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柠檬酸盐稳定的金纳米颗粒中尺寸依赖性蛋白质-纳米颗粒相互作用:蛋白质冠层的出现

Size-Dependent Protein-Nanoparticle Interactions in Citrate-Stabilized Gold Nanoparticles: The Emergence of the Protein Corona.

作者信息

Piella Jordi, Bastús Neus G, Puntes Víctor

机构信息

Institut Català de Nanociència i Nanotecnologia (ICN2), CSIC and The Barcelona Institute of Science and Technology (BIST) , Campus UAB, 08193, Bellaterra, Barcelona, Spain.

Universitat Autònoma de Barcelona (UAB) , Campus UAB, 08193 Bellaterra, Barcelona, Spain.

出版信息

Bioconjug Chem. 2017 Jan 18;28(1):88-97. doi: 10.1021/acs.bioconjchem.6b00575. Epub 2016 Dec 20.

Abstract

Surface modifications of highly monodisperse citrate-stabilized gold nanoparticles (AuNPs) with sizes ranging from 3.5 to 150 nm after their exposure to cell culture media supplemented with fetal bovine serum were studied and characterized by the combined use of UV-vis spectroscopy, dynamic light scattering, and zeta potential measurements. In all the tested AuNPs, a dynamic process of protein adsorption was observed, evolving toward the formation of an irreversible hard protein coating known as Protein Corona. Interestingly, the thickness and density of this protein coating were strongly dependent on the particle size, making it possible to identify different transition regimes as the size of the particles increased: (i) NP-protein complexes (or incomplete corona), (ii) the formation of a near-single dense protein corona layer, and (iii) the formation of a multilayer corona. In addition, the different temporal patterns in the evolution of the protein coating came about more quickly for small particles than for the larger ones, further revealing the significant role that size plays in the kinetics of this process. Since the biological identity of the NPs is ultimately determined by the protein corona and different NP-biological interactions take place at different time scales, these results are relevant to biological and toxicological studies.

摘要

研究了尺寸范围为3.5至150nm的高度单分散柠檬酸盐稳定的金纳米颗粒(AuNP)在暴露于补充有胎牛血清的细胞培养基后的表面修饰,并通过紫外可见光谱、动态光散射和zeta电位测量的联合使用进行了表征。在所有测试的AuNP中,均观察到蛋白质吸附的动态过程,该过程朝着形成称为蛋白质冠的不可逆硬蛋白质涂层发展。有趣的是,这种蛋白质涂层的厚度和密度强烈依赖于颗粒大小,这使得随着颗粒尺寸的增加可以识别不同的转变状态:(i)NP-蛋白质复合物(或不完全冠),(ii)形成近乎单一的致密蛋白质冠层,以及(iii)形成多层冠。此外,小颗粒比大颗粒的蛋白质涂层演变中的不同时间模式出现得更快,这进一步揭示了尺寸在该过程动力学中所起的重要作用。由于NP的生物学特性最终由蛋白质冠决定,并且不同的NP-生物相互作用在不同的时间尺度上发生,因此这些结果与生物学和毒理学研究相关。

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