School of Laboratory Medicine, Hubei University of Chinese Medicine , 1 Huangjia Lake West Road, Wuhan, Hubei 430065, China.
Anal Chem. 2017 May 16;89(10):5511-5518. doi: 10.1021/acs.analchem.7b00487. Epub 2017 Apr 28.
Here, we demonstrate a phosphorodiamidate morpholino oligos (PMO)-functionalized nanochannel biosensor for label-free detection of microRNAs (miRNAs) with ultrasensitivity and high sequence specificity. PMO, as a capture probe, was covalently anchored on the nanochannel surface. Because of the neutral character and high sequence-specific affinity of PMO, hybridization efficiency between PMO and miRNAs was enhanced, thus largely decreasing background signals and highly improving the detection specificity and sensitivity. The miRNAs detection was realized through observing the change of surface charge density when PMO/miRNAs hybridization occurred. Not only could the developed biosensor specifically discriminate complementary miRNAs (Let-7b) from noncomplementary miRNAs (miR-21) and one-base mismatched miRNAs (Let-7c), but also it could detect target miRNAs in serum samples. In addition, this nanochannel-based biosensor attained a reliable limit of detection down to 1 fM in PBS and 10 fM in serum sample, respectively. It is expected that such a new method will benefit miRNA detection in clinical diagnosis.
在这里,我们展示了一种基于磷酰二胺吗啉寡聚物 (PMO) 的纳米通道生物传感器,用于超灵敏和高序列特异性地无标记检测 microRNAs (miRNAs)。PMO 作为捕获探针被共价固定在纳米通道表面。由于 PMO 的中性特征和高序列特异性亲和力,PMO 与 miRNAs 之间的杂交效率得到增强,从而大大降低了背景信号,高度提高了检测的特异性和灵敏度。通过观察 PMO/miRNAs 杂交时表面电荷密度的变化来实现 miRNAs 的检测。该生物传感器不仅可以特异性地区分互补的 miRNAs (Let-7b) 与非互补的 miRNAs (miR-21) 和一个碱基错配的 miRNAs (Let-7c),还可以检测血清样本中的靶标 miRNAs。此外,这种基于纳米通道的生物传感器在 PBS 中的可靠检测限低至 1 fM,在血清样本中的可靠检测限低至 10 fM。预计这种新方法将有益于临床诊断中的 miRNA 检测。