CDL Collaboration Information

Collaboration for cutting-edge biosimilar characterization

Thermo Fisher Scientific has been working with the Christian Doppler Laboratory for Innovative Tools for Biosimilar Characterization (CDL) at the University of Salzburg, Austria and other corporate members since 2013 to co-develop a toolkit of new/novel and appropriate methods and workflows for the analysis of biosimilar drug molecules. The collaboration aims to:

Christian Doppler Laboratory for Innovative Tools for Biosimilar Characterization (CDL) group photo
  • Accelerate innovations in biopharmaceutical characterization
  • Translate biosimilar research into transferable, routine, compliant solutions
  • Develop workflows which are appropriate for biosimilar characterisation
  • Gain insights, understanding and alignment with the regulatory requirements for biosimilars
  • Mentor and develop the next generation of biopharmaceutical analytical scientists
   Video detailing the work of the CDL and the collaboration

Native mass spectrometry combined with enzymatic dissection unravels glycoform heterogeneity of biopharmaceuticals

Robust manufacturing processes resulting in consistent glycosylation are critical for the efficacy and safety of biopharmaceuticals. Information on glycosylation can be obtained by conventional bottom–up methods but is often limited to the glycan or glycopeptide level. In this seminal publication researchers from the CDL detail the application of high-resolution native mass spectrometry (MS) for the characterization of the therapeutic fusion protein Etanercept, unravelling glycoform heterogeneity in conditions of hitherto unmatched mass spectral complexity.

Higher spatial resolution at lower charge states, an inherent characteristic of native MS, represents a key component for the successful revelation of glycan heterogeneity. Combined with enzymatic dissection using a set of proteases and glycosidases, assignment of specific glycoforms was achieved by transferring information from the subunit to the whole protein level. The application of native mass spectrometric analysis of intact Etanercept as a fingerprinting tool for the assessment of batch-to-batch variability is exemplified and its usage in demonstrating comparability after changes in the biologic manufacturing process is suggested.


Piecing together protein analysis


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