Zahid Osama K, Wang Fanny, Ruzicka Jan A, Taylor Ethan W, Hall Adam R
Virginia Tech-Wake Forest University School of Biomedical Engineering and Sciences, Wake Forest University School of Medicine , Winston-Salem, North Carolina 27101, United States.
Joint School of Nanoscience and Nanoengineering, University of North Carolina at Greensboro , Greensboro, North Carolina 27401, United States.
Nano Lett. 2016 Mar 9;16(3):2033-9. doi: 10.1021/acs.nanolett.6b00001. Epub 2016 Feb 2.
The detection and quantification of short nucleic acid sequences has many potential applications in studying biological processes, monitoring disease initiation and progression, and evaluating environmental systems, but is challenging by nature. We present here an assay based on the solid-state nanopore platform for the identification of specific sequences in solution. We demonstrate that hybridization of a target nucleic acid with a synthetic probe molecule enables discrimination between duplex and single-stranded molecules with high efficacy. Our approach requires limited preparation of samples and yields an unambiguous translocation event rate enhancement that can be used to determine the presence and abundance of a single sequence within a background of nontarget oligonucleotides.
短核酸序列的检测和定量在研究生物过程、监测疾病的发生和发展以及评估环境系统等方面具有许多潜在应用,但本质上具有挑战性。我们在此展示一种基于固态纳米孔平台的检测方法,用于识别溶液中的特定序列。我们证明,目标核酸与合成探针分子的杂交能够高效地区分双链和单链分子。我们的方法所需的样品制备有限,并产生明确的易位事件率增强,可用于确定非目标寡核苷酸背景中单个序列的存在和丰度。