Antimicrobial activity of the indolicidin-derived novel synthetic peptide In-58.
Alexey S VasilchenkoA V VasilchenkoT M PashkovaM P SmirnovaN I KolodkinI V ManukhovG B ZavilgelskyE A SizovaO L KartashovaA S SimbirtsevE A RogozhinG K DuskaevM V SychevaPublished in: Journal of peptide science : an official publication of the European Peptide Society (2018)
Natural peptides with antimicrobial activity are extremely diverse, and peptide synthesis technologies make it possible to significantly improve their properties for specific tasks. Here, we investigate the biological properties of the natural peptide indolicidin and the indolicidin-derived novel synthetic peptide In-58. In-58 was generated by replacing all tryptophan residues on phenylalanine in D-configuration; the α-amino group in the main chain also was modified by unsaturated fatty acid. Compared with indolicidin, In-58 is more bactericidal, more resistant to proteinase K, and less toxic to mammalian cells. Using molecular physics approaches, we characterized the action of In-58 on bacterial cells at the cellular level. Also, we have found that studied peptides damage bacterial membranes. Using the Escherichia coli luminescent biosensor strain MG1655 (pcolD'::lux), we investigated the action of indolicidin and In-58 at the subcellular level. At subinhibitory concentrations, indolicidin and In-58 induced an SOS response. Our data suggest that indolicidin damages the DNA, but bacterial membrane perturbation is its principal mode of action. Copyright © 2017 European Peptide Society and John Wiley & Sons, Ltd.
Keyphrases
- escherichia coli
- fatty acid
- induced apoptosis
- sensitive detection
- single molecule
- oxidative stress
- gold nanoparticles
- high resolution
- cell death
- cystic fibrosis
- circulating tumor
- signaling pathway
- amino acid
- multidrug resistant
- pseudomonas aeruginosa
- electronic health record
- diabetic rats
- artificial intelligence
- pi k akt
- stress induced