Two Hits Are Better than One: Membrane-Active and DNA Binding-Related Double-Action Mechanism of NK-18, a Novel Antimicrobial Peptide Derived from Mammalian NK-Lysin

被引:108
作者
Yan, Jiexi [1 ]
Wang, Kairong [1 ]
Dang, Wen [1 ]
Chen, Ru [1 ]
Xie, Junqiu [1 ]
Zhang, Bangzhi [1 ]
Song, Jingjing [1 ]
Wang, Rui [1 ]
机构
[1] Lanzhou Univ, Sch Life Sci, Inst Biochem & Mol Biol, Sch Basic Med Sci,Key Lab Preclin Study New Drugs, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
OUTER-MEMBRANE; POLYBIA-CP; MODE; BACTERIAL; ANTIBIOTICS; RESISTANCE; SEQUENCE; INNATE; MICROORGANISMS; SELECTIVITY;
D O I
10.1128/AAC.01619-12
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The extensive use and misuse of antibiotics in medicine result in the emergence of multidrug-resistant bacteria, creating an urgent need for the development of new chemotherapeutic agents. Nowadays, antimicrobial peptides are widely recognized as a class of promising candidates with activity against multidrug-resistant bacteria. NK-18 is a truncated peptide derived from NK-Lysin, an effector of cytotoxic T cells and natural killer cells. In this study, we studied the antibacterial mechanism of action of NK-18. The results revealed that NK-18 has potent antibacterial activity against Escherichia coli and Staphylococcus aureus. According to our findings, NK-18 is membrane active and its target of action is not only the bacterial membrane but also the DNA in the cytoplasm. The double targets of NK-18 make it difficult for bacteria to generate resistance, which may present a new strategy to defend against multidrug-resistant bacteria and provide a new lead in the design of potent antimicrobial peptides with therapeutic application in the presence of increasing resistance to conventional antibiotics.
引用
收藏
页码:220 / 228
页数:9
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