Hunan Provincial Key Laboratory of Cytochemistry, School of Chemistry and Biological Engineering, Changsha University of Science and Technology, Changsha, 410114, China.
Department of Chemistry, Waterloo Institute for Nanotechnology, University of Waterloo, Waterloo, Ontario, N2L 3G1, Canada.
Angew Chem Int Ed Engl. 2020 Aug 10;59(33):14044-14048. doi: 10.1002/anie.202003964. Epub 2020 Jun 3.
The Au-S bond is the classic way to functionalize gold nanoparticles (AuNPs). However, cleavage of the bond by biothiols and other chemicals is a long-standing problem hindering practical applications, especially in cells. Instead of replacing the thiol by a carbene or selenol for stronger adsorption, it is now shown that the Pt-S bond is much more stable, fully avoiding cleavage by biothiols. AuNPs were deposited with a thin layer of platinum, and an AuNP@Pt-S nanoflare was constructed to detect the miRNA-21 microRNA in living cells. This design retained the optical and cellular uptake properties of DNA-functionalized AuNPs, while showing high-fidelity signaling. It discriminated target cancer cells even in a mixed-cell culture system, where the Au-S based nanoflare was less sensitive. Compared to previous methods of changing the ligand chemistry, coating a Pt shell is more accessible, and previously developed methods for AuNPs can be directly adapted.
金-硫(Au-S)键是将金纳米颗粒(AuNPs)功能化的经典方法。然而,生物硫醇和其他化学物质对键的断裂是阻碍实际应用的长期存在的问题,特别是在细胞中。为了避免生物硫醇的断裂,人们不再通过卡宾或硒醇取代硫醇以获得更强的吸附,而是现在表明,Pt-S 键更加稳定,完全避免了生物硫醇的断裂。AuNPs 沉积有一层薄薄的铂,构建了 AuNP@Pt-S 纳米耀斑来检测活细胞中的 miRNA-21 微 RNA。该设计保留了 DNA 功能化 AuNPs 的光学和细胞摄取特性,同时表现出高保真信号。即使在混合细胞培养系统中,它也能区分靶癌细胞,而基于 Au-S 的纳米耀斑的灵敏度较低。与改变配体化学的先前方法相比,涂覆 Pt 壳更容易,并且可以直接采用先前开发的 AuNPs 方法。