Study of Novel Peptides for Antimicrobial Protection in Solution and on Cotton Fabric.
Petar T TodorovStela GeorgievaDesislava StanevaPetia PenevaPeter P GrozdanovIvanka Nikolova NikolovaEvgenia Vasileva-TonkovaIvo GrabchevPublished in: Molecules (Basel, Switzerland) (2022)
Some new N- and C-modified biomolecular peptide analogues of both VV-hemorphin-5 and VV-hemorphin-7 with varied amino acids (Cys, Glu, His), 1-adamantanecarboxylic acid, and niacin (nicotinic acid) were synthesized by solid-phase peptide synthesis-Fmoc (9-fluorenylmethoxy-carbonyl) chemistry and were characterized in water solutions with different pH using spectroscopic and electrochemical techniques. Basic physicochemical properties related to the elucidation of the peptide structure at physiological pH have been also studied. The results showed that the interaction of peptide compounds with light and electricity preserves the structural and conformational integrity of the compounds in the solutions. Moreover, textile cotton fibers were modified with the new compounds and the binding of the peptides to the surface of the material was proved by FTIR and SEM analysis. Washing the material with an alkaline soap solution did not show a violation of the modified structure of the cotton. Antiviral activity against the human respiratory syncytial virus (HRSV-S2) and human adenovirus serotype 5 (HAdV-5), the antimicrobial activity against B. cereus and P. aeruginosa used as model bacterial strains and cytotoxic effect of the peptide derivatives and modified cotton textile material has been evaluated. Antimicrobial tests showed promising activity of the newly synthesized compounds against the used Gram-positive and Gram-negative bacteria. The compounds C-V, H-V, AC-V, and AH-V were found slightly more active than NH7C and NCH7. The activity has been retained after the deposition of the compounds on cotton fibers.
Keyphrases
- endothelial cells
- amino acid
- respiratory syncytial virus
- staphylococcus aureus
- wastewater treatment
- gold nanoparticles
- molecular dynamics
- escherichia coli
- gram negative
- single molecule
- molecular dynamics simulations
- mass spectrometry
- multidrug resistant
- molecularly imprinted
- room temperature
- binding protein
- label free
- anaerobic digestion