Novel short AMP: design and activity study.

Abstract

In a previous study, we reported that truncation of HP (2-20) (derived from the N-terminal region of Helicobacter pylori Ribosomal Protein L1 (RPL1)) at the N- (residues 2-3) and C-terminal (residues 17-20) truncated fragments to give HP (4-16) induces increased antibiotic activity against several bacterial strains without hemolysis. In this study, to develop novel short antibiotic peptides useful as therapeutic drugs, an analogue was designed to possess increased hydrophobicity by Trp substitution in position 2 region of HP (4-16). Synthetic HP (4-16)-W showed an enhanced antimicrobial and antitumor activity. The antimicrobial activity of this peptide and others was measured by their growth inhibitory effect upon S. aureus, B. subtilis, S. epidermidis, E. coli, S. typimurium, P. aeruginosa, C. albicans, T. beigelii and S. cerevisiae. None of the peptides exhibited hemolytic activity against human erythrocyte cells except melittin as a positive control. Its antibiotic activity suggests that HP (4-16)-W is an excellent candidate as a lead compound for the development of novel antibiotic agents.

• Authors: Yoonkyung Park, Kyung-Soo Hahm
• Journal: Protein and peptide letters (Protein Pept Lett) Vol. 19 Issue 6 Pg. 652-6 (Jun 01 2012) ISSN: 1875-5305 [Electronic] Netherlands
• PMID: 21838696 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Anti-Bacterial Agents
• Antifungal Agents
• Antimicrobial Cationic Peptides
• Antineoplastic Agents
• Peptide Fragments
• Ribosomal Proteins
• ribosomal protein L1
• Melitten
• Tryptophan

Topics

• Amino Acid Sequence
• Anti-Bacterial Agents (chemistry, metabolism, pharmacology)
• Antifungal Agents (chemistry, metabolism, pharmacology)
• Antimicrobial Cationic Peptides (chemistry, genetics, metabolism, pharmacology)
• Antineoplastic Agents (chemistry, metabolism, pharmacology)
• Bacteria (drug effects)
• Cell Line, Tumor
• Cell Survival (drug effects)
• Drug Discovery
• Erythrocytes
• Helicobacter pylori (genetics, metabolism)
• Hemolysis (drug effects)
• Humans
• Hydrophobic and Hydrophilic Interactions
• Melitten (pharmacology)
• Molecular Sequence Data
• Peptide Fragments (chemistry, genetics, metabolism, pharmacology)
• Protein Engineering (methods)
• Ribosomal Proteins (chemistry, genetics, metabolism, pharmacology)
• Tryptophan (genetics, metabolism)
• Yeasts (drug effects)