Quasi-Steady-State Approach for Efficient Multiscale Simulation and Optimization of mAb Glycosylation in CHO Cell Culture
Yingjie Ma, Jing Guo, Andrew Maloney, and Richard Braatz

TL;DR
This paper introduces a quasi-steady-state (QSS) method that significantly accelerates multiscale glycosylation modeling in mAb production, enabling efficient optimization and control with minimal accuracy loss.
Contribution
The authors develop a novel QSS approach that simplifies complex multiscale models, reducing computational time by over 300 times while maintaining high accuracy.
Findings
QSS method is over 300 times faster than traditional methods.
Relative error of the QSS approach is less than 1.6%.
Enables efficient model-based optimization and control of glycosylation.
Abstract
Glycosylation is a critical quality attribute for monoclonal antibody (mAb) production, influenced by both process conditions and cellular mechanisms. Multiscale mechanistic models, spanning from the bioreactor to the Golgi apparatus, have been proposed for analyzing the glycosylation process. However, these models are computationally intensive to solve when using traditional methods, making optimization and control challenging. In this work, we propose a quasi-steady-state (QSS) approach for efficiently solving the multiscale glycosylation model. By introducing the QSS assumption and assuming negligible nucleotide sugar donor (NSD) flux for glycosylation in the Golgi, the large-scale partial differential algebraic equation system is converted into a series of independent differential algebraic equation systems. Based on that representation, we develop a three-step QSS simulation method…
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Taxonomy
TopicsGlycosylation and Glycoproteins Research · Viral Infectious Diseases and Gene Expression in Insects · Protein purification and stability
