Development of radioimmunoassays for free tetra-L-aspartyl-L-lysine trypsinogen activation peptides (TAP)

J Immunol Methods. 1988 Jul 22;111(2):195-203. doi: 10.1016/0022-1759(88)90127-5.


Tetra-L-aspartyl-L-lysine (D4K) containing trypsinogen activation peptides were synthesised on solid-phase supports. Synthetic D4K peptides were N-terminally haptenised and used to generate specific C-terminally directed anti-D4K antibodies. Affinity purification of antisera using Sepharose-immobilised synthetic D4K segregated two highly purified populations of anti-D4K antibodies, one eluting with EDTA recognising the calcium chelate and the other eluting with propionic acid recognising an alternative epitope on the anionic oligopeptide. Both specific anti-D4K antibodies were C-terminally directed and did not bind trypsinogen. Specific antisera and calcium-independent antibodies were used to develop and characterise solution and solid-phase immunoassays specific for free trypsinogen activation peptides (TAP assay), with a detection limit of 10(-11) M and between assay CV of 10.7% for the solution-phase system. The release of D4K peptides by enteropeptidase activation of trypsinogen and dog pancreatic secretion is demonstrated. TAP assays specifically indicate trypsinogen activation and may contribute to the recognition and understanding of disease states such as pancreatitis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Enzyme Activation
  • Molecular Sequence Data
  • Oligopeptides / analysis*
  • Oligopeptides / chemical synthesis
  • Oligopeptides / immunology
  • Peptide Fragments / analysis*
  • Peptide Fragments / immunology
  • Radioimmunoassay
  • Structure-Activity Relationship
  • Trypsinogen / analysis
  • Trypsinogen / immunology*


  • Oligopeptides
  • Peptide Fragments
  • Trypsinogen