Beyrampour-Basmenj Hanieh, Pourhassan-Moghamddam Mohammad, Nakhjavani Sattar Akbari, Faraji Naser, Alivand Mohammadreza, Zarghami Nosratollah, Talebi Mahnaz, Rahmati Mohammad, Ebrahimi-Kalan Abbas
IEEE Trans Nanobioscience. 2022 May 9;PP. doi: 10.1109/TNB.2022.3170530.
Multiple sclerosis (MS) remains a challenging disease that requires timely diagnosis. Therefore, an ultrasensitive optical biosensor based on hybridization chain reaction (HCR) was developed to detect microRNA-145 (miRNA-145) as an MS biomarker. To construct such a sensor, HCR occurred between specific hairpin probes, as MB1 contains a poly-cytosine nucleotide loop and MB2 has a poly-guanine nucleotide sticky end. By introducing miR-145 as a target sequence, long-range dsDNA polymers are formed. Then, positively charged gold nanoparticles (AuNPs) were incubated with the HCR product, which adsorbed onto the dsDNA polymers due to electrostatic adsorption. This resulted in the precipitation of the AuNPs. By incubating different concentrations of miR-145 with AuNPs, the changes in the UV-vis spectrum of the supernatant were analyzed. The proposed biosensor showed a great ability to detect miR-145 in a wide linear range from 1 pM-1 nM with an excellent detection limit (LOD) of 0.519 nM. Furthermore, the developed biosensor indicated considerable selectivity in discriminating between miR-145 and mismatched sequences. It shows high selectivity in differentiating targets. Interestingly, the proposed method was also able to detect miRNA-145 in the diluted serum samples. In conclusion, this sensing platform exhibits high selectivity and specificity for the detection of circulating microRNAs, which holds great promise for translation to routine clinical applications.
多发性硬化症(MS)仍然是一种具有挑战性的疾病,需要及时诊断。因此,开发了一种基于杂交链式反应(HCR)的超灵敏光学生物传感器,用于检测作为MS生物标志物的微小RNA-145(miRNA-145)。为构建这样一种传感器,特定发夹探针之间发生HCR,因为MB1包含一个聚胞嘧啶核苷酸环,而MB2具有一个聚鸟嘌呤核苷酸粘性末端。通过引入miR-145作为靶序列,形成长链双链DNA聚合物。然后,将带正电荷的金纳米颗粒(AuNPs)与HCR产物一起孵育,由于静电吸附,AuNPs吸附到双链DNA聚合物上。这导致AuNPs沉淀。通过将不同浓度的miR-145与AuNPs孵育,分析上清液紫外可见光谱的变化。所提出的生物传感器在1 pM至1 nM的宽线性范围内具有出色的检测miR-145的能力,检测限(LOD)低至0.519 nM。此外,所开发的生物传感器在区分miR-145与错配序列方面表现出相当高的选择性。它在区分靶标方面具有高选择性。有趣的是,所提出的方法还能够在稀释的血清样本中检测miRNA-145。总之,该传感平台在检测循环微小RNA方面表现出高选择性和特异性,在转化为常规临床应用方面具有很大前景。