Cargando…

Continuous capture of recombinant antibodies by ZnCl(2) precipitation without polyethylene glycol

The capture of recombinant antibodies from cell culture broth is the first critical step of downstream processing. We were able to develop a precipitation‐based method for the capture and purification of monoclonal antibodies based on divalent cations, namely ZnCl(2). Traditional precipitation proce...

Descripción completa

Detalles Bibliográficos
Autores principales: Dutra, Gregory, Komuczki, Daniel, Jungbauer, Alois, Satzer, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336134/
https://www.ncbi.nlm.nih.gov/pubmed/32647505
http://dx.doi.org/10.1002/elsc.201900160
_version_ 1783554255284600832
author Dutra, Gregory
Komuczki, Daniel
Jungbauer, Alois
Satzer, Peter
author_facet Dutra, Gregory
Komuczki, Daniel
Jungbauer, Alois
Satzer, Peter
author_sort Dutra, Gregory
collection PubMed
description The capture of recombinant antibodies from cell culture broth is the first critical step of downstream processing. We were able to develop a precipitation‐based method for the capture and purification of monoclonal antibodies based on divalent cations, namely ZnCl(2). Traditional precipitation processes have to deal with high dilution factors especially for resolubilization and higher viscosity due to the use of PEG as precipitation or co‐precipitation agent. By the use of the crosslinking nature of divalent cations without the use of PEG, we kept viscosity from the supernatant and resolubilization dilution factors very low. This is especially beneficial for the solid–liquid separation for the harvest and wash of the precipitate in continuous mode. For this harvest and wash, we used tangential flow filtration that benefits a lot from low viscosity solutions, which minimizes the membrane fouling. With this precipitation based on ZnCl(2,) we were able to implement a very lean and efficient process. We demonstrated precipitation studies with three different antibodies, Adalimumab, Trastuzumab, and Denosumab, and a continuous capture case study using tangential flow filtration for precipitate recovery. In this study, we achieved yields of 70%.
format Online
Article
Text
id pubmed-7336134
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-73361342020-07-08 Continuous capture of recombinant antibodies by ZnCl(2) precipitation without polyethylene glycol Dutra, Gregory Komuczki, Daniel Jungbauer, Alois Satzer, Peter Eng Life Sci Research Articles The capture of recombinant antibodies from cell culture broth is the first critical step of downstream processing. We were able to develop a precipitation‐based method for the capture and purification of monoclonal antibodies based on divalent cations, namely ZnCl(2). Traditional precipitation processes have to deal with high dilution factors especially for resolubilization and higher viscosity due to the use of PEG as precipitation or co‐precipitation agent. By the use of the crosslinking nature of divalent cations without the use of PEG, we kept viscosity from the supernatant and resolubilization dilution factors very low. This is especially beneficial for the solid–liquid separation for the harvest and wash of the precipitate in continuous mode. For this harvest and wash, we used tangential flow filtration that benefits a lot from low viscosity solutions, which minimizes the membrane fouling. With this precipitation based on ZnCl(2,) we were able to implement a very lean and efficient process. We demonstrated precipitation studies with three different antibodies, Adalimumab, Trastuzumab, and Denosumab, and a continuous capture case study using tangential flow filtration for precipitate recovery. In this study, we achieved yields of 70%. John Wiley and Sons Inc. 2020-03-24 /pmc/articles/PMC7336134/ /pubmed/32647505 http://dx.doi.org/10.1002/elsc.201900160 Text en © 2020 The Authors. Engineering in Life Sciences published by Wiley‐VCH Verlag GmbH & Co. KGaA This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Dutra, Gregory
Komuczki, Daniel
Jungbauer, Alois
Satzer, Peter
Continuous capture of recombinant antibodies by ZnCl(2) precipitation without polyethylene glycol
title Continuous capture of recombinant antibodies by ZnCl(2) precipitation without polyethylene glycol
title_full Continuous capture of recombinant antibodies by ZnCl(2) precipitation without polyethylene glycol
title_fullStr Continuous capture of recombinant antibodies by ZnCl(2) precipitation without polyethylene glycol
title_full_unstemmed Continuous capture of recombinant antibodies by ZnCl(2) precipitation without polyethylene glycol
title_short Continuous capture of recombinant antibodies by ZnCl(2) precipitation without polyethylene glycol
title_sort continuous capture of recombinant antibodies by zncl(2) precipitation without polyethylene glycol
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7336134/
https://www.ncbi.nlm.nih.gov/pubmed/32647505
http://dx.doi.org/10.1002/elsc.201900160
work_keys_str_mv AT dutragregory continuouscaptureofrecombinantantibodiesbyzncl2precipitationwithoutpolyethyleneglycol
AT komuczkidaniel continuouscaptureofrecombinantantibodiesbyzncl2precipitationwithoutpolyethyleneglycol
AT jungbaueralois continuouscaptureofrecombinantantibodiesbyzncl2precipitationwithoutpolyethyleneglycol
AT satzerpeter continuouscaptureofrecombinantantibodiesbyzncl2precipitationwithoutpolyethyleneglycol