Ready for the Real-World: Middle-Down Analysis for Cell Line Optimization

Event Overview:

In biotherapeutic development, changing cell culture conditions is necessary to enable simpler, faster and more cost-effective drug delivery to patients. These changes, however, can induce cellular stress and adversely impact product quality, creating additional challenges in manufacturing.
Reliable and streamlined workflows to characterize post-translational modifications (PTMs) are necessary to create a comprehensive molecular profile of a biopharmaceutical. Adopting workflows that provide these critical pieces of information with minimal processing steps allows for less labor intensive characterization of PTMs and reduces the risk of introducing artificial PTMs or other undesirable modifications.

Key Learning Objectives:

Improve cell line optimization using middle-down fragment analysis
Achieve comprehensive structural confirmation of engineered disulfides with middle-down analysis
Explore the benefits of subunit workflows for cell line screening

Who Should Attend:

Scientists
Senior Scientists and Directors in Cell Line Development
Cell Line Engineering and Protein Characterization Groups

Featured Speaker

Hirsh Nanda

Director, Analytical Sciences

J&J Innovative Medicines

Hirsh Nanda is the Director of Analytical Sciences at Johnson & Johnson Innovative Medicines. Hirsh joined J&J in 2015. In his current role, he leads an Analytical Sciences group supporting research and development of biologic therapeutics, including cell line engineering and development. His team performs in-depth mass spectroscopy and biophysical characterization across modalities and next-generation therapies.

For any technical questions, please contact Nicole Valle: nvalle@mjhevents.com

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Ready for the Real-World: Middle-Down Analysis for Cell Line Optimization

This event is now available on demand.

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