Michael addition-type 4-hydroxy-2-nonenal adducts in modified low-density lipoproteins: markers for atherosclerosis

Biochemistry. 1994 Oct 18;33(41):12487-94. doi: 10.1021/bi00207a016.

Abstract

It has been proposed that plasma low-density lipoprotein (LDL) undergoes oxidative modification before it can give rise to foam cells in atherosclerosis. Oxidation of LDL generates a variety of reactive aldehyde products including 4-hydroxy-2-nonenal (HNE), which may covalently attach to the LDL apolipoproteins. We here present direct evidence that HNE derivatization of LDL forms Michael addition-type adducts of HNE with histidine and lysine residues of apolipoprotein B-100 (apoB) and also demonstrate the utility of an antibody specific to the HNE adducts generated in the LDL treated with HNE or oxidatively modified by Cu2+ or cultured endothelial cells. HNE adducts present in the LDL that had been treated with HNE were attested to be Michael addition-type adducts on the basis of the fact that incubation of LDL with 1 mM HNE (2 h, 37 degrees C) resulted primarily in the formation of Michael addition-type HNE-histidine (39.9 mol/mol of LDL) and HNE-lysine (19.3 mol/mol of LDL) adducts. An enzyme-linked immunosorbent assay (ELISA) and an SDS-polyacrylamide gel electrophoresis (SDS-PAGE)/immunoblot analysis of HNE-modified LDL demonstrated that these HNE adducts were detectable with the HNE-specific antibody affinity-purified with the Michael adduct (HNE-histidine) as a ligand. The following lines of evidence indicated the presence of Michael addition-type HNE adducts in the oxidatively modified LDL in vitro: (i) Amino acid analysis of LDL that had been treated with Cu2+ (24 h, 37 degrees C) demonstrated the presence of a Michael addition-type HNE-histidine adduct (7-9 mol/mol of LDL).(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH terms

  • Aldehydes / immunology
  • Aldehydes / metabolism*
  • Aldehydes / pharmacology
  • Animals
  • Antibodies / metabolism
  • Aorta
  • Apolipoprotein B-100
  • Apolipoproteins B / metabolism
  • Arteriosclerosis / metabolism*
  • Binding, Competitive
  • Cattle
  • Cells, Cultured
  • Copper / pharmacology
  • Electrophoresis, Polyacrylamide Gel
  • Endothelium, Vascular / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Histidine / metabolism
  • Humans
  • Immunoblotting
  • Lipoproteins, LDL / metabolism*
  • Lysine / metabolism
  • Malondialdehyde / metabolism
  • Oxidation-Reduction
  • Thiobarbituric Acid Reactive Substances / metabolism

Substances

  • Aldehydes
  • Antibodies
  • Apolipoprotein B-100
  • Apolipoproteins B
  • Lipoproteins, LDL
  • Thiobarbituric Acid Reactive Substances
  • Histidine
  • Malondialdehyde
  • Copper
  • 4-hydroxy-2-nonenal
  • Lysine