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Conformational-transited protein corona regulated cell-membrane penetration and induced cytotoxicity of ultrasmall Au nanoparticles.

作者信息

Yang Huayan, Wang Meng, Zhang Yanmin, Li Feng, Yu Shaoning, Zhu Lin, Guo Yuming, Yang Lin, Yang Shouning

机构信息

Key Laboratory of Green Chemical Media and Reactions, School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Ministry of Education, Henan Normal University Xinxiang People's Republic of China

University of Shanghai for Science and Technology Shanghai People's Republic of China.

出版信息

RSC Adv. 2019 Feb 5;9(8):4435-4444. doi: 10.1039/c8ra10049g. eCollection 2019 Jan 30.


DOI:10.1039/c8ra10049g
PMID:35520163
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9060578/
Abstract

Nanoparticles (NP) in biological fluids almost invariably become coated with proteins to form protein coronas. It is the NP-protein corona rather than the bare nanoparticle that determines the nanoparticle's bio-behavior. Here, ultrasmall gold nanoparticles (AuNPs) coated by a human serum albumin (HSA) corona were studied by Fourier transform infrared spectroscopy, denature experiments, fluorescence quenching. Moreover, the intracellular fate of AuNPs and the AuNP-HSA corona has also been investigated. The results show that HSA corona undergo a conformational transition (partial β-sheet changed to α-helicity) when they adsorb on AuNPs, which lead to an enhanced thermal stability. Importantly, we observed that the conformation-transited protein corona-AuNP complex could induce cell apoptosis. Meanwhile, for the first time, the conformation-transited HSA on the AuNPs surface are shown to disrupt living cell membranes. The results obtained here not only provide the detailed conformational behavior of HSA molecules on nanoparticles, but also reveal the structure-function relationship of protein corona, which is of utmost importance in the safe application of nanoscale objects in living organisms.

摘要

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[2]
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[3]
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[4]
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[5]
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[6]
Biomolecular interactions of ultrasmall metallic nanoparticles and nanoclusters.

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[7]
Impact of particle size and pH on protein corona formation of solid lipid nanoparticles: A proof-of-concept study.

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[8]
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[9]
Insights into Characterization Methods and Biomedical Applications of Nanoparticle-Protein Corona.

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本文引用的文献

[1]
Nanoparticle Ligand Exchange and Its Effects at the Nanoparticle-Cell Membrane Interface.

Nano Lett. 2018-10-18

[2]
Modulation of Fluorescent Protein Chromophores To Detect Protein Aggregation with Turn-On Fluorescence.

J Am Chem Soc. 2018-6-12

[3]
Translating Current Bioanalytical Techniques for Studying Corona Activity.

Trends Biotechnol. 2018-4-27

[4]
A Decade of the Protein Corona.

ACS Nano. 2017-12-5

[5]
Plasma protein adsorption and biological identity of systemically administered nanoparticles.

Nanomedicine (Lond). 2017-8-14

[6]
AgHalo: A Facile Fluorogenic Sensor to Detect Drug-Induced Proteome Stress.

Angew Chem Int Ed Engl. 2017-6-19

[7]
Nanomedicine: Evolution of the nanoparticle corona.

Nat Nanotechnol. 2017-4-6

[8]
Probing the binding affinity of plasma proteins adsorbed on Au nanoparticles.

Nanoscale. 2017-4-6

[9]
Regimes of Biomolecular Ultrasmall Nanoparticle Interactions.

Angew Chem Int Ed Engl. 2017-3-15

[10]
The Impact of Protein Corona Formation on the Macrophage Cellular Uptake and Biodistribution of Spherical Nucleic Acids.

Small. 2017-2-14

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