Structural basis for endotoxin neutralization by the eosinophil cationic protein

FEBS J. 2016 Nov;283(22):4176-4191. doi: 10.1111/febs.13915. Epub 2016 Oct 31.

Abstract

Acute infection by Gram-negative pathogens can induce an exacerbated immune response that leads to lethal septic shock syndrome. Bacterial lipopolysaccharide (LPS) is a major pathogen-associated molecular pattern molecule that can initiate massive and lethal immune system stimulation. Therefore, the development of new and effective LPS-neutralizing agents is a top priority. The eosinophil cationic protein (ECP) is an antimicrobial protein secreted in response to infection, with a remarkable affinity for LPS. In the present study, we demonstrate that ECP is able to neutralize bacterial LPS and inhibit tumor necrosis factor-α production in human macrophages. We also characterized ECP neutralizing activity using progressively truncated LPS mutants, and conclude that the polysaccharide moiety and lipid A portions are required for LPS-mediated neutralization. In addition, we mapped the structural determinants required for the ECP-LPS interaction by nuclear magnetic resonance. Our results show that ECP is able to neutralize LPS and therefore opens a new route for developing novel therapeutic agents based on the ECP structural scaffolding.

Keywords: antimicrobial peptides; endotoxin; eosinophil cationic protein; lipopolysaccharide; structure-function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Cell Line, Tumor
  • Endotoxins / chemistry
  • Endotoxins / metabolism*
  • Endotoxins / pharmacology
  • Eosinophil Cationic Protein / chemistry
  • Eosinophil Cationic Protein / metabolism*
  • Eosinophil Cationic Protein / pharmacology
  • Humans
  • Kinetics
  • Lipopolysaccharides / chemistry
  • Lipopolysaccharides / metabolism*
  • Lipopolysaccharides / pharmacology
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Protein Binding
  • Protein Domains
  • Protein Structure, Secondary
  • Sequence Homology, Amino Acid
  • Spectrometry, Fluorescence
  • Thermodynamics
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Endotoxins
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha
  • Eosinophil Cationic Protein