抗菌剂
抗菌肽
抗生素
细菌
微生物学
肽
万古霉素
化学
抗生素耐药性
生物
金黄色葡萄球菌
生物化学
遗传学
作者
Chih‐Lung Wu,Kuang-Li Peng,Bak‐Sau Yip,Ya‐Han Chih,Jya‐Wei Cheng
标识
DOI:10.3389/fmicb.2021.747760
摘要
The global spread of antibiotic-resistant infections has meant that there is an urgent need to develop new antimicrobial alternatives. In this study, we developed a strategy to boost and/or synergize the activity of conventional antibiotics by combination with antimicrobial peptides tagged with the bulky non-natural amino acid β-naphthylalanine (Nal) to their N- or C-terminus. A checkerboard method was used to evaluate synergistic effects of the parent peptide and the Nal-tagged peptides. Moreover, boron-dipyrro-methene labeled vancomycin was used to characterize the synergistic mechanism of action between the peptides and vancomycin on the bacterial strains. These Nal-tagged antimicrobial peptides also reduced the antibiotic-induced release of lipopolysaccharide from Gram-negative bacteria by more than 99.95%. Our results demonstrate that Nal-tagged peptides could help in developing antimicrobial peptides that not only have enhanced antibacterial activities but also increase the synergistic effects with conventional antibiotics against antibiotic-resistant bacteria.
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