Enhanced expression of codon optimized interferon gamma in CHO cells

The human interferon-gamma (IFN-γ) is a potential drug candidate for treating various diseases due to its immunomodulatory properties. The efficient production of this protein can be achieved through a popular industrial host, Chinese hamster ovary (CHO) cells. However, recombinant expression of for...

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Main Authors: Yusufi, Faraaz N. K., Yang, Yuansheng, Lee, Dong-Yup, Chung, Bevan Kai-Sheng, Mariati
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2016
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Online Access:https://hdl.handle.net/10356/82159
http://hdl.handle.net/10220/41101
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-821592020-03-07T11:35:27Z Enhanced expression of codon optimized interferon gamma in CHO cells Yusufi, Faraaz N. K. Yang, Yuansheng Lee, Dong-Yup Chung, Bevan Kai-Sheng Mariati School of Chemical and Biomedical Engineering Chinese hamster ovary cells Codon optimization The human interferon-gamma (IFN-γ) is a potential drug candidate for treating various diseases due to its immunomodulatory properties. The efficient production of this protein can be achieved through a popular industrial host, Chinese hamster ovary (CHO) cells. However, recombinant expression of foreign proteins is typically suboptimal possibly due to the usage of non-native codon patterns within the coding sequence. Therefore, we demonstrated the application of a recently developed codon optimization approach to design synthetic IFN-γ coding sequences for enhanced heterologous expression in CHO cells. For codon optimization, earlier studies suggested to establish the target usage distribution pattern in terms of selected design parameters such as individual codon usage (ICU) and codon context (CC), mainly based on the host's highly expressed genes. However, our RNA-Seq based transcriptome profiling indicated that the ICU and CC distribution patterns of different gene expression classes in CHO cell are relatively similar, unlike other microbial expression hosts, Escherichia coli and Saccharomyces cerevisiae. This finding was further corroborated through the in vivo expression of various ICU and CC optimized IFN-γ in CHO cells. Interestingly, the CC-optimized genes exhibited at least 13-fold increase in expression level compared to the wild-type IFN-γ while a maximum of 10-fold increase was observed for the ICU-optimized genes. Although design criteria based on individual codons, such as ICU, have been widely used for gene optimization, our experimental results suggested that codon context is relatively more effective parameter for improving recombinant IFN-γ expression in CHO cells. ASTAR (Agency for Sci., Tech. and Research, S’pore) 2016-08-05T06:51:56Z 2019-12-06T14:47:44Z 2016-08-05T06:51:56Z 2019-12-06T14:47:44Z 2013 Journal Article Chung, B. K.-S., Yusufi, F. N. K., Mariati, Yang, Y., & Lee, D.-Y. (2013). Enhanced expression of codon optimized interferon gamma in CHO cells. Journal of Biotechnology, 167(3), 326-333. 0168-1656 https://hdl.handle.net/10356/82159 http://hdl.handle.net/10220/41101 10.1016/j.jbiotec.2013.07.011 en Journal of Biotechnology © 2013 Elsevier B.V. 8 p.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Chinese hamster ovary cells
Codon optimization
spellingShingle Chinese hamster ovary cells
Codon optimization
Yusufi, Faraaz N. K.
Yang, Yuansheng
Lee, Dong-Yup
Chung, Bevan Kai-Sheng
Mariati
Enhanced expression of codon optimized interferon gamma in CHO cells
description The human interferon-gamma (IFN-γ) is a potential drug candidate for treating various diseases due to its immunomodulatory properties. The efficient production of this protein can be achieved through a popular industrial host, Chinese hamster ovary (CHO) cells. However, recombinant expression of foreign proteins is typically suboptimal possibly due to the usage of non-native codon patterns within the coding sequence. Therefore, we demonstrated the application of a recently developed codon optimization approach to design synthetic IFN-γ coding sequences for enhanced heterologous expression in CHO cells. For codon optimization, earlier studies suggested to establish the target usage distribution pattern in terms of selected design parameters such as individual codon usage (ICU) and codon context (CC), mainly based on the host's highly expressed genes. However, our RNA-Seq based transcriptome profiling indicated that the ICU and CC distribution patterns of different gene expression classes in CHO cell are relatively similar, unlike other microbial expression hosts, Escherichia coli and Saccharomyces cerevisiae. This finding was further corroborated through the in vivo expression of various ICU and CC optimized IFN-γ in CHO cells. Interestingly, the CC-optimized genes exhibited at least 13-fold increase in expression level compared to the wild-type IFN-γ while a maximum of 10-fold increase was observed for the ICU-optimized genes. Although design criteria based on individual codons, such as ICU, have been widely used for gene optimization, our experimental results suggested that codon context is relatively more effective parameter for improving recombinant IFN-γ expression in CHO cells.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Yusufi, Faraaz N. K.
Yang, Yuansheng
Lee, Dong-Yup
Chung, Bevan Kai-Sheng
Mariati
format Article
author Yusufi, Faraaz N. K.
Yang, Yuansheng
Lee, Dong-Yup
Chung, Bevan Kai-Sheng
Mariati
author_sort Yusufi, Faraaz N. K.
title Enhanced expression of codon optimized interferon gamma in CHO cells
title_short Enhanced expression of codon optimized interferon gamma in CHO cells
title_full Enhanced expression of codon optimized interferon gamma in CHO cells
title_fullStr Enhanced expression of codon optimized interferon gamma in CHO cells
title_full_unstemmed Enhanced expression of codon optimized interferon gamma in CHO cells
title_sort enhanced expression of codon optimized interferon gamma in cho cells
publishDate 2016
url https://hdl.handle.net/10356/82159
http://hdl.handle.net/10220/41101
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