Chemical pathways of peptide degradation. II. Kinetics of deamidation of an asparaginyl residue in a model hexapeptide

Pharm Res. 1990 Jul;7(7):703-11. doi: 10.1023/a:1015807303766.

Abstract

Deamidation of Asn residues is a major chemical pathway of degradation of peptides and proteins. To understand better the external factors that influence deamidation, we studied the degradation of the hexapeptide Val-Tyr-Pro-Asn-Gly-Ala, a fragment of adrenocorticotropic hormone, by HPLC. The deamidation of this model peptide showed marked dependence on pH, temperature, and buffer composition. In the pH range 5 to 12, the peptide deamidated exclusively via a cyclic imide intermediate with the formation of both the Asp- and the isoAsp-hexapeptides. Buffer catalysis was also observed in the pH range of 7 to 11. However, at acidic pH's, the pathway of deamidation involved direct hydrolysis of the amide side chain of Asn residue to produce only the Asp-hexapeptide.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / analysis
  • Amino Acid Sequence
  • Asparagine / analysis*
  • Buffers
  • Chromatography, High Pressure Liquid
  • Hydrogen-Ion Concentration
  • Hydrolysis
  • Kinetics
  • Models, Chemical
  • Molecular Sequence Data
  • Oligopeptides / analysis*
  • Oligopeptides / pharmacokinetics
  • Peptide Fragments / analysis*
  • Peptide Fragments / pharmacokinetics
  • Temperature

Substances

  • Amides
  • Buffers
  • Oligopeptides
  • Peptide Fragments
  • valyl-tyrosyl-prolyl-asparaginyl-glycyl-alanine
  • Asparagine