Department of Materials Technology and Chemistry, Faculty of Chemistry, University of Lodz, Pomorska 163, 90-236 Lodz, Poland.
Department of Genetics, Plant Molecular Biology and Biotechnology, Faculty of Biology and Environmental Protection, University of Lodz, Banacha 12/16, 90-237 Lodz, Poland.
Colloids Surf B Biointerfaces. 2017 Nov 1;159:533-539. doi: 10.1016/j.colsurfb.2017.08.019. Epub 2017 Aug 18.
In this study we present a method to determine the degree to which catalase (CAT) is adsorbed onto gold nanoparticles (AuNPs) using polyacrylamide gel electrophoresis (PAGE) with silver staining. AuNPs (13nm) were synthesized in water by the chemical reduction method and modified with CAT (AuNPs-CAT). The colloidal stability and NP size before and after the modification were investigated by dynamic light scattering and scanning transmission electron microscopy. Electrophoresis was performed under different conditions (native, with and without SDS, and with and without β-mercaptoethanol) to find the optimal conditions for determining the surface coverage of AuNPs with CAT protein. The results clearly indicate that PAGE can be used to determine the amount of protein adsorbed on the NP surface and the use of native PAGE does not alter the colloidal stability of the NPs. These features allowed us to monitor the state of NPs and protein-NP interactions during the electrophoretic process.
在这项研究中,我们提出了一种使用聚丙烯酰胺凝胶电泳(PAGE)结合银染来确定过氧化氢酶(CAT)在金纳米粒子(AuNPs)上吸附程度的方法。AuNPs(13nm)通过化学还原法在水中合成,并通过 CAT(AuNPs-CAT)进行修饰。通过动态光散射和扫描透射电子显微镜研究了修饰前后胶体的稳定性和 NP 尺寸。在不同条件下(天然、有和没有 SDS、有和没有β-巯基乙醇)进行电泳,以找到确定 CAT 蛋白在 AuNPs 表面覆盖率的最佳条件。结果清楚地表明,PAGE 可用于确定吸附在 NP 表面的蛋白质的量,并且使用天然 PAGE 不会改变 NPs 的胶体稳定性。这些特性使我们能够在电泳过程中监测 NPs 的状态和蛋白质-NP 相互作用。