4.5 Article

Interaction of the antimicrobial peptide ΔM3 with the Staphylococcus aureus membrane and molecular models

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES
Volume 1863, Issue 2, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.bbamem.2020.183498

Keywords

Staphylococcus aureus; Cationic antimicrobial peptide; Lipid bilayer; Peptide-membrane interactions

Funding

  1. University of Antioquia (CODI) [2015-7669]
  2. COLCIENCIAS [120465843150, RC -611-2014]
  3. Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University
  4. European Regional Development Fund [POIG.02.01.00-12-167/08]

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The study demonstrated the antimicrobial activity of the novel synthetic peptide Delta M3, which interacts mainly with the inner monolayer of erythrocyte membrane rich in anionic lipids. The results suggest that Delta M3 is a non-cytotoxic peptide with antibacterial activity.
Staphylococcus aureus is one of the most pathogenic bacteria; infections with it are associated with significant morbidity and mortality in health care facilities. Antimicrobial peptides are a promising next generation antibiotic with great potential against bacterial infections. In this study, evidence is presented of the biological and biophysical properties of the novel synthetic peptide Delta M3. Its antimicrobial activity against the ATCC 25923 and methicillin-resistant S. aureus strains was evaluated. The results showed that Delta M3 has activity in the same mu M range as vancomycin. Biophysical studies were performed with palmitoyloleoylphosphatidylglycerol and cardiolipin liposomes loaded with calcein and used to follow the lytic activity of the peptide by fluorescence spectroscopy. On the other hand, Delta M3 was induced to interact with molecular models of the erythrocyte membrane buil-up of dimiristoylphosphatidylcholine and dimyristoylphosphatidylethanolamine, representative lipids of the outer and inner monolayers of the human erythrocyte membrane, respectively. The capacity of Delta M3 to interact with the bacteria and erythrocyte model membranes was also evaluated by X-ray diffraction and differential scanning calorimetry. The morphological changes induced by the peptide to human erythrocytes were observed by scanning electron microscopy. Results with these techniques indicated that Delta M3 interacted with the inner monolayer of the erythrocyte membrane, which is rich in anionic lipids. Additionally, the cytotoxic effects of Delta M3 on red blood cells were evaluated by monitoring the hemoglobin release from erythrocytes. The results obtained from these different approaches showed Delta M3 to be a non-cytotoxic peptide with antibacterial activity.

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