抗菌肽
化学
抗菌剂
微生物学
抗生素
抗生素耐药性
体内
细菌
细菌细胞结构
生物物理学
生物化学
生物
遗传学
生物技术
作者
Minghui Zhang,Jianhong Ouyang,Linglin Fu,Cheng Xu,Yuke Ge,Shuqing Sun,Xiangyuan Li,Shian Lai,Hengte Ke,Bing Yuan,Kai Yang,Haining Yu,Lianghui Gao,Yipeng Wang
标识
DOI:10.1021/acs.jmedchem.2c01238
摘要
Rapid antimicrobial action is an important advantage of antimicrobial peptides (AMPs) over antibiotics, which is also a reason for AMPs being less likely to induce bacterial resistance. However, the structural parameters and underlying mechanisms affecting the bacterial killing rate of AMPs remain unknown. In this study, we performed a structure–activity relationship (SAR) study using As-CATH4 and 5 as templates. We revealed that hydrophobicity, rather than other characteristics, is the critical structural parameter determining the bacterial killing rate of α-helical AMPs. With the hydrophobicity increase, the action rates of AMPs including bacterial binding, lipopolysaccharides neutralization, and outer and inner membrane permeabilization increased. Additionally, the higher hydrophobic AMPs with enhanced bacterial killing rates possess better in vivo therapeutic potency and a lower propensity to induce bacterial resistance. These findings revealed the importance of the bacterial killing rate for AMPs and are of great significance to the design and optimization of AMP-related drugs.
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