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实时、无标记等温固相扩增/检测(ISAD)装置,用于快速检测癌症中的遗传改变。

Real-time, label-free isothermal solid-phase amplification/detection (ISAD) device for rapid detection of genetic alteration in cancers.

机构信息

Institute of Microelectronics, A*STAR (Agency for Science, Technology and Research), 11 Science Park Road, Singapore Science Park II, Singapore 117685.

出版信息

Lab Chip. 2013 Jun 7;13(11):2106-14. doi: 10.1039/c3lc50129a.

Abstract

Here, we first present an isothermal solid-phase amplification/detection (ISAD) technique for the detection of single-point mutations that can be performed without labelling in real-time by utilizing both silicon microring-based solid-phase amplification and isothermal recombinase polymerase amplification (RPA). The ISAD technique was performed on a silicon microring device with a plastic chamber containing 10 μL of the reaction mixture, and characterized with an assay for the detection of the HRAS (Harvey RAS) gene single-point mutation. For the solid-phase amplification, the primer of the gene was directly attached to the surface of the device via an amine modification reaction. The amplified DNA was detected, without a label, by measuring the optical wavelength shift of the silicon microring resonator during the reaction. We demonstrated that the sensitivity of the ISAD technique was 100-times higher than that of RPA and conventional PCR methods. Moreover, this technique can be used to distinguish a single-point mutation of the HRAS gene via target amplification. This novel DNA amplification/detection technique will be useful for the detection of sequence alterations such as mutations and single-nucleotide polymorphisms as DNA biomarkers in human diseases.

摘要

在这里,我们首先提出了一种等温固相扩增/检测(ISAD)技术,用于检测单点突变,该技术可通过利用基于硅微环的固相扩增和等温重组酶聚合酶扩增(RPA)实时进行无标记检测。ISAD 技术在一个带有容纳 10 μL 反应混合物的塑料腔的硅微环设备上进行,并对 Harvey RAS(HRAS)基因单点突变的检测进行了分析。对于固相扩增,通过胺修饰反应将基因的引物直接连接到设备表面。通过在反应过程中测量硅微环谐振器的光学波长位移,无需标记即可检测到扩增的 DNA。我们证明,ISAD 技术的灵敏度比 RPA 和常规 PCR 方法高 100 倍。此外,该技术可用于通过目标扩增来区分 HRAS 基因的单点突变。这种新型 DNA 扩增/检测技术将有助于检测人类疾病中作为 DNA 生物标志物的突变和单核苷酸多态性等序列改变。

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