细菌
肽
生物膜
连接器
纳米纤维
抗生素
微生物学
金黄色葡萄球菌
化学
细胞生物学
生物
纳米技术
生物化学
材料科学
操作系统
计算机科学
遗传学
作者
Tingting Li,Ci Zhu,Liang Chen,Tingfen Deng,Xia Wu,Kang Wen,Xinxin Feng,Dan Yuan,Bing Xu,Junfeng Shi
标识
DOI:10.1021/acsanm.3c00912
摘要
The abuse of antibiotics has led to the emergence of various drug-resistant bacterial strains that threaten human health. Other than a continuous screen for antibiotics, alternative strategies need to be adopted to inhibit bacterial invasion. Herein, we de novo designed a self-assembling peptide that contains a bacteria-binding domain, a linker, and a self-assembly motif. This peptide could specifically bind with a surface protein on Staphylococcus aureus, subsequently self-assemble to form nanofibers, and selectively engulf and trap the bacteria. Thus, these trapped bacteria lack the ability to invade host cells and are unable to form a biofilm. More importantly, the designed peptide is nontoxic to human cells. Such a "trap but not kill" strategy could serve as an alternative to conventional antibiotics and shows great potential for treating bacteria.
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