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构象转变的蛋白质冠层调节超小金纳米颗粒的细胞膜穿透并诱导其细胞毒性。

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.

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

生物流体中的纳米颗粒(NP)几乎总是会被蛋白质包裹,形成蛋白质冠层。决定纳米颗粒生物行为的是NP-蛋白质冠层,而非裸露的纳米颗粒。在此,通过傅里叶变换红外光谱、变性实验、荧光猝灭研究了由人血清白蛋白(HSA)冠层包裹的超小金纳米颗粒(AuNP)。此外,还研究了AuNP和AuNP-HSA冠层在细胞内的命运。结果表明,HSA冠层吸附在AuNP上时会发生构象转变(部分β-折叠转变为α-螺旋),这导致其热稳定性增强。重要的是,我们观察到构象转变的蛋白质冠层-AuNP复合物可诱导细胞凋亡。同时,首次表明AuNP表面构象转变的HSA会破坏活细胞膜。此处获得的结果不仅提供了HSA分子在纳米颗粒上的详细构象行为,还揭示了蛋白质冠层的结构-功能关系,这对于纳米级物体在活生物体中的安全应用至关重要。

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