Characterization of immunoaffinity purified peptidoglycan-associated lipoprotein of Actinobacillus actinomycetemcomitans

J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Feb 2;831(1-2):116-25. doi: 10.1016/j.jchromb.2005.11.052. Epub 2005 Dec 27.

Abstract

Peptidoglycan-associated lipoprotein (PAL) is a highly conserved structural outer membrane protein among Gram-negative bacteria. In some species, it is proinflammatory and released extracellularly. We purified a newly identified PAL (AaPAL) of a periodontal pathogen Actinobacillus actinomycetemcomitans by using AaPAL antipeptide antibodies coupled to immunoaffinity chromatography column. No protein impurities originating in A. actinomycetemcomitans were found in the final product. Sera from patients infected by A. actinomycetemcomitans recognized the purified AaPAL. The present purification method seems to be suitable for isolation of AaPAL and probably PALs of other bacterial species, and applicable in studies investigating proinflammatory mechanisms of A. actinomycetemcomitans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aggregatibacter actinomycetemcomitans / chemistry*
  • Aggregatibacter actinomycetemcomitans / immunology
  • Bacterial Outer Membrane Proteins / isolation & purification*
  • Chromatography, Affinity / methods*
  • Humans
  • Immunoblotting
  • Lipoproteins / isolation & purification*
  • Peptidoglycan / isolation & purification*

Substances

  • Bacterial Outer Membrane Proteins
  • Lipoproteins
  • Peptidoglycan