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Transient expression of CCL21as recombinant protein in tomato

The main goal of this study was to investigate the possibility of expressing recombinant protein of C-C chemokine ligand 21 (CCL21) in Solanum lycopersicum via agroinfiltration. CCL21 is a chemokine can be used for anti-metastatic of cancer cell lines. To examine the expression of CCL21 protein in S...

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Detalles Bibliográficos
Autores principales: Beihaghi, Maria, Marashi, Hasan, Bagheri, Abdolreza, Sankian, Mojtaba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730375/
https://www.ncbi.nlm.nih.gov/pubmed/29276695
http://dx.doi.org/10.1016/j.btre.2017.11.007
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author Beihaghi, Maria
Marashi, Hasan
Bagheri, Abdolreza
Sankian, Mojtaba
author_facet Beihaghi, Maria
Marashi, Hasan
Bagheri, Abdolreza
Sankian, Mojtaba
author_sort Beihaghi, Maria
collection PubMed
description The main goal of this study was to investigate the possibility of expressing recombinant protein of C-C chemokine ligand 21 (CCL21) in Solanum lycopersicum via agroinfiltration. CCL21 is a chemokine can be used for anti-metastatic of cancer cell lines. To examine the expression of CCL21 protein in S. lycopersicum, the construct of ccl21 was synthesized. This construct was cloned into pBI121 and the resulting CCL21 plasmid was agro-infiltrated into S. lycopersicum leaves. Within three days after infiltration, Expression of the foreign gene was confirmed by quantitative Real-time PCR. A recombinant CCL21 protein was immunogenically detected by western blot, dot blot and ELISA assay. And results showed that the foreign gene was expressed in the transformed leaves in high level. Also scratch assay was used to investigate the role of this protein in anti-metastatic function. The results demonstrated anti-metastatic of cancer cells in the presence of this protein.
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spelling pubmed-57303752017-12-22 Transient expression of CCL21as recombinant protein in tomato Beihaghi, Maria Marashi, Hasan Bagheri, Abdolreza Sankian, Mojtaba Biotechnol Rep (Amst) Article The main goal of this study was to investigate the possibility of expressing recombinant protein of C-C chemokine ligand 21 (CCL21) in Solanum lycopersicum via agroinfiltration. CCL21 is a chemokine can be used for anti-metastatic of cancer cell lines. To examine the expression of CCL21 protein in S. lycopersicum, the construct of ccl21 was synthesized. This construct was cloned into pBI121 and the resulting CCL21 plasmid was agro-infiltrated into S. lycopersicum leaves. Within three days after infiltration, Expression of the foreign gene was confirmed by quantitative Real-time PCR. A recombinant CCL21 protein was immunogenically detected by western blot, dot blot and ELISA assay. And results showed that the foreign gene was expressed in the transformed leaves in high level. Also scratch assay was used to investigate the role of this protein in anti-metastatic function. The results demonstrated anti-metastatic of cancer cells in the presence of this protein. Elsevier 2017-11-26 /pmc/articles/PMC5730375/ /pubmed/29276695 http://dx.doi.org/10.1016/j.btre.2017.11.007 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Beihaghi, Maria
Marashi, Hasan
Bagheri, Abdolreza
Sankian, Mojtaba
Transient expression of CCL21as recombinant protein in tomato
title Transient expression of CCL21as recombinant protein in tomato
title_full Transient expression of CCL21as recombinant protein in tomato
title_fullStr Transient expression of CCL21as recombinant protein in tomato
title_full_unstemmed Transient expression of CCL21as recombinant protein in tomato
title_short Transient expression of CCL21as recombinant protein in tomato
title_sort transient expression of ccl21as recombinant protein in tomato
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5730375/
https://www.ncbi.nlm.nih.gov/pubmed/29276695
http://dx.doi.org/10.1016/j.btre.2017.11.007
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