基于γ- aapep肽的抗菌肽模拟物作为耐药细菌潜在治疗手段的研究进展。

Exploration of drug science Pub Date : 2025-01-01 Epub Date: 2025-02-19 DOI:10.37349/eds.2025.100888
Jarais Fontaine, Jianfeng Cai
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引用次数: 0

摘要

在过去60年里,只引进了四种新的抗生素,而耐药革兰氏阳性和革兰氏阴性细菌的流行率却有所上升。这强调了迫切需要新的抗菌疗法。这篇评论利用了最近对γ-取代- n -酰基化- n -氨基乙基氨基酸肽(γ-AApeptides)的探索来模拟天然抗菌肽(amp)的结构和功能,强调了开发新的有效治疗抗生素耐药细菌的希望和局限性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Recent exploration of γ-AApeptide based antimicrobial peptide mimics as potential therapeutics towards drug-resistant bacteria.

Recent exploration of γ-AApeptide based antimicrobial peptide mimics as potential therapeutics towards drug-resistant bacteria.

Recent exploration of γ-AApeptide based antimicrobial peptide mimics as potential therapeutics towards drug-resistant bacteria.

Over the last 60 years, only four new classes of antibiotics have been introduced, while the prevalence of antibiotic-resistant Gram-positive and Gram-negative bacteria has risen. This underscores the urgent need for new antibacterial therapeutics. This commentary leverages the recent exploration of γ-substituted-N-acylated-N-aminoethyl amino acid peptides (γ-AApeptides) to mimic the structures and function of natural antimicrobial peptides (AMPs), highlighting the promise and limitations for developing a new, effective treatment for antibiotic-resistant bacteria.

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