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Peptide-directed preparation and X-ray structural study of au nanoparticles on titanium surfaces

机译:钛表面金纳米颗粒的肽导向制备及X射线结构研究

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We report the peptide-directed preparation and X-ray structural study of biofunctionalized Au nanoparticles (NPs) deposited on Ti surfaces. Au NPs were prepared by reduction of Au~(3+) compound onto HCl-refreshed Ti in the presence of thiol-functionalized small peptides. A modified extended X-ray absorption fine-structure (EXAFS) technique, equipped with a rotating-stage and glancing-angle setup, was able to more sensitively detect the structure and bonding of Au NPs on Ti with low surface coverage. It was found that the use of the tripeptide glutathione (GSH) results in smaller NP size when compared to N-(2-mercapto-propionyl) glycine (MPG), a pseudodipeptide, over a wide range of Au/peptide molar ratios (20:1, 10:1, 5:1, and 2:1). By varying the ligand concentration, the Au NP structure in both systems can be controlled, generating nanocrystals, nanoclusters, and Au-thiolate polymer, which is unique for substrate-supported NP synthesis. This work presents a facile preparation of Au-peptide nanoparticles on biocompatible surfaces, and illustrates the high sensitivity of this modified EXAFS technique for structural studies of substrate-supported nanoparticles with low coverage.
机译:我们报告了沉积在钛表面的生物功能化金纳米粒子(NPs)的肽指导的制备和X射线结构研究。通过在硫醇官能化的小肽存在下,将Au〜(3+)化合物还原到HCl还原的Ti上制备Au NP。改进的扩展X射线吸收精细结构(EXAFS)技术,配备了旋转台和掠角设置,能够更敏感地检测表面覆盖率低的Ti上Au NP的结构和键。发现在较宽的金/肽摩尔比范围内,与N-(2-巯基-丙酰基)甘氨酸(MPG)(一种伪二肽)相比,使用三肽谷胱甘肽(GSH)导致NP尺寸更小(20 :1、10:1、5:1和2:1)。通过改变配体浓度,可以控制两个系统中的Au NP结构,生成纳米晶体,纳米团簇和Au-thiolate聚合物,这对于底物支持的NP合成而言是独特的。这项工作提出了在生物相容性表面上的金-肽纳米颗粒的一种简便的制备方法,并说明了这种改良的EXAFS技术对低覆盖率的基质支撑纳米颗粒的结构研究具有很高的敏感性。

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