沸石咪唑盐骨架
核酸
咪唑酯
绿色荧光蛋白
转染
细胞内
纳米技术
DNA
基因表达
基因
基因传递
封装(网络)
材料科学
质粒
化学
荧光
生物物理学
纳米-
蛋白质表达
细胞
药物输送
纳米生物技术
细胞包封
细胞生物学
生物化学
HEK 293细胞
输送系统
纳米尺度
作者
Arpita Poddar,José Javier Conesa,Kang Liang,Sudip Dhakal,Philipp Reineck,Gary Bryant,Eva Pereiro,Raffaele Riccò,Heinz Amenitsch,Christian J. Doonan,Xavier Mulet,Cara M. Doherty,Paolo Falcaro,Ravi Shukla
出处
期刊:Small
[Wiley]
日期:2019-07-01
卷期号:15 (36): e1902268-e1902268
被引量:148
标识
DOI:10.1002/smll.201902268
摘要
Abstract Recent work in biomolecule‐metal–organic framework (MOF) composites has proven to be an effective strategy for the protection of proteins. However, for other biomacromolecules such as nucleic acids, the encapsulation into nano MOFs and the related characterizations are in their infancy. Herein, encapsulation of a complete gene‐set in zeolitic imidazolate framework‐8 (ZIF‐8) MOFs and cellular expression of the gene delivered by the nano MOF composites are reported. Using a green fluorescent protein (GFP) plasmid (plGFP) as a proof‐of‐concept genetic macromolecule, successful transfection of mammalian cancer cells with plGFP for up to 4 days is shown. Cell transfection assays and soft X‐ray cryo‐tomography (cryo‐SXT) demonstrate the feasibility of DNA@MOF biocomposites as intracellular gene delivery vehicles. Expression occurs over relatively prolonged time points where the cargo nucleic acid is released gradually in order to maintain sustained expression.
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