Investigation of Cysteine Modifications in Recombinant Protein Tetanus Toxoid Heavy Chain Fragment C

J Am Soc Mass Spectrom. 2021 Jul 7;32(7):1837-1840. doi: 10.1021/jasms.1c00075. Epub 2021 Jun 24.

Abstract

For conjugated HIV-1 fusion peptide vaccine development, recombinant Tetanus toxoid heavy chain fragment C (rTTHC) was applied as a carrier protein to boost peptide immunogenicity. Understanding the characteristics of rTTHC is the first step prior to the peptide conjugation. A comprehensive mass spectrometry (MS) characterization was performed on E. coli expressed rTTHC during its purification process. Intact mass along with peptide mapping analysis discovered the existence of three cysteine modification forms: glutathionylation, trisulfide bond modification, and disulfide bond shuffling, in correlation to a three-peak profile during a hydrophobic interaction chromatography (HIC) purification step. Coexistence of these multiple oxidative forms indicated that the active thiols underwent redox reaction in the rTTHC material. Identity confirmation of the rTTHC carrier protein by MS analysis provided pivotal guidance to assess the purification step and helped ensure that vaccine development could proceed.

MeSH terms

  • Cysteine / analysis*
  • Cysteine / chemistry
  • Mass Spectrometry / methods*
  • Peptide Fragments / analysis
  • Peptide Fragments / chemistry
  • Recombinant Proteins / analysis*
  • Recombinant Proteins / chemistry
  • Tetanus Toxoid / analysis*
  • Tetanus Toxoid / chemistry

Substances

  • Peptide Fragments
  • Recombinant Proteins
  • Tetanus Toxoid
  • Cysteine