Shen Xiaotong, Ouyang Qingwen, Tan Hongwei, Ouyang Jin, Na Na
Key Laboratory of Radiopharmaceuticals, Ministry of Education, College of Chemistry, Beijing Normal University, Beijing 100875, China.
Department of Chemistry, College of Arts and Sciences, Beijing Normal University at Zhuhai, Zhuhai City, Guangdong Province, 519087, China.
Anal Chem. 2023 Apr 11;95(14):5903-5910. doi: 10.1021/acs.analchem.2c04916. Epub 2023 Mar 31.
Single-stranded DNA (ssDNA) allows flexible and directional modifications for multiple biological applications, while being greatly limited by their poor stability, increased folding errors, and complicated sequence optimizations. This greatly challenges the design and optimization of ssDNA sequences to fold stable 3D structures for diversified bioapplications. Herein, the stable pentahedral ssDNA framework nanorobots (ssDNA nanorobots) were intelligently designed, assisted by examining dynamic folding of ssDNA in self-assemblies via all-atom molecular dynamics simulations. Assisted by two functional siRNAs (S1 and S2), two ssDNA strands were successfully assembled into ssDNA nanorobots, which include five functional modules (skeleton fixation, logical dual recognition of tumor cell membrane proteins, enzyme loading, dual-miRNA detection and synergy siRNA loading) for multiple applications. By both theoretical calculations and experiments, ssDNA nanorobots were demonstrated to be stable, flexible, highly utilized with low folding errors. Thereafter, ssDNA nanorobots were successfully applied to logical dual-recognition targeting, efficient and cancer-selective internalization, visual dual-detection of miRNAs, selective siRNA delivery and synergistic gene silencing. This work has provided a computational pathway for constructing flexible and multifunctional ssDNA frameworks, enlarging biological application of nucleic acid nanostructures.
单链DNA(ssDNA)可为多种生物学应用提供灵活且定向的修饰,但其稳定性差、折叠错误增加以及序列优化复杂等问题极大地限制了它的应用。这给设计和优化ssDNA序列以折叠出稳定的三维结构用于多样化生物应用带来了巨大挑战。在此,通过全原子分子动力学模拟研究ssDNA在自组装中的动态折叠,智能设计出了稳定的五面体ssDNA框架纳米机器人(ssDNA纳米机器人)。在两种功能性小干扰RNA(S1和S2)的辅助下,两条ssDNA链成功组装成ssDNA纳米机器人,其包含五个功能模块(骨架固定、肿瘤细胞膜蛋白的逻辑双重识别、酶负载、双微小RNA检测和协同小干扰RNA负载)用于多种应用。通过理论计算和实验均证明,ssDNA纳米机器人具有稳定性、灵活性,利用率高且折叠错误低。此后,ssDNA纳米机器人成功应用于逻辑双重识别靶向、高效且癌症选择性内化、微小RNA的可视化双重检测、选择性小干扰RNA递送以及协同基因沉默。这项工作为构建灵活且多功能的ssDNA框架提供了一条计算途径,扩大了核酸纳米结构的生物学应用。