State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio-Nanotechnology and Molecular Engineering of Hunan Province, Hunan University, Changsha 410082, China.
State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Key Laboratory for Bio-Nanotechnology and Molecular Engineering of Hunan Province, Hunan University, Changsha 410082, China.
Anal Chim Acta. 2017 Nov 15;993:55-62. doi: 10.1016/j.aca.2017.09.015. Epub 2017 Sep 13.
A high sensitive surface plasmon resonance (SPR) biosensor was proposed based on the gold nanoparticles-decorated molybdenum sulfide (AuNPs-MoS) for the first time. This SPR platform using the AuNPs-MoS nanocomposites as signal labels for the sensitive and facile measurement of microRNA (miRNA) was executed in only two steps. At first, the thiol-modified DNA oligonucleotide probes, including a sequence complementary to the target miRNA-141, were fixed on the Au film to identify the segment sequence of target miRNA-141. Then, the assistant DNA-linked AuNPs-MoS nanocomposites were used to combine with the other section of the miRNA-141. Performance of SPR biosensor was enhanced by taking advantage of the AuNPs-MoS nanocomposites, thus this newly presented sensing assay exhibited high sensitivity toward miRNA with a detection limit of 0.5 fM. Furthermore, the method showed high specificity, resulting in distinguishing differences among miRNA-200 family members. Especially, the assay could also be used to detect human miRNA from cancer cells, and the results were in excellent accord with the ones obtained using qRT-PCR. What is more, this presented method could be feasible for determining miRNA in 10% human serum. This assay may provide a great potential as a miRNA quantification method in complex samples, and exert significant effect on biomedical research and clinical early diagnosis.
首次提出了一种基于金纳米粒子修饰的二硫化钼(AuNPs-MoS)的高灵敏表面等离子体共振(SPR)生物传感器。该 SPR 平台使用 AuNPs-MoS 纳米复合材料作为信号标记,可实现对 microRNA(miRNA)的灵敏、简便测量,仅需两步即可完成。首先,将巯基修饰的 DNA 寡核苷酸探针(包括与靶 miRNA-141 互补的序列)固定在 Au 膜上,以识别靶 miRNA-141 的片段序列。然后,使用辅助的 DNA 连接的 AuNPs-MoS 纳米复合材料与 miRNA-141 的另一部分结合。利用 AuNPs-MoS 纳米复合材料增强了 SPR 生物传感器的性能,因此这种新的传感测定法对 miRNA 具有高灵敏度,检测限低至 0.5 fM。此外,该方法具有高度特异性,能够区分 miRNA-200 家族成员之间的差异。特别是,该测定法还可用于从癌细胞中检测人 miRNA,其结果与使用 qRT-PCR 获得的结果非常吻合。更重要的是,该方法可用于测定 10%人血清中的 miRNA。该方法可能为复杂样本中的 miRNA 定量方法提供巨大潜力,并在生物医学研究和临床早期诊断中发挥重要作用。