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Production of human pro-relaxin H2 in the yeast Pichia pastoris

BACKGROUND: Initially known as the reproductive hormone, relaxin was shown to possess other therapeutically useful properties that include extracellular matrix remodeling, anti-inflammatory, anti-ischemic and angiogenic effects. All these findings make relaxin a potential drug for diverse medical ap...

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Autores principales: Cimini, D., Corte, K. Della, Finamore, R., Andreozzi, L., Stellavato, A., Pirozzi, A. V. A., Ferrara, F., Formisano, R., De Rosa, M., Chino, M., Lista, L., Lombardi, A., Pavone, V., Schiraldi, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237503/
https://www.ncbi.nlm.nih.gov/pubmed/28088197
http://dx.doi.org/10.1186/s12896-016-0319-0
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author Cimini, D.
Corte, K. Della
Finamore, R.
Andreozzi, L.
Stellavato, A.
Pirozzi, A. V. A.
Ferrara, F.
Formisano, R.
De Rosa, M.
Chino, M.
Lista, L.
Lombardi, A.
Pavone, V.
Schiraldi, C.
author_facet Cimini, D.
Corte, K. Della
Finamore, R.
Andreozzi, L.
Stellavato, A.
Pirozzi, A. V. A.
Ferrara, F.
Formisano, R.
De Rosa, M.
Chino, M.
Lista, L.
Lombardi, A.
Pavone, V.
Schiraldi, C.
author_sort Cimini, D.
collection PubMed
description BACKGROUND: Initially known as the reproductive hormone, relaxin was shown to possess other therapeutically useful properties that include extracellular matrix remodeling, anti-inflammatory, anti-ischemic and angiogenic effects. All these findings make relaxin a potential drug for diverse medical applications. Its precursor, pro-relaxin, is an 18 kDa protein, that shows activity in in vitro assays. Since extraction of relaxin from animal tissues raises several issues, prokaryotes and eukaryotes were both used as expression systems for recombinant relaxin production. Most productive results were obtained when using Escherichia coli as a host for human relaxin expression. However, in such host, relaxin precipitated in the form of inclusion bodies and, therefore, required several expensive recovery steps as cell lysis, refolding and reduction. RESULTS: To overcome the issues related to prokaryotic expression here we report the production and purification of secreted human pro-relaxin H2 by using the methylotrophic yeast Pichia pastoris as expression host. The methanol inducible promoter AOX1 was used to drive expression of the native and histidine tagged forms of pro-relaxin H2 in dual phase fed-batch experiments on the 22 L scale. Both protein forms presented the correct structure, as determined by mass spectrometry and western blotting analyses, and demonstrated to be biologically active in immune enzymatic assays. The presence of the tag allowed to simplify pro-relaxin purification obtaining higher purity. CONCLUSIONS: This work presents a strategy for microbial production of recombinant human pro-relaxin H2 in Pichia pastoris that allowed the obtainment of biologically active pro-hormone, with a final concentration in the fermentation broth ranging between 10 and 14 mg/L of product, as determined by densitometric analyses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-016-0319-0) contains supplementary material, which is available to authorized users.
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spelling pubmed-52375032017-01-18 Production of human pro-relaxin H2 in the yeast Pichia pastoris Cimini, D. Corte, K. Della Finamore, R. Andreozzi, L. Stellavato, A. Pirozzi, A. V. A. Ferrara, F. Formisano, R. De Rosa, M. Chino, M. Lista, L. Lombardi, A. Pavone, V. Schiraldi, C. BMC Biotechnol Research Article BACKGROUND: Initially known as the reproductive hormone, relaxin was shown to possess other therapeutically useful properties that include extracellular matrix remodeling, anti-inflammatory, anti-ischemic and angiogenic effects. All these findings make relaxin a potential drug for diverse medical applications. Its precursor, pro-relaxin, is an 18 kDa protein, that shows activity in in vitro assays. Since extraction of relaxin from animal tissues raises several issues, prokaryotes and eukaryotes were both used as expression systems for recombinant relaxin production. Most productive results were obtained when using Escherichia coli as a host for human relaxin expression. However, in such host, relaxin precipitated in the form of inclusion bodies and, therefore, required several expensive recovery steps as cell lysis, refolding and reduction. RESULTS: To overcome the issues related to prokaryotic expression here we report the production and purification of secreted human pro-relaxin H2 by using the methylotrophic yeast Pichia pastoris as expression host. The methanol inducible promoter AOX1 was used to drive expression of the native and histidine tagged forms of pro-relaxin H2 in dual phase fed-batch experiments on the 22 L scale. Both protein forms presented the correct structure, as determined by mass spectrometry and western blotting analyses, and demonstrated to be biologically active in immune enzymatic assays. The presence of the tag allowed to simplify pro-relaxin purification obtaining higher purity. CONCLUSIONS: This work presents a strategy for microbial production of recombinant human pro-relaxin H2 in Pichia pastoris that allowed the obtainment of biologically active pro-hormone, with a final concentration in the fermentation broth ranging between 10 and 14 mg/L of product, as determined by densitometric analyses. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12896-016-0319-0) contains supplementary material, which is available to authorized users. BioMed Central 2017-01-14 /pmc/articles/PMC5237503/ /pubmed/28088197 http://dx.doi.org/10.1186/s12896-016-0319-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Cimini, D.
Corte, K. Della
Finamore, R.
Andreozzi, L.
Stellavato, A.
Pirozzi, A. V. A.
Ferrara, F.
Formisano, R.
De Rosa, M.
Chino, M.
Lista, L.
Lombardi, A.
Pavone, V.
Schiraldi, C.
Production of human pro-relaxin H2 in the yeast Pichia pastoris
title Production of human pro-relaxin H2 in the yeast Pichia pastoris
title_full Production of human pro-relaxin H2 in the yeast Pichia pastoris
title_fullStr Production of human pro-relaxin H2 in the yeast Pichia pastoris
title_full_unstemmed Production of human pro-relaxin H2 in the yeast Pichia pastoris
title_short Production of human pro-relaxin H2 in the yeast Pichia pastoris
title_sort production of human pro-relaxin h2 in the yeast pichia pastoris
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237503/
https://www.ncbi.nlm.nih.gov/pubmed/28088197
http://dx.doi.org/10.1186/s12896-016-0319-0
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