磷脂酰丝氨酸
两亲性
磷脂
化学
抗菌剂
抗菌肽
生物化学
膜
生物物理学
大肠杆菌
磷脂酰胆碱
肽
细菌
抗菌活性
合成膜
生物相容性
磷脂酰乙醇胺
蛋白质工程
选择性
组合化学
作者
Yueling Yuan,Zeyu Yao,Bingchuan Huang,Yangbin Liang,Zhouming Zhang,Meishan Ye,Chanjuan Su,Houbing Zhang,Menghua Xiong,Liping Zhao,Fuxiang Wang,Huosheng Zhou,Rui Yang,Xinshuang Zhang,Yan Bao
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2026-03-19
卷期号:27 (4): 2536-2542
标识
DOI:10.1021/acs.biomac.5c02223
摘要
The differences in the phospholipid profile between bacterial and mammalian membranes present a promising direction for designing antimicrobial peptides (AMPs). A key challenge, however, is engineering AMPs with a high affinity for bacterial anionic phospholipid (phosphatidylglycerol, PG) while minimizing off-target interactions with mammalian phosphatidylserine (PS). Herein, we report a multiarmed radially amphiphilic AMP (maRAP) design that enhances PG recognition, exhibiting potent antibacterial activity and exceptional antibacterial selectivity. Compared to the single-arm RAP (1aRAP), maRAPs exhibited superior affinity for PG, yet they exhibited negligible binding to PS. They also demonstrated significantly enhanced bactericidal efficacy and selectivity over 1aRAP in complex physiological environments. In the murine bladder-infection model, maRAPs more effectively reduced the bacterial load and attenuated infection-induced tissue damage, as demonstrated by an intact urothelial lining and minimal lamina propria edema at the infection site. This work presents the multiarm strategy as an effective approach for advanced AMP development.
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