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Protein corona of metal-organic framework nanoparticals: Study on the adsorption behavior of protein and cell interaction.

Authors :
Gan, Na
Sun, Qiaomei
Zhao, Ludan
Tang, Peixiao
Suo, Zili
Zhang, Shuangshuang
Zhang, Yongkui
Zhang, Man
Wang, Wenjing
Li, Hui
Source :
International Journal of Biological Macromolecules. Nov2019, Vol. 140, p709-718. 10p.
Publication Year :
2019

Abstract

Nanoscale metal–organic frameworks (NMOFs) have attracted considerable attention for controlled drug delivery. However, the interaction between nanoparticles and the biological macromolecules of physiological system must be valued because the formed protein corona will endow NMOFs with new biorecognition properties. In this study, we carried out detailed protein adsorption studies in vitro and cell uptake tests of HeLa cells for nanospherical Uio66 and nanooctahedral Uio67. Uio67 with higher binding constants to human serum albumin needed to combine more protein molecules to achieve colloidal stability state than that needed by Uio66, and this phenomenon led Uio67 to aggregate under the same incubation condition due to the formation of a single-layer protein. Uio67 also induced an evident conformation change in protein to stabilize the combination. In particular, the cell uptake efficiencies of the two systems showed a significant thickness dependence on the protein corona. When samples incubated in 10% fetal bovine serum (FBS), the intracellular rate was the highest for both systems, but the rate was not proportional to the FBS concentration. Results of this work are important to the development of the considerable potential NMOFs-based medicals and also provide additional insight into protein corona. Unlabelled Image • Distinct morphologies impacted on surface chemistry and cell uptake differently. • Cell uptake efficiencies showed thickness dependence on the protein corona. • Uio67 needed to combine more protein to achieve the colloidal stability state • HSA experienced different degrees conformation change to stabilize the combination. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01418130
Volume :
140
Database :
Academic Search Index
Journal :
International Journal of Biological Macromolecules
Publication Type :
Academic Journal
Accession number :
140232742
Full Text :
https://doi.org/10.1016/j.ijbiomac.2019.08.183