Department of Chemistry, University of California, Riverside, Riverside, CA, 92521, USA.
Anal Bioanal Chem. 2020 Apr;412(11):2399-2412. doi: 10.1007/s00216-020-02496-w. Epub 2020 Feb 19.
The detection of circulating miRNA through isothermal amplification wields many attractive advantages over traditional methods, such as reverse transcription RT-qPCR. However, it is challenging to control the background signal produced in the absence of target, which severely hampers applications of such methods for detecting low abundance targets in complex biological samples. In the present work, we employed both the cobalt oxyhydroxide (CoOOH) nanoflakes and the chemical modification of hexanediol to block non-specific template elongation in exponential amplification reaction (EXPAR). Adsorption by the CoOOH nanoflakes and the hexanediol modification at the 3' end effectively prevented no-target polymerization on the template itself and thus greatly improved the performance of EXPAR, detecting as low as 10 aM of several miRNA targets, including miR-16, miR-21, and miR-122, with the fluorescent DNA staining dye of SYBR Gold™. Little to no cross-reactivity was observed from the interfering strands present in 10-fold excess. Besides contributing to background reduction, the CoOOH nanoflakes strongly adsorbed nucleic acids and isolated them from a complex sample matrix, thus permitting successful detection of the target miRNA in the serum. We expect that simple but sensitive template-blocking EXPAR could be a valuable tool to help with the discovery and validation of miRNA markers in biospecimens. Graphical abstract.
通过等温扩增检测循环 miRNA 相对于传统方法(如反转录 RT-qPCR)具有许多吸引人的优势。然而,在没有靶标的情况下控制背景信号的产生具有挑战性,这严重阻碍了此类方法在复杂生物样品中检测低丰度靶标中的应用。在本工作中,我们同时采用了钴氢氧化物(CoOOH)纳米片和己二醇的化学修饰来阻止指数扩增反应(EXPAR)中模板的非特异性延伸。CoOOH 纳米片的吸附和 3'端的己二醇修饰有效地阻止了模板本身上无靶标聚合,从而极大地提高了 EXPAR 的性能,能够检测到低至 10 aM 的几种 miRNA 靶标,包括 miR-16、miR-21 和 miR-122,使用荧光 DNA 染色染料 SYBR Gold™。即使在 10 倍过量的干扰链存在的情况下,也几乎没有观察到交叉反应。除了有助于减少背景信号之外,CoOOH 纳米片还能强烈吸附核酸并将其与复杂的样品基质分离,从而能够成功检测血清中的靶标 miRNA。我们预计,简单但灵敏的模板阻断 EXPAR 可能成为帮助在生物样本中发现和验证 miRNA 标记的有价值的工具。