Interaction with lipopolysaccharide is key to efficacy of tryptophan- and arginine-rich α-melanocyte-stimulating hormone analogs against Gram-negative bacteria.
Kanchan TiwariPriya PatelAftab H MondalKasturi MukhopadhyayPublished in: Future microbiology (2023)
Aim: In order to search for novel antibacterial therapeutics against Gram-negative bacteria, the antibacterial efficacies and mechanism of action of tryptophan- and arginine-rich α-melanocyte-stimulating hormone analogs were investigated. Materials & methods: We performed a killing assay to determine their efficacy; fluorescence, microscopic studies were used to understand their mechanism and peptide-lipopolysaccharide interaction. A checkerboard assay was used to find the effective combination of peptide and antibiotics. Results: Ana-peptides displayed good killing activity against Escherichia coli , Klebsiella pneumoniae and Pseudomonas aeruginosa . Their strong interaction with lipopolysaccharide damaged the bacterial membranes and led to their subsequent death. Ana-5, the highest cationic and hydrophobic analog, emerged as the most potent peptide, showing synergistic action with rifampicin and erythromycin. Conclusion: Ana-5 can be presented as an important therapeutic candidate against bacterial infections.
Keyphrases
- klebsiella pneumoniae
- escherichia coli
- inflammatory response
- toll like receptor
- pseudomonas aeruginosa
- lps induced
- nitric oxide
- multidrug resistant
- high throughput
- molecular docking
- mycobacterium tuberculosis
- cystic fibrosis
- amino acid
- anti inflammatory
- silver nanoparticles
- biofilm formation
- single molecule
- staphylococcus aureus
- case control
- energy transfer
- atomic force microscopy
- quantum dots