A method for N-terminal de novo sequence analysis of proteins by matrix-assisted laser desorption/ionization mass spectrometry

Anal Biochem. 2008 Sep 15;380(2):291-6. doi: 10.1016/j.ab.2008.05.053. Epub 2008 Jun 7.

Abstract

A novel method for isolation and de novo sequencing of N-terminal peptides from proteins is described. The method presented here combines selective chemical tagging using succinimidyloxycarbonylmethyl tris(2,4,6-trimethoxyphenyl)phosphonium bromide (TMPP-Ac-OSu) at the N(alpha)-amino group of peptides after digestion by metalloendopeptidase (from Grifola frondosa) and selective capture procedures using p-phenylenediisothiocyanate resin, by which the N-terminal peptide can be isolated, whether or not it is N-terminally blocked. The isolated N-terminal peptide modified N-terminally with TMPP-Ac-OSu reagent produces a simple fragmentation pattern under tandem mass spectrometric analysis to significantly facilitate sequencing.

MeSH terms

  • Animals
  • Carbonic Anhydrase II / analysis
  • Carbonic Anhydrase II / chemistry
  • Hemoglobins / analysis
  • Hemoglobins / chemistry
  • Humans
  • Lactalbumin / analysis
  • Lactalbumin / chemistry
  • Peptide Fragments / analysis*
  • Peptide Fragments / isolation & purification
  • Proteins / analysis*
  • Proteins / chemistry
  • Sequence Analysis, Protein / methods*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization / methods*

Substances

  • Hemoglobins
  • Peptide Fragments
  • Proteins
  • Lactalbumin
  • Carbonic Anhydrase II