纳米颗粒
表面改性
生物流体
生物物理学
纳米毒理学
蛋白质组学
纳米技术
化学
纳米生物技术
血液蛋白质类
日冕(行星地质学)
材料科学
色谱法
生物化学
生物
物理化学
天体生物学
基因
维纳斯
作者
Stefan Tenzer,Dominic Docter,Jörg Kuharev,Anna Musyanovych,Verena Fetz,Rouven Hecht,Florian Schlenk,Dagmar Fischer,Klytaimnistra Kiouptsi,Christoph Reinhardt,Katharina Landfester,Hansjörg Schild,Michael Maskos,Shirley K. Knauer,Roland H. Stauber
标识
DOI:10.1038/nnano.2013.181
摘要
In biological fluids, proteins bind to the surface of nanoparticles to form a coating known as the protein corona, which can critically affect the interaction of the nanoparticles with living systems. As physiological systems are highly dynamic, it is important to obtain a time-resolved knowledge of protein-corona formation, development and biological relevancy. Here we show that label-free snapshot proteomics can be used to obtain quantitative time-resolved profiles of human plasma coronas formed on silica and polystyrene nanoparticles of various size and surface functionalization. Complex time- and nanoparticle-specific coronas, which comprise almost 300 different proteins, were found to form rapidly (<0.5 minutes) and, over time, to change significantly in terms of the amount of bound protein, but not in composition. Rapid corona formation is found to affect haemolysis, thrombocyte activation, nanoparticle uptake and endothelial cell death at an early exposure time.
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