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胆固醇锚定促进 DNA 纳米结构的高效结合和细胞内摄取。

Cholesterol Anchors Enable Efficient Binding and Intracellular Uptake of DNA Nanostructures.

机构信息

Department of Chemistry, Institute of Structural and Molecular Biology , University College London , London WC1H 0AJ , United Kingdom.

National Physical Laboratory , Hampton Road , Teddington TW11 0LW , United Kingdom.

出版信息

Bioconjug Chem. 2019 Jul 17;30(7):1836-1844. doi: 10.1021/acs.bioconjchem.9b00036. Epub 2019 Mar 1.

Abstract

DNA nanostructures constitute a rapidly advancing tool-set for exploring cell-membrane functions and intracellular sensing or advancing delivery of biomolecular cargo  into cells. Chemical conjugation with lipid anchors can mediate binding of DNA nanostructures to synthetic lipid bilayers, yet how such structures interact with biological membranes and internalize cells has not been shown. Here, an archetypal 6-duplex nanobundle is used to investigate how lipid conjugation influences DNA cell binding and internalization kinetics. Cellular interactions of DNA nanobundles modified with one and three cholesterol anchors were assessed using flow cytometry and confocal microscopy. Nuclease digestion was used to distinguish surface-bound DNA, which is nuclease accessible, from internalized DNA. Three cholesterol anchors were found to enhance cellular association by up to 10-fold when compared with unmodified DNA. The bundles were endocytosed efficiently within 24 h. The results can help design controlled DNA binding and trafficking into cells.

摘要

DNA 纳米结构是一种快速发展的工具集,可用于探索细胞膜功能和细胞内感应,或促进生物分子货物递送至细胞内。通过化学偶联与脂质锚定可以介导 DNA 纳米结构与合成脂质双层的结合,但这些结构如何与生物膜相互作用并内化细胞尚未得到证明。在这里,使用典型的 6 个双链纳米束来研究脂质偶联如何影响 DNA 细胞结合和内化动力学。使用流式细胞术和共聚焦显微镜评估了用一个和三个胆固醇锚修饰的 DNA 纳米束的细胞相互作用。使用核酸酶消化来区分表面结合的 DNA,其可被核酸酶接近,与内化的 DNA 区分开来。与未修饰的 DNA 相比,发现三个胆固醇锚可将细胞相关性提高多达 10 倍。这些束在 24 小时内被有效内吞。这些结果有助于设计受控的 DNA 结合和细胞内运输。

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