Department of Chemical Sciences and Technologies, University of Rome, Tor Vergata, Via della Ricerca Scientifica, 00133 Rome, Italy.
Biomedical Engineering Department, Institute for Complex Molecular Systems, Technische Universiteit Eindhoven, Het Kranenveld 14, 5612 AZ Eindhoven, The Netherlands.
J Am Chem Soc. 2024 May 8;146(18):12664-12671. doi: 10.1021/jacs.4c02094. Epub 2024 Apr 8.
Here, we report DNA-based synthetic nanostructures decorated with enzymes (hereafter referred to as DNA-enzyme swimmers) that self-propel by converting the enzymatic substrate to the product in solution. The DNA-enzyme swimmers are obtained from tubular DNA structures that self-assemble spontaneously by the hybridization of DNA tiles. We functionalize these DNA structures with two different enzymes, urease and catalase, and show that they exhibit concentration-dependent movement and enhanced diffusion upon addition of the enzymatic substrate (i.e., urea and HO). To demonstrate the programmability of such DNA-based swimmers, we also engineer DNA strands that displace the enzyme from the DNA scaffold, thus acting as molecular "brakes" on the DNA swimmers. These results serve as a first proof of principle for the development of synthetic DNA-based enzyme-powered swimmers that can self-propel in fluids.
在这里,我们报告了一种基于 DNA 的合成纳米结构,其表面装饰有酶(此后称为 DNA-酶游动体),这些游动体能通过将酶的底物转化为溶液中的产物而自行推进。这些 DNA-酶游动体是从管状 DNA 结构获得的,这些管状 DNA 结构通过 DNA 瓦片的杂交自发自组装而成。我们用两种不同的酶(脲酶和过氧化氢酶)对这些 DNA 结构进行功能化,并表明它们在添加酶底物(即尿素和 HO)时表现出浓度依赖性运动和增强的扩散。为了证明这种基于 DNA 的游动体的可编程性,我们还设计了 DNA 链,使酶从 DNA 支架上置换出来,从而对 DNA 游动体起到分子“刹车”的作用。这些结果为开发可在液体中自行推进的合成 DNA 酶动力游动体提供了初步的原理证明。