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Development of an insect cell-based adeno-associated virus packaging cell line employing advanced Rep gene expression control system
The insect cell-based baculovirus expression vector (BEV) system is a leading platform for scalable production of adeno-associated viruses (AAVs). The previously described One-Bac system consists of an insect packaging cell line harboring the AAV Rep and Cap genes and a BEV carrying the transgene an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661643/ https://www.ncbi.nlm.nih.gov/pubmed/36381303 http://dx.doi.org/10.1016/j.omtm.2022.10.015 |
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author | Moreno, Fiona Lip, Florence Rojas, Hugo Anggakusuma |
author_facet | Moreno, Fiona Lip, Florence Rojas, Hugo Anggakusuma |
author_sort | Moreno, Fiona |
collection | PubMed |
description | The insect cell-based baculovirus expression vector (BEV) system is a leading platform for scalable production of adeno-associated viruses (AAVs). The previously described One-Bac system consists of an insect packaging cell line harboring the AAV Rep and Cap genes and a BEV carrying the transgene and AAV inverted terminal repeats. Here we describe a new system where we successfully translated the molecular design of a double AAV Rep expression cassette to inducible plasmid vectors. These optimized plasmid vectors employ non-canonical late promoters and alternative start codons that alleviate promoter-promoter competition. Because too much Rep expression can be toxic to the host cells, tighter regulation of AAV Rep expression is warranted. This has been achieved by adopting alternate baculovirus homologous region enhancers. Inoculation of the resultant stable insect Rep packaging cell line by a recombinant BEV produced high-titer recombinant AAV (rAAV) preparations (1 × 10(11) genome copies/mL). Sequential batch reactor experiments indicate that this system is amenable to large-scale AAV production. We generated an insect packaging cell line that employs an optimized Rep gene control system, ensuring stable and appropriate Rep expression. This platform produces potent and high-yield AAV particles and demonstrates potential for scale up. |
format | Online Article Text |
id | pubmed-9661643 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-96616432022-11-14 Development of an insect cell-based adeno-associated virus packaging cell line employing advanced Rep gene expression control system Moreno, Fiona Lip, Florence Rojas, Hugo Anggakusuma Mol Ther Methods Clin Dev Original Article The insect cell-based baculovirus expression vector (BEV) system is a leading platform for scalable production of adeno-associated viruses (AAVs). The previously described One-Bac system consists of an insect packaging cell line harboring the AAV Rep and Cap genes and a BEV carrying the transgene and AAV inverted terminal repeats. Here we describe a new system where we successfully translated the molecular design of a double AAV Rep expression cassette to inducible plasmid vectors. These optimized plasmid vectors employ non-canonical late promoters and alternative start codons that alleviate promoter-promoter competition. Because too much Rep expression can be toxic to the host cells, tighter regulation of AAV Rep expression is warranted. This has been achieved by adopting alternate baculovirus homologous region enhancers. Inoculation of the resultant stable insect Rep packaging cell line by a recombinant BEV produced high-titer recombinant AAV (rAAV) preparations (1 × 10(11) genome copies/mL). Sequential batch reactor experiments indicate that this system is amenable to large-scale AAV production. We generated an insect packaging cell line that employs an optimized Rep gene control system, ensuring stable and appropriate Rep expression. This platform produces potent and high-yield AAV particles and demonstrates potential for scale up. American Society of Gene & Cell Therapy 2022-10-28 /pmc/articles/PMC9661643/ /pubmed/36381303 http://dx.doi.org/10.1016/j.omtm.2022.10.015 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Article Moreno, Fiona Lip, Florence Rojas, Hugo Anggakusuma Development of an insect cell-based adeno-associated virus packaging cell line employing advanced Rep gene expression control system |
title | Development of an insect cell-based adeno-associated virus packaging cell line employing advanced Rep gene expression control system |
title_full | Development of an insect cell-based adeno-associated virus packaging cell line employing advanced Rep gene expression control system |
title_fullStr | Development of an insect cell-based adeno-associated virus packaging cell line employing advanced Rep gene expression control system |
title_full_unstemmed | Development of an insect cell-based adeno-associated virus packaging cell line employing advanced Rep gene expression control system |
title_short | Development of an insect cell-based adeno-associated virus packaging cell line employing advanced Rep gene expression control system |
title_sort | development of an insect cell-based adeno-associated virus packaging cell line employing advanced rep gene expression control system |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9661643/ https://www.ncbi.nlm.nih.gov/pubmed/36381303 http://dx.doi.org/10.1016/j.omtm.2022.10.015 |
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