纳米颗粒仿生功能材料(演示记录)

K. Ijiro
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引用次数: 0

摘要

自组装起源于分子,从自然到非自然系统都无处不在。DNA、病毒、分子晶体、脂质体等双链结构的形成都是分子自组装的实例。例如,在生物系统中,病毒是一项令人印象深刻的分子工程壮举,它通过弱疏水效应将数百种蛋白质组装在一起。我们提出了一种强大的策略,通过碳水化合物端端氟化表面配体与5~40nm的AuNPs自组装,制备由金纳米颗粒代替蛋白质组成的仿生病毒纳米结构的金纳米颗粒囊泡(aunv),表明碳水化合物可以作为比低聚乙二醇更强的分子胶。引入碳水化合物,通过改变葡萄糖(即葡萄糖、麦芽糖和麦芽糖)的数量来调节配体的亲水性。通过改变表面配体、二氧六环中的水含量和AuNPs的大小,可以有效地控制AuNPs的大小。我们发现由30纳米金纳米颗粒组成的VLPs和unvs有一些相似之处。不仅测量了aunv的光子特性,还测量了其他自组装纳米粒子的光子特性。在纳米金纳米颗粒和自组装金纳米颗粒中检测到分子的强表面增强拉曼散射(SERS)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nanoparticle-based biomimetic functional materials (Presentation Recording)
Self-assembly originated from molecules, is ubiquitous from nature to unnature systems. The formation of double-stranded structure of DNA, virus, molecular crystals, liposomes etc. are all instances of molecular self-assembly. In the biological system, for example, virus is an impressive feat of molecular engineering by assembly of hundreds of proteins through the weak hydrophobic effect. We propose a robust strategy for the size-controllable fabrication of gold nanoparticle vesicles(AuNVs) which are biomimetic nanostructures of virus consisted of gold nanoparticles instead of proteins by using carbohydrate terminated fluorinated surface ligand self-assembly with 5~40nm AuNPs, indicating that carbohydrate can act as stronger molecular glue than oligo(ethylene glycol). Carbohydrate was introduced to tune the hydrophilic effect of the ligand by varying the number of glucose (namely, glucose, maltose, and maltotriose). AuNVs size could be efficiently controlled by varying surface ligands, water content in dioxane, and AuNPs size. We find some similarities between VLPs and AuNVs composed of 30nm gold nanoparticles. Photonic properties of not only AuNVs but also other self-assemblies of nanoparticles were measured. Strong surface-enhanced Raman scattering (SERS) of molecules were detected from the AuNVs and self-assembled gold nanoparticles.
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