State Key Laboratory Base of Eco-chemical Engineering, College of Chemistry and Molecular Engineering, Qingdao University of Science and Technology , Qingdao, Shandong 266042, P. R. China.
Anal Chem. 2014 Jan 7;86(1):336-9. doi: 10.1021/ac4038043. Epub 2013 Dec 18.
MicroRNAs (miRNAs) are promising targets for disease diagnosis. However, miRNA detection requires rapid, sensitive, and selective detection to be effective as a diagnostic tool. Herein, a miRNA-initiated exponential strand-displacement amplification (SDA) assay was reported. With the Klenow fragment, nicking enzyme Nt.AlwI, and two primers, the miRNA target can trigger two cycles of nicking, polymerization, and displacement reactions. These reaction cycles amplified the target miRNA exponentially and generated dsDNAs detectable with SYBR Green I in real-time PCR. As low as 16 zmol of the target miRNA was detected by this one-pot assay within 90 min, and the dynamic range spanned over 9 orders of magnitude. Negligible impact from the complex biological matrix was observed on the amplification reaction, indicating the assay's capability to directly detect miRNAs in biofluids.
微小 RNA(miRNAs)是疾病诊断有前途的靶点。然而,miRNA 的检测需要快速、敏感和选择性的检测,才能有效地作为一种诊断工具。在此,报告了一种 miRNA 引发的指数链置换扩增(SDA)检测法。利用 Klenow 片段、切口酶 Nt.AlwI 和两条引物,miRNA 靶标可以触发两个循环的切口、聚合和置换反应。这些反应循环使靶 miRNA 指数级扩增,并在实时 PCR 中生成可检测的双链 DNA。通过这种一锅法,在 90 分钟内可以检测到低至 16 zmol 的靶 miRNA,其动态范围跨越 9 个数量级。复杂的生物基质对扩增反应的影响可以忽略不计,表明该检测法能够直接检测生物流体中的 miRNAs。