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Tuning the antimicrobial pharmacophore to enable discovery of short lipopeptides with multiple modes of action

Journal 2014 · IF 3.432 · 发表于 2014 年 6 月 4 日
作者: Yuxin Fang,Wenjing Zhong,Yue Wang,Tianrong Xun,Dongguo Lin,Wenjun Liu,Jingyu Wang,Lin Lv,Shuwen Liu,Jian He
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摘要

Tryptophan and arginine rich antimicrobial peptides (AMPs) possess high potencies against both gram positive and gram negative bacteria , while lipopeptides represent another family of promising antimicrobial agents to combat invading pathogens. In the present study, we have synthesized a series of very short arginine, lysine and tryptophan containing lipopeptides and evaluated their antimicrobial activities against a panel of pathogenic microorganisms including Staphylococcus aureus , Escherichia coli , and Candida albicans . The results showed that most of these peptides were effective against tested strains with MIC values ranging from 3.9 to 62.5 μg/mL. In addition to the small size, potent bactericidal activity , low to moderate hemolytic toxicity and membrane disruption ability, several peptides such as C10-RIKWWK and C10-RKWWK apparently retarded the migration of DNA on agarose gel in the DNA-binding assay, which implied the multiple modes of action in their bacteria-killing mechanism. These peptides revealed a promising therapeutic potential to develop as new antimicrobial agents.

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