'Click peptide': a novel 'O-acyl isopeptide method' for peptide synthesis and chemical biology-oriented synthesis of amyloid beta peptide analogues

J Pept Sci. 2006 Dec;12(12):823-8. doi: 10.1002/psc.817.

Abstract

After over a decade of studies on aspartic protease inhibitors and water-soluble prodrugs, we have been developing a novel method, since 2003, called 'O-acyl isopeptide method', for the synthesis of peptides containing difficult sequences. With our recent discoveries of 'O-acyl isodipeptide unit' and the 'racemization-free segment condensation method', this method has further evolved as a general synthetic method for peptides. Moreover, 'Click Peptide', which could be a powerful tool for identifying the pathological functions of amyloid beta peptides in Alzheimer's disease, represents a valuable use of the isopeptide method in Chemical Biology-oriented research.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acylation
  • Amino Acid Sequence
  • Amyloid beta-Peptides / chemical synthesis*
  • Amyloid beta-Peptides / chemistry
  • Drug Stability
  • Models, Chemical
  • Molecular Sequence Data
  • Molecular Structure
  • Peptide Fragments / chemical synthesis*
  • Peptide Fragments / chemistry
  • Prodrugs / chemical synthesis
  • Prodrugs / chemistry

Substances

  • Amyloid beta-Peptides
  • Peptide Fragments
  • Prodrugs