Canqiong Hu, Shuang Liu, Guoxia Huang, Fan Yang, Lexun Li, Cao Zhang, Shuxuan Shao, Xiaodan Deng, Qiaoling Liu
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引用次数: 0
Abstract
Dynamic DNA nanotechnology is appealing for membrane surface engineering due to their versatility and programmability. To modulate the dynamic interactions between the DNA functional units immobilized on membrane surface, membrane-anchored DNA functional units often come into close proximity each other due to DNA base pairing, which also leads to the close contact of the hydrophobic anchors in membrane. However, whether the close contact of hydrophobic anchors induces the dissociation of amphiphilic DNA structures from membrane surface is not concerned. Herein, we utilized cholesterol-labelled single-stranded DNA (ssDNA) as a simplified amphiphilic DNA structure to investigate the stability of membrane anchored DNA strands upon the closely contact of cholesterol anchors. The close contact of cholesterol-labelled ssDNA molecules driven by toehold mediated strand displacement reaction leads to approximately 41 % membrane anchored ssDNA dissociation from membrane surface, indicating the proximal cholesterol anchors in membrane could reduce the anchoring stability of cholesterol-modified DNA strands. This work enhances our understanding of the interactions between amphiphilic DNA and membranes, and provides valuable insights for the design of future DNA constructs intended for applications involving dynamic DNA reactions on membrane surface.
动态 DNA 纳米技术因其多功能性和可编程性而对膜表面工程具有吸引力。为了调节固定在膜表面的 DNA 功能单元之间的动态相互作用,膜锚定 DNA 功能单元往往会因 DNA 碱基配对而相互靠近,这也会导致膜中疏水锚的紧密接触。然而,疏水锚的密切接触是否会导致两亲性 DNA 结构从膜表面解离却没有得到关注。在此,我们利用胆固醇标记的单链DNA(ssDNA)作为简化的两亲性DNA结构,研究了膜锚定DNA链在胆固醇锚紧密接触时的稳定性。胆固醇标记的ssDNA分子在趾持物介导的链置换反应的驱动下紧密接触,导致约41%的膜锚定ssDNA从膜表面解离,这表明膜的近端胆固醇锚会降低胆固醇修饰的DNA链的锚定稳定性。这项研究加深了我们对两亲性 DNA 与膜之间相互作用的理解,并为设计未来用于在膜表面进行动态 DNA 反应的 DNA 构建物提供了宝贵的见解。
期刊介绍:
ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).