State Key Laboratory of Chemo/Bio-Sensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University , Changsha 410082, P. R. China.
Anal Chem. 2017 Nov 21;89(22):12351-12359. doi: 10.1021/acs.analchem.7b03369. Epub 2017 Nov 8.
MicroRNAs (miRNAs) play important roles in cell differentiation, proliferation, and apoptosis and have been recognized as valuable biomarkers for clinical disease diagnosis. Here, we adopt for the first time zeolitic imidazolate framework-8 (ZIF-8) as a nanocarrier to efficiently deliver a nucleic acid probe to living cells and develop a novel ratiometric fluorescence strategy based on DNAzyme for miRNA-21 imaging. A Cy5-labeled 8-17 DNAzyme strand and a Cy3-labeled substrate strand containing a segment complementary to the target miRNA-21 first form a duplex probe, and fluorescence resonance energy transfer (FRET) takes place. After adsorption on the ZIF-8 surface and cellular uptake, the probe/ZIF-8 nanocomplex degrades in acidic endosome and releases duplex probes and Zn, and the latter can act as an effective cofactor for 8-17 DNAzyme. The intracellular miRNA-21 hybridizes with the complementary segment of the substrate strand and results in dissociation from the DNAzyme-substrate duplex probe after DNAzyme cleaves the substrate into two fragments, accompanied by the change in the FRET signal. The proposed method has been applied to image miRNA-21 expression levels in MCF-7, HeLa, and L02 cells with high contrast and reliability. The fluctuation of miRNA-21 expression level induced by miRNA-21 mimic or inhibitor can also be monitored through the obvious imaging color change. Taken together, the proposed method provides a powerful tool for cancer diagnosis and miRNA-associated biological study.
微小 RNA(miRNAs)在细胞分化、增殖和凋亡中发挥重要作用,已被认为是临床疾病诊断有价值的生物标志物。在这里,我们首次采用沸石咪唑酯骨架-8(ZIF-8)作为纳米载体,将核酸探针高效递送至活细胞,并基于 DNA 酶开发了一种新型的比率荧光策略,用于 miRNA-21 的成像。Cy5 标记的 8-17 DNA 酶链和含有与靶 miRNA-21 部分互补的 Cy3 标记的底物链首先形成双链探针,并发生荧光共振能量转移(FRET)。在吸附在 ZIF-8 表面和细胞摄取后,探针/ZIF-8 纳米复合物在酸性内涵体中降解,并释放双链探针和 Zn,后者可以作为 8-17 DNA 酶的有效辅因子。细胞内的 miRNA-21 与底物链的互补片段杂交,在 DNA 酶将底物切割成两个片段后,从 DNA 酶-底物双链探针中解离出来,伴随着 FRET 信号的变化。该方法已成功应用于 MCF-7、HeLa 和 L02 细胞中 miRNA-21 表达水平的高对比度和高可靠性成像。通过明显的成像颜色变化,还可以监测 miRNA-21 模拟物或抑制剂诱导的 miRNA-21 表达水平的波动。总之,该方法为癌症诊断和 miRNA 相关的生物学研究提供了一种强大的工具。