Dipartimento di Chimica Ugo Schiff, Università degli Studi di Firenze, Sesto Fiorentino (Fi), Italy.
Anal Bioanal Chem. 2013 Jan;405(2-3):1025-34. doi: 10.1007/s00216-012-6476-7. Epub 2012 Oct 26.
MicroRNAs (miRNAs, miRs) are naturally occurring small RNAs (approximately 22 nucleotides in length) that have critical functions in a variety of biological processes, including tumorigenesis. They are an important target for detection technology for future medical diagnostics. In this paper we report an electrochemical method for miRNA detection based on paramagnetic beads and enzyme amplification. In particular, miR 222 was chosen as model sequence, because of its involvement in brain, lung, and liver cancers. The proposed bioassay is based on biotinylated DNA capture probes immobilized on streptavidin-coated paramagnetic beads. Total RNA was extracted from the cell sample, enriched for small RNA, biotinylated, and then hybridized with the capture probe on the beads. The beads were then incubated with streptavidin-alkaline phosphatase and exposed to the appropriate enzymatic substrate. The product of the enzymatic reaction was electrochemically monitored. The assay was finally tested with a compact microfluidic device which enables multiplexed analysis of eight different samples with a detection limit of 7 pmol L(-1) and RSD = 15 %. RNA samples from non-small-cell lung cancer and glioblastoma cell lines were also analyzed.
微小 RNA(miRNA,miRs)是一类长度约为 22 个核苷酸的内源性小分子 RNA,在多种生物学过程中发挥重要作用,包括肿瘤发生。它们是未来医学诊断检测技术的重要靶点。本文报道了一种基于超顺磁性珠和酶放大的电化学 miRNA 检测方法。具体来说,选择 miR-222 作为模型序列,因为它与脑癌、肺癌和肝癌有关。该生物测定法基于固定在链霉亲和素包被的超顺磁性珠上的生物素化 DNA 捕获探针。从细胞样本中提取总 RNA,富集小分子 RNA,然后进行生物素化,并与珠上的捕获探针杂交。然后将珠子与链霉亲和素-碱性磷酸酶孵育,并暴露于适当的酶底物。通过电化学监测酶反应的产物。该测定法最终在紧凑的微流控装置上进行了测试,该装置能够对 8 个不同样本进行多重分析,检测限为 7 pmol L(-1),RSD=15%。还分析了非小细胞肺癌和神经胶质瘤细胞系的 RNA 样本。