Shang Li, Gao Peng, Wang Haixia, Popescu Radian, Gerthsen Dagmar, Nienhaus Gerd Ulrich
Institute of Applied Physics , Karlsruhe Institute of Technology (KIT) , 76131 Karlsruhe , Germany.
Institute of Nanotechnology , Karlsruhe Institute of Technology (KIT) , 76344 Eggenstein-Leopoldshafen , Germany.
Chem Sci. 2017 Mar 1;8(3):2396-2400. doi: 10.1039/c6sc04664a. Epub 2016 Dec 19.
Development of nanoparticles for super-resolution imaging (sriNPs) can greatly enrich the toolbox of robust optical probes for biological studies. Moreover, sriNPs enable us to monitor the behavior of engineered nanomaterials in complex biological environments with high spatial resolution, which is important for advancing our understanding of nano-bio interactions. Up to now, reports on sriNPs have been scarce. In this work, we report a facile strategy to prepare protein-based fluorescent NPs that can be utilized as probes in super-resolution microscopy. The method is simple and straightforward, and easily extendible to other types of fluorophores. By using Atto647N-transferrin NPs as an example, we have achieved a roughly four-fold resolution improvement by using STED nanoscopy. These protein-based sriNPs possess excellent biocompatibility, good colloidal stability and photostability, making them attractive candidates for biological studies. Moreover, STED nanoscopy enables the precise imaging of NP structures in living cells, and revealed the co-existence of multiple NPs within one endosomal vesicle.
用于超分辨率成像的纳米颗粒(sriNPs)的开发可以极大地丰富用于生物学研究的强大光学探针工具箱。此外,sriNPs使我们能够在复杂的生物环境中以高空间分辨率监测工程纳米材料的行为,这对于增进我们对纳米-生物相互作用的理解非常重要。到目前为止,关于sriNPs的报道很少。在这项工作中,我们报告了一种简便的策略来制备基于蛋白质的荧光纳米颗粒,该颗粒可作为超分辨率显微镜中的探针。该方法简单直接,并且易于扩展到其他类型的荧光团。以Atto647N-转铁蛋白纳米颗粒为例,我们通过使用受激发射损耗(STED)纳米显微镜实现了约四倍的分辨率提升。这些基于蛋白质的sriNPs具有出色的生物相容性、良好的胶体稳定性和光稳定性,使其成为生物学研究的有吸引力的候选者。此外,STED纳米显微镜能够对活细胞中的纳米颗粒结构进行精确成像,并揭示了一个内体囊泡中多个纳米颗粒的共存。