共价键
纳米笼
DNA折纸
DNA
四面体
材料科学
生物物理学
内化
纳米团簇
纳米技术
纳米结构
结晶学
化学
受体
生物化学
生物
有机化学
催化作用
作者
Sofia Raniolo,Stefano Croce,Rasmus P. Thomsen,Anders Hauge Okholm,Valeria Unida,Federico Iacovelli,Antonio Manetto,Jørgen Kjems,Alessandro Desideri,Silvia Biocca
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2019-01-01
卷期号:11 (22): 10808-10818
被引量:43
摘要
DNA nanostructures with different sizes and shapes, assembled through either covalent or non-covalent bonds, namely tetrahedral and octahedral nanocages, rod-shaped chainmails, square box and rectangular DNA origami structures, were compared for their stability in serum, cell surface binding, internalization efficiency, and intracellular degradation rate. For cell internalization a specific cell system, highly expressing the scavenger receptor LOX-1 was used. The results indicate that LOX-1 binds and internalizes a broad family of DNA structures of different sizes that, however, have a different fate and lifetime inside the cells. Covalently linked tetrahedra, octahedra or chainmails are intact inside cells for up to 18 hours whilst the same DNA nanostructures without covalent bonds along with square box and rectangular origami are rapidly degraded. These data suggest that non-covalently linked structures may be useful for fast drug release whilst the covalently-linked structures could be appropriate vehicles for slow release of molecules.
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