nES-DMA with Charge-reduction based on Soft X-ray Radiation: Analysis of a Recombinant Monoclonal Antibody

J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Oct 1:1182:122925. doi: 10.1016/j.jchromb.2021.122925. Epub 2021 Sep 20.

Abstract

Due to the fast growing importance of monoclonal antibodies in biomedical research, bioanalytics and human therapy, sensitive, fast and reliable methods are needed to monitor their production, target their characteristics, and for their final quality control. Application of a nano electrospray (nES) with soft X-ray radiation (SXR) based charge reduction and differential mobility analysis (DMA, aka nano electrospray gas-phase electrophoretic mobility molecular analysis, nES GEMMA) allows the size-separation and detection of macromolecules and (bio-)nanoparticles from a few nm up to several hundreds of nm in diameter in a native-like environment. The current study focuses on the analysis of a 148 kDa recombinant monoclonal antibody (rmAb) with the above mentioned instrumental setup and applying an universal detector, i.e. a water-based condensation particle detector (CPC). Next to the intact rmAb, its aggregates and fragment products after digestion with IdeS protease were analyzed. Additionally, influence of temperature treatment and pH variation on the stability of the rmAb was monitored. In this context, changes in electrophoretic mobility diameter (EMD) values, peak shape, and signal intensity based on particle numbers were of interest. Molecular weights calculated by application of a correlation derived from respective standard protein compounds were compared to mass spectrometric values and were found to be in good accordance. To conclude, we demonstrate that nES-DMA is a valuable tool in the characterization and quality control of rmABs.

Keywords: Differential mobility analysis; Gas-phase electrophoresis; IdeS; Recombinant monoclonal antibody; nES GEMMA.

MeSH terms

  • Antibodies, Monoclonal* / analysis
  • Antibodies, Monoclonal* / chemistry
  • Electrophoresis / methods*
  • Ion Mobility Spectrometry / methods*
  • Nanoparticles / chemistry*
  • Particle Size
  • Recombinant Proteins* / analysis
  • Recombinant Proteins* / chemistry
  • X-Rays

Substances

  • Antibodies, Monoclonal
  • Recombinant Proteins