Cargando…
Novel application of anti‐human Fc nanobody for screening high‐producing CHO cells for monoclonal antibody
Animal‐derived anti‐IgG secondary antibodies are currently employed to stain and screen of human monoclonal antibody(mAb)‐producing cells, but using animal‐derived antibodies may raise the concerns of high cost, complicated operations and biological safety issues in biopharmaceutical manufacturing....
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550735/ https://www.ncbi.nlm.nih.gov/pubmed/36247827 http://dx.doi.org/10.1002/elsc.202200028 |
_version_ | 1784805946962214912 |
---|---|
author | Zhu, Di Wang, Zheng Xu, Yunxia Lin, Jing Qiu, Mei Liu, Jianghai Li, Xinlei |
author_facet | Zhu, Di Wang, Zheng Xu, Yunxia Lin, Jing Qiu, Mei Liu, Jianghai Li, Xinlei |
author_sort | Zhu, Di |
collection | PubMed |
description | Animal‐derived anti‐IgG secondary antibodies are currently employed to stain and screen of human monoclonal antibody(mAb)‐producing cells, but using animal‐derived antibodies may raise the concerns of high cost, complicated operations and biological safety issues in biopharmaceutical manufacturing. Nanobodies(VHHs) are attractive forms of antibodies for their straightforward engineering and expression in both eukaryotic and prokaryotic systems. Using phage‐displayed immune llama VHH library, we identified new anti‐Fc VHHs that could bind to human Fc with high affinity. In GFP fusion format, the anti‐Fc VHH‐GFP generated dramatically stronger FACS signals than AF488 conjugated anti‐IgG antibodies when used for staining mAb‐producing CHO cells. Furthermore, preparative sorting of CHO cells based on anti‐Fc VHH‐GFP staining resulted in the enrichment of cell lines capable of synthesizing mAb at high productivity. This safe and cost‐efficient anti‐Fc VHH‐GFP may optimize the process of generating highly productive cell lines for therapeutic mAb production compared to conventional animal‐derived fluorescent antibodies. |
format | Online Article Text |
id | pubmed-9550735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-95507352022-10-14 Novel application of anti‐human Fc nanobody for screening high‐producing CHO cells for monoclonal antibody Zhu, Di Wang, Zheng Xu, Yunxia Lin, Jing Qiu, Mei Liu, Jianghai Li, Xinlei Eng Life Sci Research Articles Animal‐derived anti‐IgG secondary antibodies are currently employed to stain and screen of human monoclonal antibody(mAb)‐producing cells, but using animal‐derived antibodies may raise the concerns of high cost, complicated operations and biological safety issues in biopharmaceutical manufacturing. Nanobodies(VHHs) are attractive forms of antibodies for their straightforward engineering and expression in both eukaryotic and prokaryotic systems. Using phage‐displayed immune llama VHH library, we identified new anti‐Fc VHHs that could bind to human Fc with high affinity. In GFP fusion format, the anti‐Fc VHH‐GFP generated dramatically stronger FACS signals than AF488 conjugated anti‐IgG antibodies when used for staining mAb‐producing CHO cells. Furthermore, preparative sorting of CHO cells based on anti‐Fc VHH‐GFP staining resulted in the enrichment of cell lines capable of synthesizing mAb at high productivity. This safe and cost‐efficient anti‐Fc VHH‐GFP may optimize the process of generating highly productive cell lines for therapeutic mAb production compared to conventional animal‐derived fluorescent antibodies. John Wiley and Sons Inc. 2022-08-23 /pmc/articles/PMC9550735/ /pubmed/36247827 http://dx.doi.org/10.1002/elsc.202200028 Text en © 2022 The Authors. Engineering in Life Sciences published by Wiley‐VCH GmbH. 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 | Research Articles Zhu, Di Wang, Zheng Xu, Yunxia Lin, Jing Qiu, Mei Liu, Jianghai Li, Xinlei Novel application of anti‐human Fc nanobody for screening high‐producing CHO cells for monoclonal antibody |
title | Novel application of anti‐human Fc nanobody for screening high‐producing CHO cells for monoclonal antibody |
title_full | Novel application of anti‐human Fc nanobody for screening high‐producing CHO cells for monoclonal antibody |
title_fullStr | Novel application of anti‐human Fc nanobody for screening high‐producing CHO cells for monoclonal antibody |
title_full_unstemmed | Novel application of anti‐human Fc nanobody for screening high‐producing CHO cells for monoclonal antibody |
title_short | Novel application of anti‐human Fc nanobody for screening high‐producing CHO cells for monoclonal antibody |
title_sort | novel application of anti‐human fc nanobody for screening high‐producing cho cells for monoclonal antibody |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9550735/ https://www.ncbi.nlm.nih.gov/pubmed/36247827 http://dx.doi.org/10.1002/elsc.202200028 |
work_keys_str_mv | AT zhudi novelapplicationofantihumanfcnanobodyforscreeninghighproducingchocellsformonoclonalantibody AT wangzheng novelapplicationofantihumanfcnanobodyforscreeninghighproducingchocellsformonoclonalantibody AT xuyunxia novelapplicationofantihumanfcnanobodyforscreeninghighproducingchocellsformonoclonalantibody AT linjing novelapplicationofantihumanfcnanobodyforscreeninghighproducingchocellsformonoclonalantibody AT qiumei novelapplicationofantihumanfcnanobodyforscreeninghighproducingchocellsformonoclonalantibody AT liujianghai novelapplicationofantihumanfcnanobodyforscreeninghighproducingchocellsformonoclonalantibody AT lixinlei novelapplicationofantihumanfcnanobodyforscreeninghighproducingchocellsformonoclonalantibody |