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Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli
BACKGROUND: Neurotrophic factors influence survival, differentiation, proliferation and death of neuronal cells within the central nervous system. Human ciliary neurotrophic factor (hCNTF) has neuroprotective properties and is also known to influence energy balance. Consequently, hCNTF has potential...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237735/ https://www.ncbi.nlm.nih.gov/pubmed/25394427 http://dx.doi.org/10.1186/s12896-014-0092-x |
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author | Itkonen, Jaakko M Urtti, Arto Bird, Louise E Sarkhel, Sanjay |
author_facet | Itkonen, Jaakko M Urtti, Arto Bird, Louise E Sarkhel, Sanjay |
author_sort | Itkonen, Jaakko M |
collection | PubMed |
description | BACKGROUND: Neurotrophic factors influence survival, differentiation, proliferation and death of neuronal cells within the central nervous system. Human ciliary neurotrophic factor (hCNTF) has neuroprotective properties and is also known to influence energy balance. Consequently, hCNTF has potential therapeutic applications in neurodegenerative, obesity and diabetes related disorders. Clinical and biological applications of hCNTF necessitate a recombinant expression system to produce large amounts of functional protein in soluble form. Earlier attempts to express hCNTF in Escherichia coli (E. coli) were limited by low amounts and the need to refold from inclusion bodies. RESULTS: In this report, we describe a strategy to effectively identify constructs and conditions for soluble expression of hCNTF in E. coli. Small-scale expression screening with soluble fusion tags identified many conditions that yielded soluble expression. Codon optimized 6-His-hCNTF construct showed soluble expression in all the conditions tested. Large-scale culture of the 6-His-hCNTF construct yielded high (10 – 20 fold) soluble expression (8 – 9 fold) as compared to earlier published reports. Functional activity of recombinant 6-His-hCNTF produced was confirmed by its binding to hCNTF receptor (hCNTFRα) with an EC(50) = 36 nM. CONCLUSION: Our results highlight the combination of codon optimization and screening soluble fusion tags as a successful strategy for high yielding soluble expression of hCNTF in E. coli. Codon optimization of the hCNTF sequence seems to be sufficient for soluble expression of hCNTF. The combined approach of codon optimization and soluble fusion tag screen can be an effective strategy for soluble expression of pharmaceutical proteins in E. coli. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-014-0092-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4237735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42377352014-11-21 Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli Itkonen, Jaakko M Urtti, Arto Bird, Louise E Sarkhel, Sanjay BMC Biotechnol Research Article BACKGROUND: Neurotrophic factors influence survival, differentiation, proliferation and death of neuronal cells within the central nervous system. Human ciliary neurotrophic factor (hCNTF) has neuroprotective properties and is also known to influence energy balance. Consequently, hCNTF has potential therapeutic applications in neurodegenerative, obesity and diabetes related disorders. Clinical and biological applications of hCNTF necessitate a recombinant expression system to produce large amounts of functional protein in soluble form. Earlier attempts to express hCNTF in Escherichia coli (E. coli) were limited by low amounts and the need to refold from inclusion bodies. RESULTS: In this report, we describe a strategy to effectively identify constructs and conditions for soluble expression of hCNTF in E. coli. Small-scale expression screening with soluble fusion tags identified many conditions that yielded soluble expression. Codon optimized 6-His-hCNTF construct showed soluble expression in all the conditions tested. Large-scale culture of the 6-His-hCNTF construct yielded high (10 – 20 fold) soluble expression (8 – 9 fold) as compared to earlier published reports. Functional activity of recombinant 6-His-hCNTF produced was confirmed by its binding to hCNTF receptor (hCNTFRα) with an EC(50) = 36 nM. CONCLUSION: Our results highlight the combination of codon optimization and screening soluble fusion tags as a successful strategy for high yielding soluble expression of hCNTF in E. coli. Codon optimization of the hCNTF sequence seems to be sufficient for soluble expression of hCNTF. The combined approach of codon optimization and soluble fusion tag screen can be an effective strategy for soluble expression of pharmaceutical proteins in E. coli. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-014-0092-x) contains supplementary material, which is available to authorized users. BioMed Central 2014-11-14 /pmc/articles/PMC4237735/ /pubmed/25394427 http://dx.doi.org/10.1186/s12896-014-0092-x Text en © Itkonen et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Itkonen, Jaakko M Urtti, Arto Bird, Louise E Sarkhel, Sanjay Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli |
title | Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli |
title_full | Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli |
title_fullStr | Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli |
title_full_unstemmed | Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli |
title_short | Codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in Escherichia coli |
title_sort | codon optimization and factorial screening for enhanced soluble expression of human ciliary neurotrophic factor in escherichia coli |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4237735/ https://www.ncbi.nlm.nih.gov/pubmed/25394427 http://dx.doi.org/10.1186/s12896-014-0092-x |
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