Synthetic peptide-based activators of the proteasome

Sherwin Wilk, Wei Er Chen

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

The development of small molecule peptide-based activators of the 20S proteasome or multicatalytic proteinase complex was initiated. The enhancement of antigen presentation by transfection of the protein activator PA28α into a mouse fibroblast cell line [10] supports the potential use of small molecule activators in stimulating the immune response. Four classes of peptide-based activators were synthesized, i.e. peptidyl alcohols, esters, p-nitroanilides and nitriles. These compounds markedly and reversibly stimulated the hydrolysis of suc-LLVY-MCA, Z-LLE-NA and Z-GPALG-p-aminobenzoate as well as hydrolysis of the decapeptide angiotensin 1. Stimulation was due to a decrease in the K(m) and increase in the V(max) of the substrate. In general, the EC50 for activation ranged from 50-150 mM and maximal stimulation varied from 3 to 15 fold depending on the activity measured. Z-IE(O-tBu)AL-p-nitroanilide, a proteasome substrate, markedly stimulated the hydrolysis of Z-GPALG-pAB by binding to a saturable high affinity site distinct from its binding site as substrate. Since all effective activators contain hydrophobic groups in positions P1-P5, low aqueous solubility is a limitation of these compounds. Competition experiments suggest that these activators bind to the same site as PA28.

Original languageEnglish
Pages (from-to)119-124
Number of pages6
JournalMolecular Biology Reports
Volume24
Issue number1-2
DOIs
StatePublished - 1997

Keywords

  • Antigen presentation
  • MHC-1
  • PA28
  • Peptide-based activators
  • Proteasome activator

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