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定量检测未经扩增或标记的少于十个拷贝的 DNA 生物标志物。

Quantification of Fewer than Ten Copies of a DNA Biomarker without Amplification or Labeling.

机构信息

Nanogea Inc. , 6162 Bristol Parkway, Culver City, California 90230, United States.

出版信息

J Am Chem Soc. 2016 Jun 8;138(22):7075-81. doi: 10.1021/jacs.6b02791. Epub 2016 May 26.

Abstract

Polymerase chain reaction (PCR) is a highly sensitive diagnosis technique for detection of nucleic acids and for monitoring residual disease; however, PCR can be unreliable for samples containing very few target molecules. Here, we describe a quantification method, using force-distance (FD) curve based atomic force microscopy (AFM) to detect a target DNA bound to small (1.4-1.9 μm diameter) probe DNA spots, allowing mapping of entire spots to nanometer resolution. Using a synthetic BCR-ABL fusion gene sequence target, we examined samples containing between one and 10 target copies. A high degree of correlation (r(2) = 0.994) between numbers of target copies and detected probe clusters was observed, and the approach could detect the BCR-ABL biomarker when only a single copy was present, although multiple screens were required. Our results clearly demonstrate that FD curve-based imaging is suitable for quantitative analysis of fewer than 10 copies of DNA biomarkers without amplification, modification, or labeling.

摘要

聚合酶链式反应(PCR)是一种高度敏感的核酸检测和残留疾病监测技术;然而,对于包含非常少量靶分子的样本,PCR 可能不可靠。在这里,我们描述了一种定量方法,使用基于力-距离(FD)曲线的原子力显微镜(AFM)来检测与小(1.4-1.9 μm 直径)探针 DNA 点结合的靶 DNA,允许将整个斑点映射到纳米分辨率。使用合成的 BCR-ABL 融合基因序列靶标,我们检查了包含 1 到 10 个靶标拷贝的样本。观察到靶标拷贝数与检测到的探针簇之间具有高度相关性(r(2) = 0.994),并且即使需要多次筛选,该方法也可以检测到单个拷贝存在的 BCR-ABL 生物标志物。我们的结果清楚地表明,FD 曲线成像适合于在不扩增、修饰或标记的情况下对少于 10 个拷贝的 DNA 生物标志物进行定量分析。

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