Surface-Induced Peptide Nanofibers for Selective Bacteria Trapping

被引:8
|
作者
Li, Tingting [1 ]
Zhu, Ci [1 ]
Liang, Chen [1 ,2 ]
Deng, Tingfen [1 ]
Feng, Xinxin [3 ]
Yuan, Dan [1 ,4 ]
Shi, Junfeng [1 ,4 ]
Xu, Bing [4 ]
Wu, Xia [2 ]
Wen, Kang [3 ]
机构
[1] Hunan Univ, Sch Biomed Sci, State Key Lab Chemo Biosensingand Chemometr, Changsha 410082, Peoples R China
[2] Shenzhen Int Inst Biomed Res, Shenzhen 518116, Guangdong, Peoples R China
[3] Hunan Univ, Inst Chem Biol & Nanomed, Changsha 410082, Hunan, Peoples R China
[4] Brandeis Univ, Dept Chem, Waltham, MA 02453 USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
self-assembly; nanofibers; peptide hydrogel; human cytokeratin 10; selective bacterial trapping; SELF-ASSEMBLED PEPTIDE; ALPHA-DEFENSIN; 6; SMALL MOLECULES; AMINO-ACIDS;
D O I
10.1021/acsanm.3c00912
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
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.
引用
收藏
页码:7785 / 7793
页数:9
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