Ian Potter NanoBiosensing Facility, NanoBiotechnology Research Laboratory (NBRL), School of Science, RMIT University, Melbourne, Victoria, 3001, Australia.
CSIRO Manufacturing, Clayton, Victoria, 3168, Australia.
Small. 2019 Sep;15(36):e1902268. doi: 10.1002/smll.201902268. Epub 2019 Jul 1.
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.
最近在生物分子-金属有机骨架(MOF)复合材料方面的研究证明,这是保护蛋白质的一种有效策略。然而,对于其他生物大分子,如核酸,将其封装到纳米 MOF 中以及相关的特性研究还处于起步阶段。在此,我们报告了完整的基因集在沸石咪唑酯骨架-8(ZIF-8)MOF 中的封装,以及由纳米 MOF 复合材料递送的基因在细胞中的表达。使用绿色荧光蛋白(GFP)质粒(plGFP)作为概念验证遗传大分子,证明了 plGFP 可以成功转染哺乳动物癌细胞长达 4 天。细胞转染实验和软 X 射线冷冻断层扫描(cryo-SXT)表明 DNA@MOF 生物复合材料作为细胞内基因传递载体的可行性。这种表达可以持续较长的时间点,其中货物核酸逐渐释放,以维持持续表达。