TY - JOUR
T1 - Human microbiome derived synthetic antimicrobial peptides with activity against Gram-negative, Gram-positive, and antibiotic resistant bacteria
AU - Mousa, Walaa K.
AU - Shaikh, Ashif Y.
AU - Ghemrawi, Rose
AU - Aldulaimi, Mohammed
AU - Al Ali, Aya
AU - Sammani, Nour
AU - Khair, Mostafa
AU - Helal, Mohamed I.
AU - Al-Marzooq, Farah
AU - Oueis, Emilia
N1 - Publisher Copyright:
© 2024 RSC.
PY - 2024
Y1 - 2024
N2 - The prevalence of antibacterial resistance has become one of the major health threats of modern times, requiring the development of novel antibacterials. Antimicrobial peptides are a promising source of antibiotic candidates, mostly requiring further optimization to enhance druggability. In this study, a series of new antimicrobial peptides derived from lactomodulin, a human microbiome natural peptide, was designed, synthesized, and biologically evaluated. Within the most active region of the parent peptide, linear peptide LM6 with the sequence LSKISGGIGPLVIPV-NH2 and its cyclic derivatives LM13a and LM13b showed strong antibacterial activity against Gram-positive bacteria, including resistant strains, and Gram-negative bacteria. The peptides were found to have a rapid onset of bactericidal activity and transmission electron microscopy clearly shows the disintegration of the cell membrane, suggesting a membrane-targeting mode of action.
AB - The prevalence of antibacterial resistance has become one of the major health threats of modern times, requiring the development of novel antibacterials. Antimicrobial peptides are a promising source of antibiotic candidates, mostly requiring further optimization to enhance druggability. In this study, a series of new antimicrobial peptides derived from lactomodulin, a human microbiome natural peptide, was designed, synthesized, and biologically evaluated. Within the most active region of the parent peptide, linear peptide LM6 with the sequence LSKISGGIGPLVIPV-NH2 and its cyclic derivatives LM13a and LM13b showed strong antibacterial activity against Gram-positive bacteria, including resistant strains, and Gram-negative bacteria. The peptides were found to have a rapid onset of bactericidal activity and transmission electron microscopy clearly shows the disintegration of the cell membrane, suggesting a membrane-targeting mode of action.
UR - http://www.scopus.com/inward/record.url?scp=85207784994&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85207784994&partnerID=8YFLogxK
U2 - 10.1039/d4md00383g
DO - 10.1039/d4md00383g
M3 - Article
AN - SCOPUS:85207784994
SN - 2040-2503
JO - RSC Medicinal Chemistry
JF - RSC Medicinal Chemistry
ER -