化学
地氯酸
细菌
抗菌剂
生物化学
行动方式
细菌细胞结构
溶解循环
抗菌肽
肽
膜
合理设计
氨基酸
微生物学
组合化学
细胞膜
肽聚糖
肽序列
阳离子聚合
噬菌体展示
聚合物
细胞壁
抗生素
细胞
作者
Arunima Sandeep,Laila Zaatouf,Alexandre A. Arnold,Dror E. Warschawski,Isabelle Marcotte
摘要
Lytic antimicrobial peptides (AMPs) are long recognized for their ability to disrupt bacterial membranes, yet their interactions with other cell-envelope components remain poorly understood. Such knowledge is essential for redesigning AMPs as next-generation antibiotics or tailoring them for strain-specific activity. Here we show, using solid-state and solution NMR, that cationic AMPs engage directly with wall teichoic acids (WTAs)─anionic polymers in the Gram-positive bacteria cell wall. Three representative AMPs acting through different mode of membrane disruption display distinct binding to WTA phosphate groups. Solution NMR of purified WTAs further reveals peptide polymer interactions as well as the residues responsible for recognition. These findings broaden the classical view of AMP action beyond membrane permeabilization, highlighting WTAs as key molecular targets and paving the way for the rational design of peptide antibiotics with tailored specificity.
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