l-谷胱甘肽和d-谷胱甘肽手性转移到金、银和铜纳米粒子中的金属配体界面效应。

IF 4.6 3区 材料科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Juan Carlos López-Olivos, Andrés Álvarez-García, Georgina Garza Ramos, Lázaro Huerta, Paola Molina, Alejandro Heredia-Barbero, Ignacio L Garzón, Penélope Rodríguez-Zamora
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引用次数: 0

摘要

谷胱甘肽(GSH)在许多生理和代谢过程中起着关键作用,包括细胞防御自由基和金属毒性。这种三肽与几种金属纳米颗粒结合,形成具有独特性能的金属-有机界面。在这里,我们实现了一种一步、高产率的合成方法,以生产超小的金、银和铜纳米颗粒,其大小介于尺寸选择的纳米团簇和被l-谷胱甘肽和d-谷胱甘肽功能化的等离子体纳米颗粒之间,并研究了每种情况下观察到的涌现光学活性所证明的手性转移。每种金属在金属-配体界面上发生的独特相互作用是建立该体系性质的主要原因。在质子化状态下,谷胱甘肽仅通过其硫基锚定在金纳米粒子和铜纳米粒子的表面,而对于银纳米粒子,XPS数据表明通过酰胺基的氮原子有额外的结合位点,尽管比例相对较低。这可能有助于在银谷胱甘肽纳米颗粒中观察到更高的各向异性因子。这种微小的吸附结构变化产生了不同的热交换活性,利用时间相关的DFT计算分析了每个能量区域,揭示了金属到配体的转变主导了大部分光谱,而配体到配体的转变也存在于更高的能量区域。此外,FTIR和CD数据共同表明,这些差异还通过分子间谷胱甘肽相互作用促进了每种金属的特定肽自组装,从而产生具有β -片阵列性质的超分子结构。本研究提供了对谷胱甘肽功能化铸币金属的手性的平行检查,允许建立决定性的差异,可以量身定制,有利于手性生物医学和其他不同应用的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Metal-ligand interface effect in the chirality transfer from l- and d-glutathione to gold, silver and copper nanoparticles.

Glutathione (GSH) plays a pivotal role in numerous physiological and metabolic processes, including the defense of cells against free radicals and metal toxicity. This tripeptide has been combined with several metal nanoparticles to form a metal-organic interface with unique properties. Here, we implement a one-step, high-yield synthesis method to produce ultrasmall gold, silver, and copper nanoparticles in the intermediate size regime between size-selected nanoclusters and plasmonic nanoparticles to be functionalized with l- and d-glutathione, and study the chirality transfer evidenced by the emergent optical activity observed for each case. The distinctive interactions that take place at the metal-ligand interface for each metal are primarily accountable for establishing the properties of this system. In its protonated state, glutathione anchors only by its thiol group to the surface of gold and copper nanoparticles, whilst for silver nanoparticles an additional binding site through the nitrogen atom of the amide group was indicated by XPS data, albeit with a relatively low proportion. This may contribute to the higher anisotropy factor observed in silver-glutathione nanoparticles. Such slight variations in adsorption configuration generate different chiroptical activity, which has been analyzed per energy region using time-dependent DFT calculations, revealing that metal-to-ligand transitions dominate most of the spectra while ligand-to-ligand are also present in the higher energy regime. Moreover, FTIR and CD data together suggest that those dissimilarities also propitiate particular peptide self-assemblies through intermolecular GSH interactions for each metal, which result in supramolecular structures with properties of beta-sheet arrays. This study offers a parallel examination of the chirality of glutathione-functionalized coinage metals, allowing to establish decisive differences that can be tailored to benefit developments in chiral biomedicine and other diverse applications.

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来源期刊
Nanoscale Advances
Nanoscale Advances Multiple-
CiteScore
8.00
自引率
2.10%
发文量
461
审稿时长
9 weeks
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