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通过定量聚合酶链反应(qPCR)对DNA纳米结构的细胞摄取进行定量分析。

Quantification of cellular uptake of DNA nanostructures by qPCR.

作者信息

Okholm Anders Hauge, Nielsen Jesper Sejrup, Vinther Mathias, Sørensen Rasmus Schøler, Schaffert David, Kjems Jørgen

机构信息

Interdisciplinary Nanoscience Center, Aarhus University, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark; Department of Molecular Biology, Aarhus University, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark; Centre for DNA Nanotechnology, Aarhus University, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark.

Interdisciplinary Nanoscience Center, Aarhus University, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark; Department of Molecular Biology, Aarhus University, Gustav Wieds Vej 14, DK-8000 Aarhus C, Denmark.

出版信息

Methods. 2014 May 15;67(2):193-7. doi: 10.1016/j.ymeth.2014.01.013. Epub 2014 Jan 25.

Abstract

DNA nanostructures facilitating drug delivery are likely soon to be realized. In the past few decades programmed self-assembly of DNA building blocks have successfully been employed to construct sophisticated nanoscale objects. By conjugating functionalities to DNA, other molecules such as peptides, proteins and polymers can be precisely positioned on DNA nanostructures. This exceptional ability to produce modular nanoscale devices with tunable and controlled behavior has initiated an interest in employing DNA nanostructures for drug delivery. However, to obtain this the relationship between cellular interactions and structural and functional features of the DNA delivery device must be thoroughly investigated. Here, we present a rapid and robust method for the precise quantification of the component materials of DNA origami structures capable of entering cells in vitro. The quantification is performed by quantitative polymerase chain reaction, allowing a linear dynamic range of detection of five orders of magnitude. We demonstrate the use of this method for high-throughput screening, which could prove efficient to identify key features of DNA nanostructures enabling cell penetration. The method described here is suitable for quantification of in vitro uptake studies but should easily be extended to quantify DNA nanostructures in blood or tissue samples.

摘要

促进药物递送的DNA纳米结构可能很快就会实现。在过去几十年里,DNA构建模块的程序化自组装已成功用于构建复杂的纳米级物体。通过将功能基团与DNA结合,其他分子如肽、蛋白质和聚合物可以精确地定位在DNA纳米结构上。这种制造具有可调谐和可控行为的模块化纳米级装置的特殊能力引发了人们对利用DNA纳米结构进行药物递送的兴趣。然而,要实现这一点,必须深入研究细胞相互作用与DNA递送装置的结构和功能特征之间的关系。在此,我们提出了一种快速且可靠的方法,用于精确量化能够在体外进入细胞的DNA折纸结构的组成材料。该量化通过定量聚合酶链反应进行,检测的线性动态范围可达五个数量级。我们展示了该方法用于高通量筛选的用途,这可能被证明对于识别使细胞穿透成为可能的DNA纳米结构的关键特征是有效的。这里描述的方法适用于体外摄取研究的量化,但应该很容易扩展到对血液或组织样本中的DNA纳米结构进行量化。

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