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A practical approach for the detection of DNA nanostructures in single live human cells by fluorescence microscopy

机译:通过荧光显微镜检测单个活人细胞中DNA纳米结构的实用方法

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In the last decade, in vivo studies have revealed that even subtle differences in size, concentration of components, cell cycle stage, make the cells in a population respond differently to the same stimulus. In order to characterize such complexity of behavior and shed more light on the functioning and communication amongst cells, researchers are developing strategies to study single live cells in a population. In this paper, we describe the methods to design and prepare DNA-based fluorescent tetrahedral nanostructures, to deliver them to live cells and characterize such cells with epifluorescence microscopy. We report that HeLa cells internalize these nanostructures spontaneously with a higher efficiency with respect to single-stranded or double-stranded oligonucleotides. Our findings suggest that DNA tetrahedra could serve as a platform for the realization of a series of multifunctional intracellular biosensors for the analysis of single live cells.
机译:在过去的十年中,体内研究表明,大小,成分浓度,细胞周期阶段的细微差异也使群体中的细胞对相同的刺激产生不同的反应。为了表征这种行为的复杂性并更加了解细胞之间的功能和交流,研究人员正在开发策略来研究种群中的单个活细胞。在本文中,我们描述了设计和制备基于DNA的荧光四面体纳米结构,将其递送至活细胞并通过落射荧光显微镜表征这些细胞的方法。我们报告说,HeLa细胞自发地以相对于单链或双链寡核苷酸的较高效率内在化这些纳米结构。我们的发现表明,DNA四面体可以作为实现用于分析单个活细胞的一系列多功能细胞内生物传感器的平台。

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