Design of selective substrates of proteinase 3 using combinatorial chemistry methods

Anal Biochem. 2008 Jul 15;378(2):208-15. doi: 10.1016/j.ab.2008.04.003. Epub 2008 Apr 7.

Abstract

In this study, chemical synthesis of the selective chromogenic/fluorogenic substrates for proteinase 3 is described. The substrates' sequence was obtained using combinatorial chemistry methods. Deconvolution of the tripeptide library against proteinase 3 with general formula ABZ-X3-X2-X1-ANB-NH2 yielded the active sequence. Selected peptide was further modified on its C terminus to investigate the impact of chromophore moiety modification on enzyme-substrate interaction. To determine specificity, activity of selected substrates was characterized against proteinase 3 and neutrophil elastase. Finally, the peptide ABZ-Tyr-Tyr-Abu-ANB-NH2 displayed the highest value of specificity constant (k(cat)/K(M)=189 x 10(3) M(-1) s(-1)) for proteinase 3. To the best of our knowledge, this is the first short peptide that undergoes selective proteolysis by proteinase 3 and displays no significant hydrolysis in the presence of human neutrophil elastase and cathepsin G.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Combinatorial Chemistry Techniques / methods*
  • Humans
  • Hydrolysis
  • Leukocyte Elastase / metabolism
  • Mass Spectrometry
  • Myeloblastin / chemistry
  • Myeloblastin / metabolism*
  • Peptides / chemistry
  • Protein Processing, Post-Translational
  • Substrate Specificity
  • Titrimetry

Substances

  • Peptides
  • Leukocyte Elastase
  • Myeloblastin