EcDBS1R6: A novel cationic antimicrobial peptide derived from a signal peptide sequence

Biochim Biophys Acta Gen Subj. 2020 Sep;1864(9):129633. doi: 10.1016/j.bbagen.2020.129633. Epub 2020 May 13.

Abstract

Background: Bacterial infections represent a major worldwide health problem the antimicrobial peptides (AMPs) have been considered as potential alternative agents for treating these infections. Here we demonstrated the antimicrobial activity of EcDBS1R6, a peptide derived from a signal peptide sequence of Escherichia coli that we previously turned into an AMP by making changes through the Joker algorithm.

Methods: Antimicrobial activity was measured by broth microdilution method. Membrane integrity was measured using fluorescent probes and through scanning electron microscopy imaging. A sliding window of truncated peptides was used to determine the EcDBS1R6 active core. Molecular dynamics in TFE/water environment was used to assess the EcDBS1R6 structure.

Results: Signal peptides are known to naturally interact with membranes; however, the modifications introduced by Joker transformed this peptide into a membrane-active agent capable of killing bacteria. The C-terminus was unable to fold into an α-helix whereas its fragments showed poor or no antimicrobial activity, suggesting that the EcDBS1R6 antibacterial core was located at the helical N-terminus, corresponding to the signal peptide portion of the parent peptide.

Conclusion: The strategy of transforming signal peptides into AMPs appears to be promising and could be used to produce novel antimicrobial agents.

General significance: The process of transforming an inactive signal peptide into an antimicrobial peptide could open a new venue for creating new AMPs derived from signal peptides.

Keywords: Joker algorithm; Mechanism of action; Membrane damage; Rational design; Sliding window.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Antimicrobial Cationic Peptides / chemistry*
  • Antimicrobial Cationic Peptides / pharmacology*
  • Escherichia coli / chemistry*
  • Gram-Negative Bacteria / drug effects
  • Microbial Sensitivity Tests
  • Molecular Dynamics Simulation
  • Protein Conformation
  • Protein Sorting Signals*

Substances

  • Antimicrobial Cationic Peptides
  • Protein Sorting Signals