Key Laboratory of Luminescence Analysis and Molecular Sensing (Southwest University), Ministry of Education, College of Pharmaceutical Sciences, Southwest University, Chongqing 400715, P. R. China.
State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, 2 Sipailou Road, Nanjing, Jiangsu 210096, P. R. China.
ACS Appl Bio Mater. 2021 Apr 19;4(4):3469-3475. doi: 10.1021/acsabm.1c00029. Epub 2021 Mar 11.
MicroRNAs, as one kind of significant biomarkers, play indispensable roles in the diagnosis and treatment of cancers. Yet, owing to low expression and high sequence homology, high sensitivity and specificity for microRNA detection are greatly challenging. Herein, a sensitive sensing platform with high specificity was developed for microRNA-27a (miRNA-27a) based on the miRNA-27a-triggered chemical etching of gold nanorods to a smaller size, which was accompanied by a significant blue shift and a large decrease of intensity in the localized surface plasmon resonance (LSPR) scattering and remarkable color variability from red to green. When combined with strand displacement reactions as well as liposome signal amplification and transduction, the proposed bioassay presented high selectivity toward miRNA-27a in a dynamic range from 100 fM to 3 pM and a low limit of detection of 16.5 fM (3σ/) by dark-field microscopy. Additionally, the remarkable discrimination of single nucleotide difference suggested superior selectivity and was able to detect miRNA-27a extracted from breast cancer cells. The strategy put forward is universal, presenting amusing application prospects in the early diagnosis of various cancers by adapting the corresponding nucleotide sequences.
微小 RNA 作为一种重要的生物标志物,在癌症的诊断和治疗中发挥着不可或缺的作用。然而,由于其表达量低且序列同源性高,因此对微小 RNA 的检测需要高度的灵敏度和特异性,这极具挑战性。在此,我们基于微小 RNA-27a(miRNA-27a)触发的金纳米棒的化学刻蚀,开发了一种具有高特异性的灵敏传感平台,该刻蚀会导致金纳米棒的尺寸变小,同时伴随局域表面等离子体共振(LSPR)散射的显著蓝移和强度的大幅降低,以及颜色从红色到绿色的显著变化。当与链置换反应以及脂质体信号放大和转导相结合时,该生物分析方法在 100 fM 至 3 pM 的动态范围内对 miRNA-27a 表现出高选择性,检测限低至 16.5 fM(3σ/),通过暗场显微镜进行检测。此外,单核苷酸差异的显著区分表明了其具有优越的选择性,并且能够检测从乳腺癌细胞中提取的 miRNA-27a。该策略具有通用性,通过适应相应的核苷酸序列,为通过早期诊断各种癌症提供了有趣的应用前景。