Koep Abigail, Masud Nabila, Van't Hul Jaylie, Stanley Carson, Nilsen-Hamilton Marit, Sarkar Anwesha, Schneider Ian C
Department of Chemical and Biological Engineering, Iowa State University, Ames, Iowa 50011, United States.
Department of Electrical and Computer Engineering, Iowa State University, Ames, Iowa 50011, United States.
ACS Appl Bio Mater. 2025 Aug 18;8(8):7188-7200. doi: 10.1021/acsabm.5c00907. Epub 2025 Aug 5.
DNA origami, a method of folding DNA into precise nanostructures, has emerged as a powerful tool for the design of complex nanoscale shapes. It has great potential as a technology to encapsulate and release cargos spanning small molecules through large proteins, while remaining stable in a variety of processing conditions and environments. While DNA origami has been utilized for drug delivery applications, the vast majority of these structures have been flexible, flat 2D or solid 3D nanostructures. There is a crucial need for a hollow and completely enclosed design capable of holding and eventually releasing a variety of cargos. In this paper, we present the design and assembly of a hollow DNA origami box with two lids. We characterize the isothermal conditions for structural assembly within minutes. We demonstrate that passive loading of small molecules is charge dependent. We also outline an approach to design staple extensions pointing into the cavity or outside of the hollow DNA origami, allowing for the active loading of protein or the potential for decoration with passivating or targeting molecules.
DNA折纸术是一种将DNA折叠成精确纳米结构的方法,已成为设计复杂纳米级形状的强大工具。作为一种技术,它具有巨大的潜力,可用于封装和释放从小分子到大型蛋白质的各种货物,同时在各种加工条件和环境中保持稳定。虽然DNA折纸术已被用于药物递送应用,但这些结构绝大多数都是灵活的、扁平的二维或实心的三维纳米结构。迫切需要一种能够容纳并最终释放各种货物的中空且完全封闭的设计。在本文中,我们展示了一种带有两个盖子的中空DNA折纸盒的设计与组装。我们表征了在几分钟内进行结构组装的等温条件。我们证明小分子的被动装载是电荷依赖性的。我们还概述了一种设计钉状延伸的方法,使其指向中空DNA折纸的腔内或外部,从而实现蛋白质的主动装载或用钝化或靶向分子进行修饰的可能性。