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Effects of protein species and surface physicochemical features on the deposition of nanoparticles onto protein-coated planar surfaces

机译:蛋白质物种和表面物理化学特征对纳米粒子沉积到蛋白质涂层平面表面的影响

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摘要

Proteins are often an important component of many bulk surfaces in biological and environmental systems that are coated with complex organic compounds that may also interact with NPs. We investigated the deposition of bare hematite NPs onto various proteins adsorbed on either negatively-or positively-charged bottom surfaces. Bovine serum albumin (BSA), lysozyme, and ubiquitin were used as model proteins and total protein extracts from two bacterial strains, Escherichia coli and Pseudomonas fluorescens, were used as complex protein mixtures. The NP deposition extents and rates were shown to be significantly different depending on the protein. The maximum difference observed was 8.6 +/- 3.2 fold between E. coli and P. fluorescens proteins adsorbed onto positively-charged planar surfaces. These differences in NP deposition characteristics are attributed to the differences in physicochemical features of the topmost surface of the protein layer, such as the amino acid profiles, surface charge, and hydrophilicity. Such differences were likely driven by differences in species, orientation, and conformation of the adsorbed proteins. In particular, NP deposition was driven by various combinations of electrostatic and hydrophobic interactions. This study indicates that NP deposition onto surface-adsorbed proteins is an important mechanism in protein-NP interactions and that the deposition is strongly dependent on both the conformation and chemical characteristics of the adsorbed protein layer.
机译:蛋白质通常是许多散装表面的重要组成部分,其生物和环境系统中涂有复杂的有机化合物,也可以与NPS相互作用。我们研究了裸露的赤铁矿NP沉积在吸附在负电或带正电的底表面上的各种蛋白质上。牛血清白蛋白(BSA),溶菌酶和泛素用作模型蛋白质,并用两种细菌菌株,大肠杆菌和假单胞菌的总蛋白质提取物用作复合蛋白质混合物。根据蛋白质,显示NP沉积范围和速率明显不同。观察到的最大差异为8.6 +/- 3.2折叠在大肠杆菌和P.吸附在带正电的平面表面上的荧光蛋白。 NP沉积特性的这些差异归因于蛋白质层最顶表面的物理化学特征的差异,例如氨基酸谱,表面电荷和亲水性。这种差异可能是由吸附蛋白质的物种,取向和构象的差异驱动。特别地,通过各种静电和疏水相互作用的组合驱动NP沉积。该研究表明,NP沉积在表面吸附的蛋白质上是蛋白质-NP相互作用的重要机制,并且沉积强烈取决于吸附蛋白质层的构象和化学特性。

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  • 来源
    《RSC Advances》 |2016年第79期|共8页
  • 作者单位

    Baylor Univ Dept Geol Waco TX 76798 USA;

    Univ Texas Dallas Dept Mat Sci &

    Engn Richardson TX 75080 USA;

    Univ Texas Dallas Dept Mat Sci &

    Engn Richardson TX 75080 USA;

    Baylor Univ Dept Geol Waco TX 76798 USA;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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