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用于可视化检测转基因生物的基于纳米颗粒的DNA生物传感器。

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

作者信息

Kalogianni Despina P, Koraki Theodora, Christopoulos Theodore K, Ioannou Penelope C

机构信息

Department of Chemistry, University of Patras, Patras 26500, Greece.

出版信息

Biosens Bioelectron. 2006 Jan 15;21(7):1069-76. doi: 10.1016/j.bios.2005.04.016. Epub 2005 Jun 2.

Abstract

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 (7min) 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 0.16nM. 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.

摘要

虽然通过检测外源DNA或新蛋白均可实现对转基因生物(GMO)的原料和食品进行筛选,但由于DNA在食品加工过程中具有更高的稳定性,因此它是首选的分析物。由于对转基因生物检测的快速可靠方法的需求不断增长,DNA生物传感器的开发变得越来越重要。我们报道了首个采用干试剂试纸条形式的DNA生物传感器,可在数分钟内通过杂交实现对转基因生物相关序列的可视化检测和确认。该传感器为一次性使用,无需特殊仪器。它可检测大多数转基因植物中存在的35S启动子和胭脂碱合酶(NOS)终止子序列。目标序列通过聚合酶链反应(PCR)进行扩增,并与带有寡聚(dA)尾的探针杂交(7分钟)。将生物素化产物应用于传感器,然后浸入适当的缓冲液中。缓冲液的迁移使与寡聚(dT)偶联的金纳米颗粒重新水化,后者与寡聚(dA)尾杂交。杂交产物在传感器的测试区被固定化的链霉亲和素捕获,由于纳米颗粒的积累而产生特征性的红线。过量的纳米颗粒偶联物在对照区被固定化的寡聚(dA)链捕获。扩增后的35S或NOS DNA在0.16nM时可被检测到。分别经过35个和40个扩增循环后,可清晰检测到含有0.1%转基因生物含量的大豆粉标准参考物质中的35S和NOS序列。该传感器还应用于来自各种来源的实际样品。

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