Yu Yifan, Ji Min, Wang Yong, Yan Xuehui, Dai Lizhi, Ma Ningning, Zhou Zhaoyu, Xing Hang, Tian Ye
College of Engineering and Applied Sciences, State Key Laboratory of Analytical Chemistry for Life Science, National Laboratory of Solid State Microstructures, Jiangsu Key Laboratory of Artificial Functional Materials, Chemistry and Biomedicine Innovation Center, Collaborative Innovation Center of Advanced Microstructures, Nanjing University Nanjing 210023 China
Institute of Chemical Biology and Nanomedicine, State Key Laboratory of Chemo/Biosensing and Chemometrics, Hunan Provincial Key Laboratory of Biomacromolecular Chemical Biology, College of Chemistry and Chemical Engineering, Hunan University Changsha 410082 China.
Chem Sci. 2024 Dec 4;16(2):793-801. doi: 10.1039/d4sc07267g. eCollection 2025 Jan 2.
Structural DNA nanotechnology makes the programmable design and assembly of DNA building blocks into user-defined microstructures feasible. However, the formation and further growth of these microstructures requires slow heat treatment in precise instruments, as otherwise amorphous aggregates result. Here, we used an organic solute, urea, as the catalyst for the crystallization of DNA origami building blocks to achieve the fast synthesis of DNA origami single crystals with a cubic Wulff shape at room temperature. The ordered assemblies can be formed within 4 hours at room temperature, which further grew into cubic microcrystals with an average size of about 5 micrometers within 2 days. Furthermore, the phase diagram provides an inverse logic that allows users to proactively customize the melting temperature ( ) of crystallization according to the target temperature conditions, rather than requiring design of DNA sequences or painstakingly difficult trial-and-error attempts. On this basis, even under random fluctuating outdoor temperature conditions, DNA origami crystals can still grow and maintain high quality and high yield comparable to those of crystals synthesized in precise instruments, creating a basis for the development of adaptive self-assemblies and the industrialization of functional DNA microstructures.
结构DNA纳米技术使将DNA构建模块可编程设计和组装成用户定义的微结构成为可能。然而,这些微结构的形成和进一步生长需要在精密仪器中进行缓慢的热处理,否则会形成无定形聚集体。在这里,我们使用有机溶质尿素作为DNA折纸构建模块结晶的催化剂,以在室温下快速合成具有立方乌尔夫形状的DNA折纸单晶。有序组装体可在室温下4小时内形成,并在2天内进一步生长成平均尺寸约为5微米的立方微晶。此外,相图提供了一种反向逻辑,允许用户根据目标温度条件主动定制结晶的熔化温度( ),而无需设计DNA序列或进行极其困难的反复试验。在此基础上,即使在随机波动的室外温度条件下,DNA折纸晶体仍能生长并保持与在精密仪器中合成的晶体相当的高质量和高产量,为适应性自组装的发展和功能性DNA微结构的工业化创造了基础。