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d-半胱氨酸/聚乙二醇功能化金纳米粒子的抗菌机制及其在细菌感染治疗中的潜力。

Antibacterial Mechanism of d-Cysteine/Polyethylene Glycol-Functionalized Gold Nanoparticles and Their Potential for the Treatment of Bacterial Infections.

机构信息

National Center of Meat Quality & Safety Control, College of Food Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.

College of Food Science and Engineering, Collaborative Innovation Center for Modern Grain Circulation and Safety, Nanjing University of Finance and Economics, Nanjing 210023, China.

出版信息

ACS Appl Mater Interfaces. 2024 Jul 24;16(29):37722-37733. doi: 10.1021/acsami.4c07721. Epub 2024 Jul 13.

Abstract

Bacterial infection has always posed a severe threat to public health. Gold nanoparticles (Au NPs) exhibit exceptional biocompatibility and hold immense potential in biomedical applications. However, their antibacterial effectiveness is currently unsatisfactory. Herein, a chiral antibacterial agent with high stability was prepared by the modification of Au NPs with d-cysteine with the assistance of polyethylene glycol (PEG). The as-synthesized d-cysteine/PEG-Au NPs (D/P-Au NPs) exhibited a stronger (99.5-99.9%) and more stable (at least 14 days) antibacterial performance against Gram-negative ( and ) and Gram-positive ( and ) bacteria, compared with other groups. The analysis of the antibacterial mechanism revealed that the D/P-Au NPs mainly affected the assembly of ribosomes, the biosynthesis of amino acids and proteins, as well as the DNA replication and mismatch repair, ultimately leading to bacterial death, which is significantly different from the mechanism of reactive oxygen species-activated metallic antibacterial NPs. In particular, the D/P-Au NPs were shown to effectively accelerate the healing of -infected wounds in mice to a rate comparable to or slightly higher than that of vancomycin. This work provides a novel approach to effectively design chiral antibacterial agents for bacterial infection treatment.

摘要

细菌感染一直对公共卫生构成严重威胁。金纳米粒子(Au NPs)表现出非凡的生物相容性,在生物医学应用中具有巨大的潜力。然而,它们的抗菌效果目前并不令人满意。在此,我们通过 d-半胱氨酸与聚乙二醇(PEG)的协同作用对 Au NPs 进行修饰,制备了一种具有高稳定性的手性抗菌剂。所合成的 d-半胱氨酸/PEG-Au NPs(D/P-Au NPs)对革兰氏阴性菌(和)和革兰氏阳性菌(和)的抗菌性能更强(99.5-99.9%)且更稳定(至少 14 天),与其他组相比。抗菌机制分析表明,D/P-Au NPs 主要影响核糖体的组装、氨基酸和蛋白质的生物合成以及 DNA 的复制和错配修复,最终导致细菌死亡,这与活性氧激活的金属抗菌 NPs 的机制明显不同。特别是,D/P-Au NPs 被证明可以有效地加速感染伤口的愈合,其愈合速度与万古霉素相当或略高。这项工作为有效设计用于细菌感染治疗的手性抗菌剂提供了一种新方法。

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