开发用于抗耐甲氧西林金黄色葡萄球菌(MRSA)的三重螺旋重组胶原-银混合纳米纤维。

Caihong Fu, Jianrui Ma, Guangyu Liu, Yirui Fan, Nannan Wei, Jianxi Xiao
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引用次数: 0

摘要

医疗保健相关感染的威胁不断升级,这凸显了人们对生物相容性抗菌材料的迫切需求,这种材料能有效对抗耐药病原体。在这项研究中,我们提出了一种新颖的三螺旋重组胶原蛋白-银混合纳米纤维的制造方法,专门用于抗耐甲氧西林金黄色葡萄球菌(MRSA)。利用银介导的交联策略,我们利用 38 W 的低功率灯管使银离子(Ag+)介导各种蛋白质的交联。机理研究揭示了九个氨基酸在促进这一反应中的关键作用。三螺旋重组胶原蛋白(THRC)保持了其原生结构,形成了有序的纳米纤维,而其他球状蛋白质则形成了独特的网状结构。THRC 还是一种还原剂和分散剂,有助于在纳米纤维内原位合成高度分散的银纳米粒子 (AgNPs)(直径约为 7 纳米)。对 THRC 和 Ag+ 反应条件的系统研究表明,这种新方法在纳米纤维制造方面具有多功能性。AgNPs 的加入使 THRC/AgNPs 纳米纤维具有卓越的抗菌活性,对 MRSA 的最小抑菌浓度 (MIC) 为 19.2 mg/L,最小杀菌浓度 (MBC) 为 153.6 mg/L。这种创新方法为开发基于蛋白质的抗菌生物材料提供了巨大潜力,可用于伤口愈合和其他生物医学应用中的感染控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of triple-helical recombinant collagen-silver hybrid nanofibers for anti-methicillin-resistantStaphylococcus aureus(MRSA) applications.

The escalating threat of healthcare-associated infections highlights the urgent need for biocompatible antibacterial materials that effectively combat drug-resistant pathogens. In this study, we present a novel fabrication method for triple-helical recombinant collagen (THRC)-silver hybrid nanofibers, specifically designed for anti-methicillin-resistantstaphylococcus aureus(MRSA) applications. Utilizing a silver-mediated crosslinking strategy, we harness a low-power 38 W lamp to enable silver ions (Ag+) to mediate crosslinking across various proteins. Mechanistic insights reveal the pivotal role of nine amino acids in facilitating this reaction. The THRC maintains its native structure, forming well-ordered nanofibers, while other globular proteins form a distinctive network-like structure. THRC also serves as a reducing and dispersing agent, facilitating thein situsynthesis of highly dispersed silver nanoparticles (AgNPs) (∼7 nm in diameter) within the nanofibers. Systematic investigation of the reaction conditions between THRC and Ag+demonstrates the versatility of this novel approach for nanofiber fabrication. The incorporation of AgNPs imparts exceptional antibacterial activity to the THRC/AgNPs nanofibers, exhibiting a minimum inhibitory concentration of 19.2 mg l-1and a minimum bactericidal concentration of 153.6 mg l-1against MRSA. This innovative approach holds significant potential for developing antibacterial protein-based biomaterials for infection management in wound healing and other biomedical applications.

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