Epi‐CHO, an episomal expression system for recombinant protein production in CHO cells
Epi-CHO — эписомная система экспрессии для получения рекомбинантных белков в клетках CHO
2005-06-09
SCID: 54.1/ph8sgvpy
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CHO cellsEpi-CHO expression systemPolyomavirus large T antigenepisomal plasmid amplificationrecombinant protein production
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Abstract (AI)
This study describes the development of a transient expression system for CHO cells based on autonomous replication and retention of transfected plasmid DNA. A transient expression system that allows extrachromosomal amplification of plasmids permits more plasmid copies to persist in the transfected cell throughout the production phase leading to a significant increase in transgene expression. The expression system, named Epi-CHO comprises (1) a CHO-K1 cell line stably transfected with the Polyomavirus (Py) large T (LT) antigen gene (PyLT) and (2) a DNA expression vector, pPyEBV encoding the Py origin (PyOri) for autonomous plasmid amplification and encoding Epstein-Barr Virus (EBV) nuclear antigen-1 (EBNA-1) and OriP for plasmid retention. The CHO-K1 cell line expressing PyLT, named CHO-T was adapted to suspension growth in serum-free media to facilitate large-scale transient transfection and recombinant gene expression. Enhanced green fluorescent protein (EGFP) and human growth hormone (hGH) were used as reporter proteins to demonstrate transgene expression and productivity. Transfection of suspension-growing CHO-T cells with the vector pPyEBV encoding hGH resulted in a final concentration of 75 mg L(-1) of hGH in culture supernatants 11 days following transfection.
Key Findings
1
Developed Epi-CHO, a transient CHO expression system enabling autonomous plasmid amplification and episomal retention during recombinant protein production.
2
EGFP and human growth hormone demonstrated successful transgene expression using the Epi-CHO system.
3
Epi-CHO combines CHO-K1 cells stably expressing Polyomavirus large T antigen with pPyEBV vectors carrying PyOri, EBNA-1, and OriP.
4
The engineered CHO-T cells were adapted to suspension growth in serum-free medium, supporting large-scale transient transfection and protein expression.
5
Transfection with an hGH-encoding pPyEBV vector produced 75 mg L−1 hGH in culture supernatants 11 days after transfection.
Research Object
Epi-CHO episomal expression system in suspension-adapted CHO-T cells for recombinant protein production
Research Subject
Autonomous plasmid amplification and retention and their effects on transgene expression and recombinant protein productivity
Publication Details
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2005-06-09
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