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Scalable, Robust and Highly Productive Novel Convecdiff Membrane Platform for mAb Capture
The recombinant monoclonal antibody capture step represents the current bottleneck in downstream processing. Protein A resins are diffusion-limited chromatography materials which require low flow rates to achieve a binding capacity above 30 g L(−1) with the result of low productivity. Here, we prese...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316305/ https://www.ncbi.nlm.nih.gov/pubmed/35877882 http://dx.doi.org/10.3390/membranes12070677 |
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author | Grünberg, Mario Kuchemüller, Kim B. Töppner, Katrin Busse, Ricarda A. |
author_facet | Grünberg, Mario Kuchemüller, Kim B. Töppner, Katrin Busse, Ricarda A. |
author_sort | Grünberg, Mario |
collection | PubMed |
description | The recombinant monoclonal antibody capture step represents the current bottleneck in downstream processing. Protein A resins are diffusion-limited chromatography materials which require low flow rates to achieve a binding capacity above 30 g L(−1) with the result of low productivity. Here, we present a novel chromatography membrane combining superior binding capacities with high flow rates for high productivity while achieving comparable product quality as state-of-the-art protein A resins. Further, we demonstrate full scalability of this convecdiff technology with experimental data demonstrating suitability for bioprocessing at different scales. This technology results in more than 10-fold higher productivity compared to Protein A resins, which is maintained during scale up. We demonstrate the influence of residence times, feed titers and the cleaning regime on productivity and indicate optimal utilization of the convecdiff membrane based on feed titer availability. The underlying high productivity and short cycle times of this material enable the purification of monoclonal antibodies with 10-times less chromatography material used per batch and utilization of the membrane within one batch. Provided in disposable consumables, this novel technology will remove column handling in bioprocesses and resin re-use over multiple batches. |
format | Online Article Text |
id | pubmed-9316305 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93163052022-07-27 Scalable, Robust and Highly Productive Novel Convecdiff Membrane Platform for mAb Capture Grünberg, Mario Kuchemüller, Kim B. Töppner, Katrin Busse, Ricarda A. Membranes (Basel) Article The recombinant monoclonal antibody capture step represents the current bottleneck in downstream processing. Protein A resins are diffusion-limited chromatography materials which require low flow rates to achieve a binding capacity above 30 g L(−1) with the result of low productivity. Here, we present a novel chromatography membrane combining superior binding capacities with high flow rates for high productivity while achieving comparable product quality as state-of-the-art protein A resins. Further, we demonstrate full scalability of this convecdiff technology with experimental data demonstrating suitability for bioprocessing at different scales. This technology results in more than 10-fold higher productivity compared to Protein A resins, which is maintained during scale up. We demonstrate the influence of residence times, feed titers and the cleaning regime on productivity and indicate optimal utilization of the convecdiff membrane based on feed titer availability. The underlying high productivity and short cycle times of this material enable the purification of monoclonal antibodies with 10-times less chromatography material used per batch and utilization of the membrane within one batch. Provided in disposable consumables, this novel technology will remove column handling in bioprocesses and resin re-use over multiple batches. MDPI 2022-06-30 /pmc/articles/PMC9316305/ /pubmed/35877882 http://dx.doi.org/10.3390/membranes12070677 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Grünberg, Mario Kuchemüller, Kim B. Töppner, Katrin Busse, Ricarda A. Scalable, Robust and Highly Productive Novel Convecdiff Membrane Platform for mAb Capture |
title | Scalable, Robust and Highly Productive Novel Convecdiff Membrane Platform for mAb Capture |
title_full | Scalable, Robust and Highly Productive Novel Convecdiff Membrane Platform for mAb Capture |
title_fullStr | Scalable, Robust and Highly Productive Novel Convecdiff Membrane Platform for mAb Capture |
title_full_unstemmed | Scalable, Robust and Highly Productive Novel Convecdiff Membrane Platform for mAb Capture |
title_short | Scalable, Robust and Highly Productive Novel Convecdiff Membrane Platform for mAb Capture |
title_sort | scalable, robust and highly productive novel convecdiff membrane platform for mab capture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316305/ https://www.ncbi.nlm.nih.gov/pubmed/35877882 http://dx.doi.org/10.3390/membranes12070677 |
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