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高度快速免扩增定量DNA成像检测法

Highly rapid amplification-free and quantitative DNA imaging assay.

作者信息

Klamp Tobias, Camps Marta, Nieto Benjamin, Guasch Francesc, Ranasinghe Rohan T, Wiedemann Jens, Petrášek Zdeněk, Schwille Petra, Klenerman David, Sauer Markus

机构信息

Department of Biotechnology & Biophysics, Biocenter, Julius-Maximilians-University Würzburg, Am Hubland, 97074 Würzburg, Germany.

出版信息

Sci Rep. 2013;3:1852. doi: 10.1038/srep01852.

Abstract

There is an urgent need for rapid and highly sensitive detection of pathogen-derived DNA in a point-of-care (POC) device for diagnostics in hospitals and clinics. This device needs to work in a 'sample-in-result-out' mode with minimum number of steps so that it can be completely integrated into a cheap and simple instrument. We have developed a method that directly detects unamplified DNA, and demonstrate its sensitivity on realistically sized 5 kbp target DNA fragments of Micrococcus luteus in small sample volumes of 20 μL. The assay consists of capturing and accumulating of target DNA on magnetic beads with specific capture oligonucleotides, hybridization of complementary fluorescently labeled detection oligonucleotides, and fluorescence imaging on a miniaturized wide-field fluorescence microscope. Our simple method delivers results in less than 20 minutes with a limit of detection (LOD) of ~5 pM and a linear detection range spanning three orders of magnitude.

摘要

迫切需要在医院和诊所的即时护理(POC)诊断设备中对病原体衍生的DNA进行快速且高度灵敏的检测。该设备需要以最少的步骤在“样本进-结果出”模式下工作,以便能够完全集成到廉价且简单的仪器中。我们开发了一种直接检测未扩增DNA的方法,并在20μL小样本体积中,针对实际大小的5kbp藤黄微球菌靶DNA片段展示了其灵敏度。该检测方法包括用特定的捕获寡核苷酸在磁珠上捕获和积累靶DNA、互补荧光标记检测寡核苷酸的杂交以及在小型化宽视野荧光显微镜上进行荧光成像。我们的简单方法在不到20分钟内得出结果,检测限(LOD)约为5pM,线性检测范围跨越三个数量级。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cca3/3655336/204ec3fa191e/srep01852-f1.jpg

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