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An integrated and continuous downstream process for microbial virus‐like particle vaccine biomanufacture
In this study, we present the first integrated and continuous downstream process for the production of microbial virus‐like particle vaccines. Modular murine polyomavirus major capsid VP1 with integrated J8 antigen was used as a model virus‐like particle vaccine. The integrated continuous downstream...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542101/ https://www.ncbi.nlm.nih.gov/pubmed/35478403 http://dx.doi.org/10.1002/bit.28118 |
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author | Gerstweiler, Lukas Billakanti, Jagan Bi, Jingxiu Middelberg, Anton P. J. |
author_facet | Gerstweiler, Lukas Billakanti, Jagan Bi, Jingxiu Middelberg, Anton P. J. |
author_sort | Gerstweiler, Lukas |
collection | PubMed |
description | In this study, we present the first integrated and continuous downstream process for the production of microbial virus‐like particle vaccines. Modular murine polyomavirus major capsid VP1 with integrated J8 antigen was used as a model virus‐like particle vaccine. The integrated continuous downstream process starts with crude cell lysate and consists of a flow‐through chromatography step followed by periodic counter‐current chromatography (PCC) (bind‐elute) using salt‐tolerant mixed‐mode resin and subsequent in‐line assembly. The automated process showed a robust behavior over different inlet feed concentrations ranging from 1.0 to 3.2 mg ml(−1) with only minimal adjustments needed, and produced continuously high‐quality virus‐like particles, free of nucleic acids, with constant purity over extended periods of time. The average size remained constant between 44.8 ± 2.3 and 47.2 ± 2.9 nm comparable to literature. The process had an overall product recovery of 88.6% and a process productivity up to 2.56 mg h(−1) ml(resin) (−1) in the PCC step, depending on the inlet concentration. Integrating a flow through step with a subsequent PCC step allowed streamlined processing, showing a possible continuous pathway for a wide range of products of interest. |
format | Online Article Text |
id | pubmed-9542101 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95421012022-10-14 An integrated and continuous downstream process for microbial virus‐like particle vaccine biomanufacture Gerstweiler, Lukas Billakanti, Jagan Bi, Jingxiu Middelberg, Anton P. J. Biotechnol Bioeng ARTICLES In this study, we present the first integrated and continuous downstream process for the production of microbial virus‐like particle vaccines. Modular murine polyomavirus major capsid VP1 with integrated J8 antigen was used as a model virus‐like particle vaccine. The integrated continuous downstream process starts with crude cell lysate and consists of a flow‐through chromatography step followed by periodic counter‐current chromatography (PCC) (bind‐elute) using salt‐tolerant mixed‐mode resin and subsequent in‐line assembly. The automated process showed a robust behavior over different inlet feed concentrations ranging from 1.0 to 3.2 mg ml(−1) with only minimal adjustments needed, and produced continuously high‐quality virus‐like particles, free of nucleic acids, with constant purity over extended periods of time. The average size remained constant between 44.8 ± 2.3 and 47.2 ± 2.9 nm comparable to literature. The process had an overall product recovery of 88.6% and a process productivity up to 2.56 mg h(−1) ml(resin) (−1) in the PCC step, depending on the inlet concentration. Integrating a flow through step with a subsequent PCC step allowed streamlined processing, showing a possible continuous pathway for a wide range of products of interest. John Wiley and Sons Inc. 2022-05-10 2022-08 /pmc/articles/PMC9542101/ /pubmed/35478403 http://dx.doi.org/10.1002/bit.28118 Text en © 2022 The Authors. Biotechnology and Bioengineering published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | ARTICLES Gerstweiler, Lukas Billakanti, Jagan Bi, Jingxiu Middelberg, Anton P. J. An integrated and continuous downstream process for microbial virus‐like particle vaccine biomanufacture |
title | An integrated and continuous downstream process for microbial virus‐like particle vaccine biomanufacture |
title_full | An integrated and continuous downstream process for microbial virus‐like particle vaccine biomanufacture |
title_fullStr | An integrated and continuous downstream process for microbial virus‐like particle vaccine biomanufacture |
title_full_unstemmed | An integrated and continuous downstream process for microbial virus‐like particle vaccine biomanufacture |
title_short | An integrated and continuous downstream process for microbial virus‐like particle vaccine biomanufacture |
title_sort | integrated and continuous downstream process for microbial virus‐like particle vaccine biomanufacture |
topic | ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9542101/ https://www.ncbi.nlm.nih.gov/pubmed/35478403 http://dx.doi.org/10.1002/bit.28118 |
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