小干扰RNA
核酸
DNA
基因沉默
内吞作用
生物物理学
纳米技术
细胞内
细胞生物学
RNA干扰
核糖核酸
DNA纳米技术
小分子
化学
生物
细胞
计算生物学
材料科学
生物化学
基因
作者
Jie Li,Xiuhai Mao,Tiantian Zhao,Weina Fang,Yangyang Jin,Mengmeng Liu,Chunhai Fan,Yang Tian
标识
DOI:10.1002/anie.202416988
摘要
Spherical nucleic acids (SNAs) hold substantial therapeutic potential for the delivery of small interfering RNAs (siRNAs). Nevertheless, their potential remains largely untapped due to the challenges of cytosolic delivery. Inspired by the dynamic, spiky architecture of coronavirus, an interface engineering approach based on a tetrahedral DNA framework (tDF) is demonstrated for the development of coronavirus‐mimicking SNAs. By exploiting their robustness and precise construction, tDFs are evenly arranged on the surface of core nanoparticles (NPs) with flexible conformations, generating a dynamic, spiky architecture. This spiky architecture in tetrahedral DNA framework‐based SNAs (tDF‐SNAs) substantially improve siRNAs duplex efficiency from 20% to 95%. Meanwhile, tDF‐SNAs changed the endocytosis pathway to clathrin‐independent cellular engulfment pathway and enhanced the cellular uptake efficiency. Due to these advances, the delivery efficiency of siRNA molecules by tDF‐SNAs is 1‐2 orders of magnitude higher than that of SNAs, resulting in a 2‐fold increase in gene silencing efficacy. These results show promise in the development of bioinspired siRNAs delivery systems for intracellular applications.
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