test zone of the sensor giving a characteristic red line due to the accumulation of the nanoparticles. The excess of nanoparticle conjugates are captured at the control zone by immobilized oligo(dA) strands. Amplified 35S or NOS DNA is detectable at 0.16 nM. Soybean powder certified reference material with 0.1% GMO content is clearly detectable after 35 and 40 amplification cycles for 35S and NOS sequence, respectively. The sensor was also applied to real samples from various sources. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1069 / 1076
页数:8
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