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Non-Enzymatic Detection of Bacterial Genomic DNA Using the Bio-Barcode Assay

机译:使用生物条形码检测技术对细菌基因组DNA进行非酶检测

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摘要

The detection of bacterial genomic DNA through a non-enzymatic nanomaterials based amplification method, the bio-barcode assay, is reported. The assay utilizes oligonucleotide functionalized magnetic microparticles to capture the target of interest from the sample. A critical step in the new assay involves the use of blocking oligonucleotides during heat denaturation of the double stranded DNA. These blockers bind to specific regions of the target DNA upon cooling, and prevent the duplex DNA from re-hybridizing, which allows the particle probes to bind. Following target isolation using the magnetic particles, oligonucleotide functionalized gold nanoparticles act as target recognition agents. The oligonucleotides on the nanoparticle (barcodes) act as amplification surrogates. The barcodes are then detected using the Scanometric method. The limit of detection for this assay was determined to be 2.5 femtomolar, and this is the first demonstration of a barcode type assay for the detection of double stranded, genomic DNA.
机译:报道了通过基于非酶纳米材料的扩增方法,即生物条形码检测法,检测细菌基因组DNA。该测定法利用寡核苷酸官能化的磁性微粒从样品中捕获目标靶标。新测定的关键步骤涉及在双链DNA热变性过程中使用封闭寡核苷酸。这些阻断剂在冷却后与靶DNA的特定区域结合,并防止双链体DNA再次杂交,从而使颗粒探针结合。使用磁性颗粒分离靶标后,寡核苷酸官能化的金纳米颗粒充当靶标识别剂。纳米颗粒上的寡核苷酸(条形码)充当扩增替代物。然后使用Scanometric方法检测条形码。该检测的检测极限被确定为2.5飞摩尔,这是用于检测双链基因组DNA的条形码类型检测的首次证明。

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