Alzheimer's disease: correlation of the suppression of beta-amyloid peptide secretion from cultured cells with inhibition of the chymotrypsin-like activity of the proteasome

J Neurochem. 1999 Jul;73(1):195-204. doi: 10.1046/j.1471-4159.1999.0730195.x.

Abstract

Peptide aldehyde inhibitors of the chymotrypsin-like activity of the proteasome (CLIP) such as N-acetyl-Leu-Leu-Nle-H (or ALLN) have been shown previously to inhibit the secretion of beta-amyloid peptide (A beta) from cells. To evaluate more fully the role of the proteasome in this process, we have tested the effects on A beta formation of a much wider range of peptide-based inhibitors of CLIP than published previously. The inhibitors tested included several peptide boronates, some of which proved to be the most potent peptide-based inhibitors of beta-amyloid production reported so far. We found that the ability of the peptide aldehyde and boronate inhibitors to suppress A beta formation from cells correlated extremely well with their potency as CLIP inhibitors. Thus, we conclude that the proteasome may be involved either directly or indirectly in A beta formation.

MeSH terms

  • Aldehydes / pharmacology
  • Alzheimer Disease / metabolism*
  • Amyloid beta-Peptides / analysis
  • Amyloid beta-Peptides / metabolism*
  • Amyloid beta-Protein Precursor / genetics
  • Boronic Acids / pharmacology
  • Cell Line
  • Chymotrypsin / antagonists & inhibitors*
  • Chymotrypsin / metabolism
  • Cysteine Endopeptidases / metabolism*
  • Multienzyme Complexes / metabolism*
  • Peptide Fragments / analysis
  • Peptide Fragments / metabolism
  • Proteasome Endopeptidase Complex
  • Transfection

Substances

  • Aldehydes
  • Amyloid beta-Peptides
  • Amyloid beta-Protein Precursor
  • Boronic Acids
  • Multienzyme Complexes
  • Peptide Fragments
  • Chymotrypsin
  • Cysteine Endopeptidases
  • Proteasome Endopeptidase Complex