Probing the Cellular Fate of the Protein Corona around Nanoparticles with Nanofocused X-ray Fluorescence Imaging

被引:2
|
作者
Skiba, Marvin [1 ,2 ]
Guedes, Gabriela [3 ]
Karpov, Dmitry [4 ]
Feliu, Neus [5 ]
L. Cortajarena, Aitziber [3 ,6 ]
Parak, Wolfgang J. [1 ,2 ]
Sanchez-Cano, Carlos [6 ,7 ,8 ]
机构
[1] Univ Hamburg, Ctr Hybrid Nanostruct, D-22761 Hamburg, Germany
[2] Hamburg Ctr Ultrafast Imaging, D-22761 Hamburg, Germany
[3] Basque Res & Technol Alliance BRTA, Ctr Cooperat Res Biomat CIC biomaGUNE, San Sebastian 20014, Spain
[4] European Synchrotron Radiat Facil, F-38000 Grenoble, France
[5] Fraunhofer Inst Angew Polymerforschung IAP, Zentrum Angew Nanotechnol CAN, D-20146 Hamburg, Germany
[6] Basque Fdn Sci, Ikerbasque, Bilbao 48009, Spain
[7] Donostia Int Phys Ctr, Donostia San Sebastian 20018, Spain
[8] Euskal Herriko Unibertsitatea UPV EHU, Polimero & Mat Aurreratuak Fis Kimika & Teknol, Kimika Fak, Donostia San Sebastian 20018, Spain
基金
欧洲研究理事会;
关键词
X-ray fluorescence imaging; nanoparticles; protein corona; intracellular fate; NANOPROBE BEAMLINE; GOLD NANOPARTICLES; COLOCALIZATION; TRANSFERRIN; TRAFFICKING; RECEPTOR; CELLS;
D O I
10.3390/ijms25010528
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
X-ray fluorescence imaging (XRF-imaging) with subcellular resolution is used to study the intracellular integrity of a protein corona that was pre-formed around gold nanoparticles (AuNP). Artificial proteins engineered to obtain Gd coordination for detection by XRF-imaging were used to form the corona. Indications about the degradation of this protein corona at a cellular and subcellular level can be observed by following the Au and Gd quantities in a time and spatial-dependent manner. The extended acquisition times necessary for capturing individual XRF-imaging cell images result in relatively small sample populations, stressing the need for faster image acquisition strategies in future XRF-imaging-based studies to deal with the inherent variability between cells. Still, results obtained reveal degradation of the protein corona during cellular trafficking, followed by differential cellular processing for AuNP and Gd-labelled proteins. Overall, this demonstrates that the dynamic degradation of the protein corona can be tracked by XRF-imaging to a certain degree.
引用
收藏
页数:16
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