| Literature DB >> 32083767 |
Min Zhou1, Yuxin Qian1, Jiayang Xie1, Wenjing Zhang1, Weinan Jiang1, Ximian Xiao1, Sheng Chen1, Chengzhi Dai1, Zihao Cong1, Zhemin Ji1, Ning Shao1, Longqiang Liu1, Yuequn Wu1, Runhui Liu1.
Abstract
Peptides have important biological functions. However, their susceptibility to proteolysis limits their applications. We demonstrated here for the first time, that poly(2-oxazoline) (POX) can work as a functional mimic of peptides. POX-based glycine pseudopeptides, a host defense peptide mimic, had potent activities against methicillin-resistant S. aureus, which causes formidable infections. The POX mimic showed potent activity against persisters that are highly resistant to antibiotics. S. aureus did not develop resistance to POX owning to the reactive oxygen species related antimicrobial mechanism. POX-treated S. aureus is sensitive to common antibiotics, demonstrating no observable antimicrobial pressure or cross-resistance in using antimicrobial POX. This study highlights POX as a new type of functional mimic of peptides and opens new avenues in designing and exploring peptide mimetics for biological functions and applications.Entities:
Keywords: antibiotics; antimicrobials; drug design; peptides; polymers
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Year: 2020 PMID: 32083767 DOI: 10.1002/anie.202000505
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336