Charge state specific facile gas-phase cleavage of Asp 75-Met 76 peptide bond in the alpha-chain of human apohemoglobin probed by electrospray ionization mass spectrometry

Biol Mass Spectrom. 1994 Nov;23(11):707-10. doi: 10.1002/bms.1200231110.

Abstract

Herein, we present the first example of charge state specific facile gas-phase cleavage of an aspartic acid-methionine peptide linkage. This cleavage (Asp 75-Met 76) was observed in the alpha-chain of human adult hemoglobin (Hb) and was probed by electrospray ionization mass spectrometry. This specific conformational and/or charge density dependent dissociation was observed primarily in the [M + 11H]11+ and [M + 12H]12+ species. A mechanism involving an intramolecular proton transfer from the protonated carboxyl side chain of Asp 75 to the neighboring Met 76 residue yielding an anhydride moiety at the C-terminal of the Asp 75 is proposed. Dramatic differences in dissociation of [M + 13H]13+ and [M + 14H]14+ species were observed.

MeSH terms

  • Amino Acid Sequence
  • Apoproteins / analysis*
  • Aspartic Acid / analysis
  • Hemoglobins / analysis*
  • Humans
  • Mass Spectrometry
  • Methionine / analysis
  • Molecular Sequence Data
  • Peptides / analysis

Substances

  • Apoproteins
  • Hemoglobins
  • Peptides
  • apohemoglobin
  • Aspartic Acid
  • Methionine