Pilot‐scale process for magnetic bead purification of antibodies directly from non‐clarified CHO cell culture

• Published in: Biotechnology progress Vol. 35; no. 3; pp. e2775 - n/a
• Main Authors: Brechmann, Nils A., Eriksson, Per‐Olov, Eriksson, Kristofer, Oscarsson, Sven, Buijs, Jos, Shokri, Atefeh, Hjälm, Göran, Chotteau, Véronique
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.05.2019; Wiley Subscription Services, Inc
• Subjects: Adsorption; Animals; Antibodies, Monoclonal - chemistry; Antibodies, Monoclonal - metabolism; Beads; Biotechnology; Bioteknologi; Cell culture; CHO Cells - metabolism; Chromatography; Chromatography, Affinity - instrumentation; Chromatography, Affinity - methods; Column chromatography; Cricetulus; downstream-bioprocess; Hydrogen-Ion Concentration; Immunoglobulin G; magnetic beads; Magnetic separators; Magnetics - instrumentation; Magnetics - methods; Monoclonal antibodies; monoclonal antibody; Organic chemistry; pilot-scale; Protein A; Proteins; Purification; Separation; Separators; Staphylococcal Protein A - chemistry; magnetic beads; pilot-scale; downstream-bioprocess; monoclonal antibody; purification
• ISSN: 8756-7938; 1520-6033; 1520-6033
• DOI: 10.1002/btpr.2775

High capacity magnetic protein A agarose beads, LOABeads PrtA, were used in the development of a new process for affinity purification of monoclonal antibodies (mAbs) from non‐clarified CHO cell broth using a pilot‐scale magnetic separator. The LOABeads had a maximum binding capacity of 65 mg/mL and an adsorption capacity of 25–42 mg IgG/mL bead in suspension for an IgG concentration of 1 to 8 g/L. Pilot‐scale separation was initially tested in a mAb capture step from 26 L clarified harvest. Small‐scale experiments showed that similar mAb adsorptions were obtained in cell broth containing 40 × 106 cells/mL as in clarified supernatant. Two pilot‐scale purification runs were then performed on non‐clarified cell broth from fed‐batch runs of 16 L, where a rapid mAb adsorption ≥96.6% was observed after 1 h. This process using 1 L of magnetic beads had an overall mAb yield of 86% and 16 times concentration factor. After this single protein A capture step, the mAb purity was similar to the one obtained by column chromatography, while the host cell protein content was very low, <10 ppm. Our results showed that this magnetic bead mAb purification process, using a dedicated pilot‐scale separation device, was a highly efficient single step, which directly connected the culture to the downstream process without cell clarification. Purification of mAb directly from non‐clarified cell broth without cell separation can provide significant savings in terms of resources, operation time, and equipment, compared to legacy procedure of cell separation followed by column chromatography step. © 2019 American Institute of Chemical Engineers Biotechnol. Prog., 35: e2775, 2019.