Wang Dong, Chen Chunfa, Liu Qian, Zhao Qianwen, Wu Di, Yuan Yue, Huang Chaowang, Sun Xiaorong, Huang Chunji, Leong David Tai, Wang Guansong, Qian Hang
Institute of Respiratory Diseases, Xinqiao Hospital, Third Military Medical University, 183 Xinqiao Street, Chongqing, 400037, China.
Department of Respiratory Medicine, Jinling Hospital, Nanjing, Jiangsu, 210002, China.
Bioact Mater. 2021 Feb 27;6(9):2946-2955. doi: 10.1016/j.bioactmat.2021.02.012. eCollection 2021 Sep.
Complexing self-assembled DNA nanostructures with various functional guest species is the key to unlocking new and exciting biomedical applications. Cationic guest species not only induce magnesium-free DNA to self-assemble into defined structures but also endow the final complex nanomaterials with new properties. Herein, we propose a novel strategy that employs naturally occurring cationic amino acids to induce DNA self-assembly into defined nanostructures. Natural l-arginine and l-lysine can readily induce the assembly of tile-based DNA nanotubes and DNA origami sheets in a magnesium-free manner. The self-assembly processes are demonstrated to be pH- and concentration-dependent and are achieved at constant temperatures. Moreover, the assembled DNA/amino acid complex nanomaterials are stable at a physiological temperature of 37 °C. Substituting l-arginine with its D form enhances its serum stability. Further preliminary examination of this complex nanomaterial platform for biomedical applications indicates that DNA/amino acids exhibit distinct cellular uptake behaviors compared with their magnesium-assembled counterparts. The nanomaterial mainly clusters around the cell membrane and might be utilized to manipulate molecular events on the membrane. Our study suggests that the properties of DNA nanostructures can be tuned by complexing them with customized guest molecules for a designed application. The strategy proposed herein might be promising to advance the biomedical applications of DNA nanostructures.
将各种功能性客体物种与自组装的DNA纳米结构复合是开启新的、令人兴奋的生物医学应用的关键。阳离子客体物种不仅能诱导无镁的DNA自组装成特定结构,还能赋予最终的复合纳米材料新的性质。在此,我们提出了一种新策略,即利用天然存在的阳离子氨基酸诱导DNA自组装成特定的纳米结构。天然的L-精氨酸和L-赖氨酸能够以无镁的方式轻易诱导基于瓦片的DNA纳米管和DNA折纸片的组装。自组装过程被证明是pH和浓度依赖性的,并且在恒定温度下实现。此外,组装好的DNA/氨基酸复合纳米材料在37℃的生理温度下是稳定的。用其D型取代L-精氨酸可提高其血清稳定性。对这种复合纳米材料平台进行生物医学应用的进一步初步研究表明,与镁组装的对应物相比,DNA/氨基酸表现出不同的细胞摄取行为。这种纳米材料主要聚集在细胞膜周围,可能被用于操控膜上的分子事件。我们的研究表明,通过将DNA纳米结构与定制的客体分子复合以用于设计的应用,可以调节其性质。本文提出的策略可能有望推动DNA纳米结构的生物医学应用。