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基于悬臂梁的光偏转分析法用于鉴别DNA单核苷酸错配

Cantilever-based optical deflection assay for discrimination of DNA single-nucleotide mismatches.

作者信息

Hansen K M, Ji H F, Wu G, Datar R, Cote R, Majumdar A, Thundat T

机构信息

Life Sciences Division, Oak Ridge National Laboratory, Tennessee 37831, USA.

出版信息

Anal Chem. 2001 Apr 1;73(7):1567-71. doi: 10.1021/ac0012748.

Abstract

Characterization of single-nucleotide polymorphisms is a major focus of current genomics research. We demonstrate the discrimination of DNA mismatches using an elegantly simple microcantilever-based optical deflection assay, without the need for external labeling. Gold-coated silicon AFM cantilevers were functionalized with thiolated 20- or 25-mer probe DNA oligonucleotides and exposed to target oligonucleotides of varying sequence in static and flow conditions. Hybridization of 10-mer complementary target oligonucleotides resulted in net positive deflection, while hybridization with targets containing one or two internal mismatches resulted in net negative deflection. Mismatched targets produced a stable and measurable signal when only a four-base pair stretch was complementary to the probe sequence. This technique is readily adaptable to a high-throughput array format and provides a distinct positive/negative signal for easy interpretation of oligonucleotide hybridization.

摘要

单核苷酸多态性的表征是当前基因组学研究的一个主要重点。我们展示了一种使用基于微悬臂梁的简单光学偏转检测方法来区分DNA错配,无需外部标记。金涂层硅原子力显微镜悬臂用硫醇化的20或25聚体探针DNA寡核苷酸进行功能化,并在静态和流动条件下暴露于不同序列的靶寡核苷酸。10聚体互补靶寡核苷酸的杂交导致净正偏转,而与含有一个或两个内部错配的靶杂交导致净负偏转。当只有四个碱基对的延伸与探针序列互补时,错配靶产生稳定且可测量的信号。该技术易于适应高通量阵列形式,并提供明显的正/负信号,便于解释寡核苷酸杂交。

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