转染
核酸
小分子
纳米技术
模块化设计
基因传递
细胞质
细胞生物学
输送系统
化学
计算生物学
DNA
转导(生物物理学)
生物物理学
药物输送
内吞作用
生物
封装(网络)
信使核糖核酸
细胞
纳米颗粒
细胞培养
适体
HEK 293细胞
纳米生物技术
核糖核酸
膜
脂质体
DNA纳米技术
信号转导
靶向给药
纳米医学
基因表达
靶蛋白
细胞膜
抄写(语言学)
材料科学
膜蛋白
遗传增强
作者
Duong Luong,Nick Martel,James Rae,Harriet P. Lo,Ye‐Wheen Lim,Yeping Wu,Kerrie‐Ann McMahon,Haolan Sun,Nicholas L. Fletcher,Kristofer J. Thurecht,Angus P. R. Johnston,Nicholas Ariotti,Thomas E. Hall,Robert G. Parton
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-12-12
卷期号:19 (50): 42079-42096
标识
DOI:10.1021/acsnano.5c11452
摘要
Targeted nanoparticles have the potential to revolutionize therapeutics for medical applications. Here, we demonstrate the utility of a flexible precision nanovesicle delivery system for functional delivery of DNA, RNA, proteins, and drugs into target cells. Nanovesicles generated by the membrane sculpting protein caveolin, termed caveospheres, can be loaded with RNA, DNA, proteins, or drugs postsynthesis or incorporate genetically encoded cargo proteins during production without the need for protein purification. Functionalized, fluorescently labeled caveospheres form a modular system that shows high stability in biological fluids and specific uptake by target-positive cells and can deliver proteins, drugs, DNA, and mRNA directly to the cytoplasm and nuclei of only the target cells. The negligible level of off-target transduction and uniform levels of targeted expression demonstrate advantages of the system over lipid-mediated gene delivery. Caveospheres can also be engineered to mimic viral particles by displaying the SARS-CoV-2-RBD protein, enabling the targeted delivery to human bronchial epithelial cells. We demonstrate their application as a targeted transfection system for cells in culture and critically, their efficacy in precision tumor killing in vivo.
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