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丁香酸导向合成金纳米簇及其在定量基质辅助激光解吸/电离质谱中的应用。

Sinapinic acid-directed synthesis of gold nanoclusters and their application to quantitative matrix-assisted laser desorption/ionization mass spectrometry.

机构信息

Department of Chemistry, National Sun Yat-sen University, Kaohsiung, Taiwan.

出版信息

Nanoscale. 2014;6(3):1347-53. doi: 10.1039/c3nr04991d.

DOI:10.1039/c3nr04991d
PMID:24288017
Abstract

Core etching of gold nanoparticles (AuNPs) into smaller-sized clusters is a classic method for fabricating gold nanoclusters (AuNCs). The top down-based synthesis of AuNCs includes two steps: (i) reducing the Au(3+) precursor solution to generate AuNPs in the presence of protecting ligands and (ii) core etching of the formed AuNPs into the AuNCs via ligand exchange. For the first time, this paper describes a one-step approach for preparing AuNCs using a top down approach. The sinapinic acid (SA)-induced formation of the AuNCs involved a three-step reaction process. First, large AuNPs (>200 nm) were quickly formed after mixing SA and the Au(3+) precursor solution. Second, excess SA molecules self-assembled on the NP surface, and large AuNPs were etched to small AuNPs via electrostatic repulsion between the neighboring SA molecules. Finally, SA-induced core etching of the AuNPs resulted in the formation of the AuNCs within 70 min. Furthermore, we showed that the presence of the AuNCs in SA was capable of suppressing crystal growth and eliminating the coffee-ring effect. Thus, proteins can be successfully quantified using the SA-AuNCs as matrices for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. Compared with using SA as matrices, the SA-AuNCs offered substantial advantages for improving shot-to-shot reproducibility and enhancing the ionization efficiency of proteins.

摘要

金纳米粒子 (AuNPs) 的核心刻蚀成更小尺寸的团簇是制备金纳米团簇 (AuNCs) 的经典方法。基于自上而下的 AuNCs 合成包括两个步骤:(i) 在保护配体存在的情况下还原 Au(3+) 前体溶液以生成 AuNPs,和 (ii) 通过配体交换将形成的 AuNPs 核心刻蚀成 AuNCs。本文首次描述了一种使用自上而下方法一步制备 AuNCs 的方法。金纳米团簇的合成涉及三个反应步骤。首先,混合金纳米团簇和 Au(3+) 前体溶液后,快速形成大的 AuNPs (>200nm)。其次,过量的 SA 分子在 NP 表面自组装,由于相邻 SA 分子之间的静电排斥作用,大的 AuNPs 被刻蚀成小的 AuNPs。最后,SA 诱导的 AuNPs 核心刻蚀导致在 70 分钟内形成 AuNCs。此外,我们表明,在 SA 中存在 AuNCs 能够抑制晶体生长并消除咖啡环效应。因此,可以使用 SA-AuNCs 作为基质进行基质辅助激光解吸/电离飞行时间质谱法来成功定量蛋白质。与使用 SA 作为基质相比,SA-AuNCs 为提高蛋白质的单次测量重现性和增强其离子化效率提供了显著优势。

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