Department of Chemistry, University of Rome Tor Vergata, Via della Ricerca Scientifica, Rome, 00133, Italy.
Adv Mater. 2023 May;35(18):e2211274. doi: 10.1002/adma.202211274. Epub 2023 Mar 19.
An approach to achieving dynamic and reversible decoration of DNA-based scaffolds is demonstrated here. To do this, rationally engineered DNA tiles containing enzyme-responsive strands covalently conjugated to different molecular labels are employed. These strands are designed to be recognized and degraded by specific enzymes (i.e., Ribonuclease H, RNase H, or Uracil DNA Glycosylase, UDG) inducing their spontaneous de-hybridization from the assembled tile and replacement by a new strand conjugated to a different label. Multiple enzyme-responsive strands that specifically respond to different enzymes allow for dynamic, orthogonal, and reversible decoration of the DNA structures. As a proof-of-principle of the strategy, the possibility to orthogonally control the distribution of different labels (i.e., fluorophores and small molecules) on the same scaffold without crosstalk is demonstrated. By doing so, DNA scaffolds that display different antibody recognition patterns are obtained. The approach offers the possibility to control the decoration of higher-order supramolecular assemblies (including origami) with several functional moieties to achieve functional biomaterials with improved adaptability, precision, and sensing capabilities.
本文展示了一种实现基于 DNA 的支架动态可逆修饰的方法。为此,使用了经过合理设计的含有酶响应链的 DNA 瓦片,这些酶响应链共价连接到不同的分子标签上。这些链被设计为被特定的酶(即核糖核酸酶 H、RNase H 或尿嘧啶 DNA 糖基化酶 UDG)识别和降解,从而导致它们从组装的瓦片中自发解链,并被连接到不同标签的新链取代。多个专门针对不同酶的酶响应链允许对 DNA 结构进行动态、正交和可逆的修饰。作为该策略的原理验证,证明了在不发生串扰的情况下,在同一支架上正交控制不同标签(即荧光团和小分子)分布的可能性。通过这样做,获得了显示不同抗体识别模式的 DNA 支架。该方法为用几个功能部分控制更高级别超分子组装(包括折纸)的修饰提供了可能性,从而实现具有更好适应性、精度和传感能力的功能性生物材料。