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Nanoscale reorganizations of histone-like nucleoid structuring proteins in Escherichia coli are caused by silver nanoparticles

机译:大肠杆菌中组蛋白样核结构蛋白的纳米级重组是由银纳米颗粒引起的

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Silver nanoparticles (AgNPs) and ions (Ag+) have recently gained broad attention due to their antimicrobial effects against bacteria and other microbes. In this work, we demonstrate the use of super-resolution fluorescence microscopy for investigating and quantifying the antimicrobial effect of AgNPs at the molecular level. We found that subjecting Escherichia coli (E. coli) bacteria to AgNPs led to nanoscale reorganization of histone-like nucleoid structuring (H-NS) proteins, an essential nucleoid associated protein in bacteria. We observed that H-NS proteins formed denser and larger clusters at the center of the bacteria after exposure to AgNPs. We quantified the spatial reorganizations of H-NS proteins by examining the changes of various spatial parameters, including the inter-molecular distances and molecular densities. Clustering analysis based on Voronoi-tessellation were also performed to characterize the change of H-NS proteins' clustering behavior. We found that AgNP-treatment led to an increase in the fraction of H-NS proteins forming clusters. Similar effects were observed for bacteria exposed to Ag+ ions, suggesting that the release of Ag+ ions plays an important role in the toxicity of AgNPs. On the other hand, we observed that AgNPs with two surface coatings showed difference in the nanoscale reorganization of H-NS proteins, indicating that particle-specific effects also contribute to the antimicrobial activities of AgNPs. Our results suggested that H-NS proteins were significantly affected by AgNPs and Ag+ ions, which has been overlooked previously. In addition, we examined the dynamic motion of AgNPs that were attached to the surface of bacteria. We expect that the current methodology can be readily applied to broadly and quantitatively study the spatial reorganization of biological macromolecules at the scale of nanometers caused by metal nanoparticles, which are expected to shed new light on the antimicrobial mechanism of metal nanoparticles.
机译:由于它们对细菌和其他微生物的抗微生物作用,最近,银纳米颗粒(AgNPS)和离子(Ag +)最近受到广泛。在这项工作中,我们证明了使用超分辨率的荧光显微镜检查来研究和量化分子水平AgNP的抗微生物效果。我们发现将大肠杆菌(大肠杆菌)细菌对AGNPS导致纳米级核心核构造(H-NS)蛋白,细菌中必需的核心相关蛋白质的纳米级重组。我们观察到H-NS蛋白在暴露于AgNP后在细菌的中心形成密集和更大的簇。我们通过检查各种空间参数的变化来量化H-NS蛋白的空间重组,包括分子间距离和分子密度。还进行了基于voronoi-tessellation的聚类分析,以表征H-NS蛋白的聚类行为的变化。我们发现AGNP治疗导致H-NS蛋白形成簇的级分的增加。对于暴露于Ag +离子的细菌,观察到类似的效果,表明Ag +离子的释放在agnps的毒性中起重要作用。另一方面,我们观察到具有两个表面涂层的AgNP显示出H-NS蛋白的纳米级重组的差异,表明颗粒特异性效应也有助于AgNP的抗微生物活性。我们的结果表明,H-NS蛋白受到agnps和Ag +离子的显着影响,此前已经忽略过。此外,我们检查了附着在细菌表面上的AgNP的动态运动。我们预计,目前的方法可以容易地应用于在引起金属纳米颗粒,其被预期在金属纳米粒子的抗菌机理棚新光纳米尺度广泛地和定量研究生物大分子的空间重组。

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