生物矿化
材料科学
纳米结构
DNA
细胞外基质
生物物理学
磷酸盐
成核
无定形磷酸钙
纳米技术
钙
磷灰石
化学工程
生物化学
化学
矿物学
生物
冶金
有机化学
工程类
作者
Alexander L. Danesi,Dimitra Athanasiadou,Abdulmateen O. Aderinto,Prakash Rasie,Leo Y. T. Chou,Karina M. M. Carneiro
标识
DOI:10.1021/acsami.1c19271
摘要
The guiding principle for mineralized tissue formation is that mineral growth occurs through the interaction of Ca2+ and phosphate ions with extracellular matrix (ECM) proteins. Recently, nanoengineered DNA structures have been proposed as mimics to ECM scaffolds. However, these principles have not been applied to mineralized tissues. Here, we describe DNA nanostructures, namely, a DNA nanotube and a DNA origami rectangle that are site specifically functionalized with a mineral-promoting "SSEE" peptide derived from ECM proteins present in mineralized tissues. In the presence of Ca2+ and phosphate ions (mineralizing conditions), site-specific calcium phosphate formation occurred on the DNA nanostructures. Amorphous calcium phosphate or hydroxyapatite was formed depending on the incubation time, shape of the DNA nanostructure, and amount of Ca2+ and phosphate ions present. The ability to design and control the growth of hydroxyapatite through nanoengineered scaffolds provides insights into the mechanisms that may occur during crystal nucleation and growth of mineralized tissues and can inspire mineralized tissue regeneration strategies.
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