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Cloning and expression of an anti-cancerous cytokine: human IL-29 gene in Chlamydomonas reinhardtii
Green algae, Chlamydomonas reinhardtii, with low cultivation cost, absence of endotoxins and insusceptibility to human pathogens is emerging as a potential system for the future production of recombinant proteins. The recent development of molecular tools enabling recombinant protein expression in a...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968364/ https://www.ncbi.nlm.nih.gov/pubmed/36840830 http://dx.doi.org/10.1186/s13568-023-01530-1 |
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author | Akram, Maham Khan, Mohsin Ahmad Ahmed, Nadeem Bhatti, Rashid Pervaiz, Rabbia Malik, Kausar Tahir, Saad Abbas, Rabia Ashraf, Fareeha Ali, Qurban |
author_facet | Akram, Maham Khan, Mohsin Ahmad Ahmed, Nadeem Bhatti, Rashid Pervaiz, Rabbia Malik, Kausar Tahir, Saad Abbas, Rabia Ashraf, Fareeha Ali, Qurban |
author_sort | Akram, Maham |
collection | PubMed |
description | Green algae, Chlamydomonas reinhardtii, with low cultivation cost, absence of endotoxins and insusceptibility to human pathogens is emerging as a potential system for the future production of recombinant proteins. The recent development of molecular tools enabling recombinant protein expression in algae chloroplast has provided new research and advance opportunities for developing low-cost therapeutic proteins. In the present study, algae chloroplast expression system was evaluated for the recombinant production of an anti-cancerous therapeutic protein, Interleukin 29 (IL29). The IL29 gene was cloned into algae chloroplast expression vector (pSRSapI). After the transformation, the positive clones were screened for homoplasmy and the presence of the IL29 gene by spot test and PCR analysis, respectively. The expressed SDS-PAGE and western blotting assay characterized IL-29. The algae expressed IL-29 was biologically active in an anti-proliferating bioassay using HepG2 cells. The results suggest that the Chlamydomonas reinhardtii expression system is convenient, low-cost, eco-friendly, and safe to express IL29. |
format | Online Article Text |
id | pubmed-9968364 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-99683642023-02-27 Cloning and expression of an anti-cancerous cytokine: human IL-29 gene in Chlamydomonas reinhardtii Akram, Maham Khan, Mohsin Ahmad Ahmed, Nadeem Bhatti, Rashid Pervaiz, Rabbia Malik, Kausar Tahir, Saad Abbas, Rabia Ashraf, Fareeha Ali, Qurban AMB Express Original Article Green algae, Chlamydomonas reinhardtii, with low cultivation cost, absence of endotoxins and insusceptibility to human pathogens is emerging as a potential system for the future production of recombinant proteins. The recent development of molecular tools enabling recombinant protein expression in algae chloroplast has provided new research and advance opportunities for developing low-cost therapeutic proteins. In the present study, algae chloroplast expression system was evaluated for the recombinant production of an anti-cancerous therapeutic protein, Interleukin 29 (IL29). The IL29 gene was cloned into algae chloroplast expression vector (pSRSapI). After the transformation, the positive clones were screened for homoplasmy and the presence of the IL29 gene by spot test and PCR analysis, respectively. The expressed SDS-PAGE and western blotting assay characterized IL-29. The algae expressed IL-29 was biologically active in an anti-proliferating bioassay using HepG2 cells. The results suggest that the Chlamydomonas reinhardtii expression system is convenient, low-cost, eco-friendly, and safe to express IL29. Springer Berlin Heidelberg 2023-02-25 /pmc/articles/PMC9968364/ /pubmed/36840830 http://dx.doi.org/10.1186/s13568-023-01530-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Akram, Maham Khan, Mohsin Ahmad Ahmed, Nadeem Bhatti, Rashid Pervaiz, Rabbia Malik, Kausar Tahir, Saad Abbas, Rabia Ashraf, Fareeha Ali, Qurban Cloning and expression of an anti-cancerous cytokine: human IL-29 gene in Chlamydomonas reinhardtii |
title | Cloning and expression of an anti-cancerous cytokine: human IL-29 gene in Chlamydomonas reinhardtii |
title_full | Cloning and expression of an anti-cancerous cytokine: human IL-29 gene in Chlamydomonas reinhardtii |
title_fullStr | Cloning and expression of an anti-cancerous cytokine: human IL-29 gene in Chlamydomonas reinhardtii |
title_full_unstemmed | Cloning and expression of an anti-cancerous cytokine: human IL-29 gene in Chlamydomonas reinhardtii |
title_short | Cloning and expression of an anti-cancerous cytokine: human IL-29 gene in Chlamydomonas reinhardtii |
title_sort | cloning and expression of an anti-cancerous cytokine: human il-29 gene in chlamydomonas reinhardtii |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9968364/ https://www.ncbi.nlm.nih.gov/pubmed/36840830 http://dx.doi.org/10.1186/s13568-023-01530-1 |
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