Factors affecting product association as a mechanism of host-cell protein persistence in bioprocessing
| Author(s) | Oh, Young Hoon | |
| Author(s) | Becker, Matthew L. | |
| Author(s) | Mendola, Kerri M. | |
| Author(s) | Choe, Leila H. | |
| Author(s) | Min, Lie | |
| Author(s) | Lee, Kelvin H. | |
| Author(s) | Yigzaw, Yinges | |
| Author(s) | Seay, Alexander | |
| Author(s) | Bill, Jerome | |
| Author(s) | Li, Xuanwen | |
| Author(s) | Roush, David J. | |
| Author(s) | Cramer, Steven M. | |
| Author(s) | Menegatti, Stefano | |
| Author(s) | Lenhoff, Abraham M. | |
| Date Accessioned | 2024-04-16T13:53:27Z | |
| Date Available | 2024-04-16T13:53:27Z | |
| Publication Date | 2024-01-19 | |
| Description | This is the peer reviewed version of the following article: Oh, Y. H., Becker, M. L., Mendola, K. M., Choe, L. H., Min, L., Lee, K. H., Yigzaw, Y., Seay, A., Bill, J., Li, X., Roush, D. J., Cramer, S. M., Menegatti, S., & Lenhoff, A. M. (2024). Factors affecting product association as a mechanism of host-cell protein persistence in bioprocessing. Biotechnology and Bioengineering, 121, 1283–1296. https://doi.org/10.1002/bit.28658, which has been published in final form at https://doi.org/10.1002/bit.28658. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. This article may not be enhanced, enriched or otherwise transformed into a derivative work, without express permission from Wiley or by statutory rights under applicable legislation. Copyright notices must not be removed, obscured or modified. The article must be linked to Wiley’s version of record on Wiley Online Library and any embedding, framing or otherwise making available the article or pages thereof by third parties from platforms, services and websites other than Wiley Online Library must be prohibited. © 2024 Wiley Periodicals LLC. This article will be embargoed until 01/19/2025. | |
| Abstract | Product association of host-cell proteins (HCPs) to monoclonal antibodies (mAbs) is widely regarded as a mechanism that can enable HCP persistence through multiple purification steps and even into the final drug substance. Discussion of this mechanism often implies that the existence or extent of persistence is directly related to the strength of binding but actual measurements of the binding affinity of such interactions remain sparse. Two separate avenues of investigation of HCP-mAb binding are reported here. One is the measurement of the affinity of binding of individual, commonly persistent Chinese hamster ovary (CHO) HCPs to each of a set of mAbs, and the other uses quantitative proteomic measurements to assess binding of HCPs in a null CHO harvested cell culture fluid (HCCF) to mAbs produced in the same cell line. The individual HCP measurements show that the binding affinities of individual HCPs to different mAbs can vary appreciably but are rarely very high, with only weak pH dependence. The measurements on the null HCCF allow estimation of individual HCP-mAb affinities; these are typically weaker than those seen in affinity measurements on isolated HCPs. Instead, the extent of binding appears correlated with the initial abundance of individual HCPs in the HCCF and the forms of the HCPs in the solution, i.e., whether HCPs are present as free molecules or as parts of large aggregates. Separate protein A chromatography experiments performed by feeding different fractions of a mAb-containing HCCF obtained by size-exclusion chromatography (SEC) showed clear differences in the number and identity of HCPs found in the protein A eluate. These results indicate a significant role for HCP-mAb association in determining HCP persistence through protein A chromatography, presumably through binding of HCP-mAb complexes to the resin. Overall, the results illustrate the importance of considering more fully the biophysical context of HCP-product association in assessing the factors that may affect the phenomenon and determine its implications. Knowledge of the abundances and the forms of individual or aggregated HCPs in HCCF are particularly significant, emphasizing the integration of upstream and downstream bioprocessing and the importance of understanding the collective properties of HCPs in addition to just the biophysical properties of individual HCPs. | |
| Sponsor | This work was performed under a Project Award Agreement from the National Institute for Innovation in Manufacturing Biopharmaceuticals (NIIMBL) and financial assistance award 70NANB21H002 from the U.S. Department of Commerce, National Institute of Standards and Technology. | |
| Citation | Oh, Y. H., Becker, M. L., Mendola, K. M., Choe, L. H., Min, L., Lee, K. H., Yigzaw, Y., Seay, A., Bill, J., Li, X., Roush, D. J., Cramer, S. M., Menegatti, S., & Lenhoff, A. M. (2024). Factors affecting product association as a mechanism of host-cell protein persistence in bioprocessing. Biotechnology and Bioengineering, 121, 1283–1296. https://doi.org/10.1002/bit.28658 | |
| ISSN | 1097-0290 | |
| URL | https://udspace.udel.edu/handle/19716/34285 | |
| Language | en_US | |
| Publisher | Biotechnology and Bioengineering | |
| Keywords | dissociation constant | |
| Keywords | host-cell protein | |
| Keywords | monoclonal antibody | |
| Keywords | product association | |
| Keywords | protein A chromatography | |
| Title | Factors affecting product association as a mechanism of host-cell protein persistence in bioprocessing | |
| Type | Article |
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