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多重单分子 DNA 条形码技术:基于寡核苷酸连接分析。

Multiplex Single-Molecule DNA Barcoding Using an Oligonucleotide Ligation Assay.

机构信息

Kavli Institute of NanoScience, Department of BioNanoScience, Delft University of Technology, Delft, The Netherlands.

Kavli Institute of NanoScience, Department of BioNanoScience, Delft University of Technology, Delft, The Netherlands.

出版信息

Biophys J. 2018 Sep 18;115(6):957-967. doi: 10.1016/j.bpj.2018.08.013. Epub 2018 Aug 18.

Abstract

Detection of specific nucleic acid sequences is invaluable in biological studies such as genetic disease diagnostics and genome profiling. Here, we developed a highly sensitive and specific detection method that combines an advanced oligonucleotide ligation assay with multicolor single-molecule fluorescence. We demonstrated that under our experimental conditions, 7-nucleotide long DNA barcodes have the optimal short length to ascertain specificity while being long enough for sufficient ligation. Using four spectrally separated fluorophores to label DNA barcodes, we simultaneously distinguished four DNA target sequences differing by only a single nucleotide. Our single-molecule approach will allow for accurate identification of low-abundance molecules without the need for target DNA preamplification.

摘要

在生物研究中,如遗传疾病诊断和基因组分析,检测特定的核酸序列是非常有价值的。在这里,我们开发了一种高度敏感和特异性的检测方法,将先进的寡核苷酸连接测定法与多色单分子荧光结合起来。我们证明,在我们的实验条件下,7 个核苷酸长的 DNA 条码具有最佳的短长度,以确保特异性,同时也足够长以进行充分的连接。我们使用四种光谱分离的荧光染料标记 DNA 条码,能够同时区分仅相差一个核苷酸的四个 DNA 靶序列。我们的单分子方法将允许在不需要靶 DNA 预扩增的情况下,准确识别低丰度分子。

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