TY - JOUR
T1 - Antibacterial lipo-random peptide mixtures exhibit high selectivity and synergistic interactions
AU - Topman-Rakover, Shiri
AU - Malach, Einav
AU - Burdman, Saul
AU - Hayouka, Zvi
N1 - Publisher Copyright:
© The Royal Society of Chemistry 2020.
PY - 2020/10/14
Y1 - 2020/10/14
N2 - Random peptide mixtures (RPMs) have been recently proposed as powerful antimicrobial compounds. These are unique mixtures of peptides synthesized by random combination of a cationic and a hydrophobic amino acid. Here, we introduce a new type of antimicrobial compounds, short lipo-RPMs, which result fromN-palmitoylation of RPMs. We report the characterization of 5-mer lipo-RPMs containingl-phenylalanine andd-lysine, named p-FdK5. p-FdK5 had high antibacterial activity against several bacterial strains and was able to reduce disease severity caused by a plant pathogen. We further synthesized and studied all 32 (25) possible lipopeptides that compose the p-FdK5 mixture. We showed that the antibacterial activity of specific lipopeptides depends on the peptide hydrophobicity and on the location of the hydrophobic amino acids relative to the palmitic acid. Interestingly, synergism assays revealed positive interactions between different sequence-specific lipopeptides in terms of antimicrobial activity.
AB - Random peptide mixtures (RPMs) have been recently proposed as powerful antimicrobial compounds. These are unique mixtures of peptides synthesized by random combination of a cationic and a hydrophobic amino acid. Here, we introduce a new type of antimicrobial compounds, short lipo-RPMs, which result fromN-palmitoylation of RPMs. We report the characterization of 5-mer lipo-RPMs containingl-phenylalanine andd-lysine, named p-FdK5. p-FdK5 had high antibacterial activity against several bacterial strains and was able to reduce disease severity caused by a plant pathogen. We further synthesized and studied all 32 (25) possible lipopeptides that compose the p-FdK5 mixture. We showed that the antibacterial activity of specific lipopeptides depends on the peptide hydrophobicity and on the location of the hydrophobic amino acids relative to the palmitic acid. Interestingly, synergism assays revealed positive interactions between different sequence-specific lipopeptides in terms of antimicrobial activity.
UR - http://www.scopus.com/inward/record.url?scp=85092587616&partnerID=8YFLogxK
U2 - 10.1039/d0cc04493h
DO - 10.1039/d0cc04493h
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 32902531
AN - SCOPUS:85092587616
SN - 1359-7345
VL - 56
SP - 12053
EP - 12056
JO - Chemical Communications
JF - Chemical Communications
IS - 80
ER -