核酸
DNA
胞浆
化学
生物化学
细胞生物学
纳米技术
生物物理学
计算生物学
生物
酶
材料科学
作者
Di Gao,Ziqi Xu,Xiangli Li,Yuhan Zhao,Qianhao Min,Zixuan Chen,Qin Xu,Ye Tian,Junpeng Xu,Junjie Zhu
标识
DOI:10.1002/ange.202505290
摘要
Delivering biomacromolecules to the cytosol remains a formidable challenge, as these molecules are predominantly sequestered within endosomes after endocytosis. The limited efficacy of current delivery systems in promoting reliable endosomal escape underscores the need for innovative strategies. Here, we report a DNA origami nanotubule to construct transmembrane delivery nanodevices with size‐selective gating and ATP‐responsive channel activation. By integrating unilamellar vesicles as large storage compartments, these nanodevices can encapsulate a wide range of macromolecules, including small interfering RNA, messenger RNA, plasmid DNA, and CRISPR‐Cas9 ribonucleoprotein complexes. By bypassing traditional endocytic pathways, the nanotubules enable the delivery of substantial payload quantities directly across the plasma membrane. This approach provides a promising platform for delivering macromolecular therapeutics into the cytosol, advancing gene therapy strategies, and broadening their biomedical applications.
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