Development of novel LL-37 derived antimicrobial peptides with LPS and LTA neutralizing and antimicrobial activities for therapeutic application

Peptides. 2006 Apr;27(4):649-60. doi: 10.1016/j.peptides.2005.09.016. Epub 2005 Nov 7.

Abstract

New peptides for lipopolysaccharide (LPS) and lipoteichoic acid (LTA) neutralization in upper respiratory tract infections were developed and evaluated in terms of efficacy and safety for application in humans. Based on the sequence of the human antimicrobial peptide LL-37 we developed and investigated length variants, substitution analogues and modifications to stabilize the peptides to prevent enzymatic degradation and to improve efficacy. The most promising peptide appears P60.4, a 24 amino acid peptide with similar efficacy as LL-37 in terms of LPS and LTA neutralization and lower pro-inflammatory activity. In addition, the acetylated and amidated version of this peptide shows no toxicity and displays higher or equal antimicrobial activity compared to LL-37.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Anti-Infective Agents / chemical synthesis
  • Anti-Infective Agents / chemistry*
  • Anti-Infective Agents / pharmacology*
  • Anti-Infective Agents / therapeutic use
  • Antimicrobial Cationic Peptides / chemical synthesis
  • Antimicrobial Cationic Peptides / chemistry*
  • Antimicrobial Cationic Peptides / pharmacology*
  • Antimicrobial Cationic Peptides / therapeutic use
  • Cathelicidins
  • Disease Models, Animal
  • Guinea Pigs
  • Lipopolysaccharides / antagonists & inhibitors*
  • Lipopolysaccharides / metabolism
  • Male
  • Microbial Sensitivity Tests
  • Molecular Sequence Data
  • Peptides / chemistry*
  • T-Lymphocytes / drug effects
  • Teichoic Acids / antagonists & inhibitors*
  • Teichoic Acids / metabolism

Substances

  • Anti-Infective Agents
  • Antimicrobial Cationic Peptides
  • Cathelicidins
  • Lipopolysaccharides
  • Peptides
  • Teichoic Acids
  • lipoteichoic acid