López-Olivos Juan Carlos, Álvarez-García Andrés, Garza Ramos Georgina, Huerta Lázaro, Molina Paola, Heredia-Barbero Alejandro, Garzón Ignacio L, Rodríguez-Zamora Penélope
Instituto de Física, Universidad Nacional Autónoma de México Apartado Postal 20-364 Ciudad de México 01000 Mexico
Facultad de Medicina, Universidad Nacional Autónoma de México Av. Universidad 3000 Ciudad de México 04510 Mexico.
Nanoscale Adv. 2025 Mar 12;7(9):2648-2662. doi: 10.1039/d5na00208g. eCollection 2025 Apr 29.
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.
谷胱甘肽(GSH)在众多生理和代谢过程中发挥着关键作用,包括保护细胞免受自由基和金属毒性的影响。这种三肽已与多种金属纳米颗粒结合,形成具有独特性质的金属-有机界面。在此,我们采用一步高产合成方法,制备尺寸介于尺寸选择纳米团簇和等离子体纳米颗粒之间的超小金、银和铜纳米颗粒,并用L-和D-谷胱甘肽进行功能化,研究每种情况下出现的光学活性所证明的手性转移。每种金属在金属-配体界面发生的独特相互作用主要决定了该系统的性质。在其质子化状态下,谷胱甘肽仅通过其硫醇基团锚定在金和铜纳米颗粒的表面,而对于银纳米颗粒,XPS数据表明通过酰胺基团的氮原子存在额外的结合位点,尽管比例相对较低。这可能导致在银-谷胱甘肽纳米颗粒中观察到更高的各向异性因子。吸附构型的这种微小变化产生了不同的手性光学活性,已使用含时密度泛函理论计算按能量区域进行了分析,结果表明金属到配体的跃迁主导了大部分光谱,而配体到配体的跃迁也出现在较高能量区域。此外,FTIR和CD数据共同表明,这些差异还通过每种金属分子间的GSH相互作用促进了特定的肽自组装,从而形成具有β-折叠阵列性质的超分子结构。本研究对谷胱甘肽功能化的货币金属的手性进行了平行研究,从而确定了决定性差异,可加以调整以促进手性生物医学和其他各种应用的发展。