Lipopolysaccharide (LPS)-binding proteins BPI and LBP form different types of complexes with LPS

J Biol Chem. 1997 Jul 25;272(30):18682-5. doi: 10.1074/jbc.272.30.18682.

Abstract

Lipopolysaccharide (LPS)-binding protein (LBP) and bactericidal/permeability-increasing protein (BPI) are closely related LPS-binding proteins whose binding to LPS has markedly different functional consequences. To gain better insight into the possible basis of these functional differences, the physical properties of LBP-LPS and BPI-LPS complexes have been compared in this study by sedimentation, light scattering, and fluorescence analyses. These studies reveal dramatic differences in the physical properties of LPS complexed to LBP versus BPI. They suggest that of the two proteins, only LBP can disperse LPS aggegates. However, BPI can enhance both the sedimentation velocity and apparent size of LPS aggregates while inhibiting LPS-LBP binding even at very low (1:40 to 1:20) BPI:LPS molar ratios.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acute-Phase Proteins*
  • Antimicrobial Cationic Peptides
  • Blood Proteins / metabolism
  • Carrier Proteins / metabolism
  • Centrifugation, Density Gradient
  • Fluorescein-5-isothiocyanate / metabolism
  • Humans
  • Light
  • Lipopolysaccharides / metabolism*
  • Macromolecular Substances
  • Membrane Glycoproteins*
  • Membrane Proteins*
  • Protein Binding
  • Scattering, Radiation
  • Spectrometry, Fluorescence

Substances

  • Acute-Phase Proteins
  • Antimicrobial Cationic Peptides
  • Blood Proteins
  • Carrier Proteins
  • Lipopolysaccharides
  • Macromolecular Substances
  • Membrane Glycoproteins
  • Membrane Proteins
  • bactericidal permeability increasing protein
  • lipopolysaccharide-binding protein
  • Fluorescein-5-isothiocyanate