类胡萝卜素
抗菌剂
抗菌肽
肽
化学
抗菌活性
微生物学
生物化学
生物
细菌
遗传学
作者
Chenxi Li,Ying Cai,Lin Luo,Gengzhou Tian,Xingyu Wang,Yan An,Liunan Wang,Sijing Wu,Zhongxiang Wu,Tianyu Zhang,Wenlin Chen,Zhiye Zhang
出处
期刊:iScience
[Cell Press]
日期:2024-06-28
卷期号:27 (7): 110404-110404
被引量:3
标识
DOI:10.1016/j.isci.2024.110404
摘要
Cathelicidins, a major class of antimicrobial peptides (AMPs), hold considerable potential for antimicrobial drug development. In the present study, we identified a novel cathelicidin AMP (TC-33) derived from the Chinese tree shrew. Despite TC-33 demonstrating weak antimicrobial activity, the novel peptide TC-14, developed based on its active region, exhibited a 432-fold increase in antimicrobial activity over the parent peptide. Structural analysis revealed that TC-14 adopted an amphipathic α-helical conformation. The bactericidal mechanism of TC-14 involved targeting and disrupting the bacterial membrane, leading to rapid membrane permeabilization and rupture. Furthermore, TC-14 exhibited a high-safety profile, as evidenced by the absence of cytotoxic and hemolytic activities, as well as high biocompatibility and safety in vivo. Of note, its potent antimicrobial activity provided significant protection in a murine model of skin infection. Overall, this study presents TC-14 as a promising drug candidate for antimicrobial drug development.
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