Phosphorothioated DNA Engineered Liposomes as a General Platform for Stimuli-Responsive Cell-Specific Intracellular Delivery and Genome Editing

被引:28
作者
Yan, An [1 ]
Chen, Xiaoqing [1 ]
He, Jie [1 ]
Ge, Yifan [2 ]
Liu, Qing [3 ]
Men, Dong [4 ]
Xu, Ke [5 ]
Li, Di [1 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai 200241, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, Interdisciplinary Res Ctr Biol & Chem, Shanghai 201210, Peoples R China
[3] Shanghai Jiao Tong Univ, Rui Jin Hosp, Sch Med, Shanghai 200025, Peoples R China
[4] Guangzhou Lab, Guangzhou 510005, Peoples R China
[5] Wuhan Univ, Coll Life Sci, State Key Lab Virol, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
Cell-Specific; Genome Editing; Hemagglutinin-Mimicking; Phosphorothioated DNA; Protein Delivery; MEMBRANE-FUSION; NANOCARRIERS; STRATEGIES; DEPENDENCE; THERAPY;
D O I
10.1002/anie.202303973
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Intracellular protein delivery is highly desirable for protein drug-based cell therapy. Established technologies suffer from poor cell-specific cytosolic protein delivery, which hampers the targeting therapy of specific cell populations. A fusogenic liposome system enables cytosolic delivery, but its ability of cell-specific and controllable delivery is quite limited. Inspired by the kinetics of viral fusion, we designed a phosphorothioated DNA coatings-modified fusogenic liposome to mimic the function of viral hemagglutinin. The macromolecular fusion machine docks cargo-loaded liposomes at the membrane of target cells, triggers membrane fusion upon pH or UV light stimuli, and facilitates cytosolic protein delivery. Our results showed efficient cell-targeted delivery of proteins of various sizes and charges, indicating the phosphorothioated DNA plug-in unit on liposomes could be a general strategy for spatial-temporally controllable protein delivery both in vitro and in vivo.
引用
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页数:10
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