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An improved secretion signal enhances the secretion of model proteins from Pichia pastoris
BACKGROUND: Proteins can be secreted from a host organism with the aid of N-terminal secretion signals. The budding yeast Pichia pastoris (Komagataella sp.) is widely employed to secrete proteins of academic and industrial interest. For this yeast, the most commonly used secretion signal is the N-te...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182871/ https://www.ncbi.nlm.nih.gov/pubmed/30314480 http://dx.doi.org/10.1186/s12934-018-1009-5 |
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author | Barrero, Juan J. Casler, Jason C. Valero, Francisco Ferrer, Pau Glick, Benjamin S. |
author_facet | Barrero, Juan J. Casler, Jason C. Valero, Francisco Ferrer, Pau Glick, Benjamin S. |
author_sort | Barrero, Juan J. |
collection | PubMed |
description | BACKGROUND: Proteins can be secreted from a host organism with the aid of N-terminal secretion signals. The budding yeast Pichia pastoris (Komagataella sp.) is widely employed to secrete proteins of academic and industrial interest. For this yeast, the most commonly used secretion signal is the N-terminal portion of pre-pro-α-factor from Saccharomyces cerevisiae. However, this secretion signal promotes posttranslational translocation into the endoplasmic reticulum (ER), so proteins that can fold in the cytosol may be inefficiently translocated and thus poorly secreted. In addition, if a protein self-associates, the α-factor pro region can potentially cause aggregation, thereby hampering export from the ER. This study addresses both limitations of the pre-pro-α-factor secretion signal. RESULTS: We engineered a hybrid secretion signal consisting of the S. cerevisiae Ost1 signal sequence, which promotes cotranslational translocation into the ER, followed by the α-factor pro region. Secretion and intracellular localization were assessed using as a model protein the tetrameric red fluorescent protein E2-Crimson. When paired with the α-factor pro region, the Ost1 signal sequence yielded much more efficient secretion than the α-factor signal sequence. Moreover, an allelic variant of the α-factor pro region reduced aggregation of the E2-Crimson construct in the ER. The resulting improved secretion signal enhanced secretion of E2-Crimson up to 20-fold compared to the levels obtained with the original α-factor secretion signal. Similar findings were obtained with the lipase BTL2, which exhibited 10-fold enhanced secretion with the improved secretion signal. CONCLUSIONS: The improved secretion signal confers dramatic benefits for the secretion of certain proteins from P. pastoris. These benefits are likely to be most evident for proteins that can fold in the cytosol and for oligomeric proteins. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-1009-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6182871 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61828712018-10-18 An improved secretion signal enhances the secretion of model proteins from Pichia pastoris Barrero, Juan J. Casler, Jason C. Valero, Francisco Ferrer, Pau Glick, Benjamin S. Microb Cell Fact Research BACKGROUND: Proteins can be secreted from a host organism with the aid of N-terminal secretion signals. The budding yeast Pichia pastoris (Komagataella sp.) is widely employed to secrete proteins of academic and industrial interest. For this yeast, the most commonly used secretion signal is the N-terminal portion of pre-pro-α-factor from Saccharomyces cerevisiae. However, this secretion signal promotes posttranslational translocation into the endoplasmic reticulum (ER), so proteins that can fold in the cytosol may be inefficiently translocated and thus poorly secreted. In addition, if a protein self-associates, the α-factor pro region can potentially cause aggregation, thereby hampering export from the ER. This study addresses both limitations of the pre-pro-α-factor secretion signal. RESULTS: We engineered a hybrid secretion signal consisting of the S. cerevisiae Ost1 signal sequence, which promotes cotranslational translocation into the ER, followed by the α-factor pro region. Secretion and intracellular localization were assessed using as a model protein the tetrameric red fluorescent protein E2-Crimson. When paired with the α-factor pro region, the Ost1 signal sequence yielded much more efficient secretion than the α-factor signal sequence. Moreover, an allelic variant of the α-factor pro region reduced aggregation of the E2-Crimson construct in the ER. The resulting improved secretion signal enhanced secretion of E2-Crimson up to 20-fold compared to the levels obtained with the original α-factor secretion signal. Similar findings were obtained with the lipase BTL2, which exhibited 10-fold enhanced secretion with the improved secretion signal. CONCLUSIONS: The improved secretion signal confers dramatic benefits for the secretion of certain proteins from P. pastoris. These benefits are likely to be most evident for proteins that can fold in the cytosol and for oligomeric proteins. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12934-018-1009-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-12 /pmc/articles/PMC6182871/ /pubmed/30314480 http://dx.doi.org/10.1186/s12934-018-1009-5 Text en © The Author(s) 2018 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 Barrero, Juan J. Casler, Jason C. Valero, Francisco Ferrer, Pau Glick, Benjamin S. An improved secretion signal enhances the secretion of model proteins from Pichia pastoris |
title | An improved secretion signal enhances the secretion of model proteins from Pichia pastoris |
title_full | An improved secretion signal enhances the secretion of model proteins from Pichia pastoris |
title_fullStr | An improved secretion signal enhances the secretion of model proteins from Pichia pastoris |
title_full_unstemmed | An improved secretion signal enhances the secretion of model proteins from Pichia pastoris |
title_short | An improved secretion signal enhances the secretion of model proteins from Pichia pastoris |
title_sort | improved secretion signal enhances the secretion of model proteins from pichia pastoris |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182871/ https://www.ncbi.nlm.nih.gov/pubmed/30314480 http://dx.doi.org/10.1186/s12934-018-1009-5 |
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