核糖核酸
核苷
表观遗传学
计算生物学
化学
纳米技术
生物
核苷酸
抄写(语言学)
生物化学
基因
材料科学
语言学
哲学
作者
Kun Dai,Gong Chen,Yang Xu,Fei Ding,Xiaodong Qi,Xinyi Tu,Yu Lu,Xiaoguo Liu,Jiang Li,Chunhai Fan,Hao Yan,Guangbao Yao
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-07-27
卷期号:23 (15): 7188-7196
被引量:6
标识
DOI:10.1021/acs.nanolett.3c02185
摘要
The integration of functional modules at the molecular level into RNA nanostructures holds great potential for expanding their applications. However, the quantitative integration of nucleoside analogue molecules into RNA nanostructures and their impact on the structure and function of RNA nanostructures remain largely unexplored. Here, we report a transcription-based approach to controllably integrate multiple nucleoside analogues into a 2000 nucleotide (nt) single-stranded RNA (ssRNA) origami nanostructure. The resulting integrated ssRNA origami preserves the morphology and biostability of the original ssRNA origami. Moreover, the integration of nucleoside analogues introduced new biomedical functions to ssRNA origamis, including innate immune recognition and regulation after the precise integration of epigenetic nucleoside analogues and synergistic effects on tumor cell killing after integration of therapeutic nucleoside analogues. This study provides a promising approach for the quantitative integration of functional nucleoside analogues into RNA nanostructures at the molecular level, thereby offering valuable insights for the development of multifunctional ssRNA origamis.
科研通智能强力驱动
Strongly Powered by AbleSci AI