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基于荧光共振能量转移(FRET)效应的荧光强度编码 DNA 框架可实现活细胞中多重 miRNA 的成像。

Fluorescence intensity coded DNA frameworks based on the FRET effect enable multiplexed miRNA imaging in living cells.

机构信息

Key Laboratory of Functional Materials for Informatics, Shanghai Institute of Microsystems and Information Technology, Chinese Academy of Science, Shanghai 200050, China.

University of Chinese Academy of Science, Beijing 100049, China.

出版信息

Anal Methods. 2023 Jun 29;15(25):3051-3056. doi: 10.1039/d3ay00578j.

Abstract

miRNA analysis has played an important role in precise diagnosis, treatment and prognosis of cancer, especially multiplexed miRNA imaging. In this work, a novel fluorescence emission intensity (FEI) encoding strategy was developed based on a tetrahedron DNA framework (TDF) carrier and the FRET effect between Cy3 and Cy5. Six FEI-encoded TDF (FEI-TDF) samples were constructed by tuning the labeling number of Cy3 and Cy5 at the vertexes of the TDF. For fluorescence characterization , distinct FEIs in the spectra and different colors under ultraviolet (UV) irradiation of FEI-TDF samples were observed. By dividing the ranges of FEIs of samples, the stability of FEIs was highly improved. Based on the ranges of FEIs in each sample, five codes with good discrimination were finally developed. Before the application of intracellular imaging, the excellent biocompatibility of the TDF carrier was proved by CCK-8 assay. The barcode probes based on samples 12, 21 and 11 were designed as example models to realize multiplexed imaging of miRNA-16, miRNA-21 and miRNA-10b in MCF-7 cells with obviously different fluorescence merged colors. FEI-TDFs provide a new research perspective for the development of fluorescence multiplexing strategies in the future.

摘要

miRNA 分析在癌症的精确诊断、治疗和预后中发挥了重要作用,尤其是多重 miRNA 成像。在这项工作中,基于四面体 DNA 框架(TDF)载体和 Cy3 和 Cy5 之间的 FRET 效应,开发了一种新的荧光发射强度(FEI)编码策略。通过调整 TDF 顶点处 Cy3 和 Cy5 的标记数量,构建了六个 FEI 编码的 TDF(FEI-TDF)样品。为了进行荧光表征,观察到 FEI-TDF 样品在光谱中具有明显不同的 FEI 和在紫外线(UV)照射下的不同颜色。通过划分样品 FEI 的范围,FEI 的稳定性得到了极大的提高。基于每个样品的 FEI 范围,最终开发了五个具有良好区分度的代码。在进行细胞内成像之前,通过 CCK-8 测定证明了 TDF 载体的优异生物相容性。基于样品 12、21 和 11 设计的条码探针作为示例模型,实现了 MCF-7 细胞中 miRNA-16、miRNA-21 和 miRNA-10b 的多重成像,具有明显不同的荧光融合颜色。FEI-TDF 为未来荧光多重化策略的发展提供了新的研究视角。

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