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Cell-specific targeting by engineered M13 bacteriophage expressing VEGFR2 nanobody
OBJECTIVE(S): Filamentous bacteriophage M13 was genetically engineered to specifically target mammalian cells for gene delivery purpose. MATERIALS AND METHODS: A vascular endothelial growth factor receptor 2 (VEGFR2)-specific nanobody was genetically fused to the capsid gene III of M13 bacteriophage...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mashhad University of Medical Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272075/ https://www.ncbi.nlm.nih.gov/pubmed/30524687 http://dx.doi.org/10.22038/IJBMS.2018.26191.6432 |
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author | Ranjibar, Farideh Habibi-Anbouhi, Mahdi Kazemi-Lomedasht, Fatemeh Aghaee-Bakhtiyari, Seyed Hamid Alirahimi, Ehsan Behdani, Mahdi |
author_facet | Ranjibar, Farideh Habibi-Anbouhi, Mahdi Kazemi-Lomedasht, Fatemeh Aghaee-Bakhtiyari, Seyed Hamid Alirahimi, Ehsan Behdani, Mahdi |
author_sort | Ranjibar, Farideh |
collection | PubMed |
description | OBJECTIVE(S): Filamentous bacteriophage M13 was genetically engineered to specifically target mammalian cells for gene delivery purpose. MATERIALS AND METHODS: A vascular endothelial growth factor receptor 2 (VEGFR2)-specific nanobody was genetically fused to the capsid gene III of M13 bacteriophage (pHEN4/3VGR19). A mammalian expression construct containing Cop-green fluorescent protein (Cop-GFP), as a reporter gene, was amplified by PCR and then sub-cloned in the pHEN4/3VGR19 phagemid. The resulting construct was transfected into 293KDR cell. The recombinant phage was extracted and confirmed and then transduced into VEGFR2 expressing cell (293KDR). RESULTS: Seventy-two hr after transfection, green fluorescence was detected in 30% of the cells. About 1% of the cells which transduced by recombinant phages were able to express GFP. CONCLUSION: It is hoped that the results from this study will help to find potential vectors to improve the efficiency of gene delivery. Taken together, we conclude that this newly-introduced vector can be used in cancer researches. |
format | Online Article Text |
id | pubmed-6272075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-62720752018-12-06 Cell-specific targeting by engineered M13 bacteriophage expressing VEGFR2 nanobody Ranjibar, Farideh Habibi-Anbouhi, Mahdi Kazemi-Lomedasht, Fatemeh Aghaee-Bakhtiyari, Seyed Hamid Alirahimi, Ehsan Behdani, Mahdi Iran J Basic Med Sci Original Article OBJECTIVE(S): Filamentous bacteriophage M13 was genetically engineered to specifically target mammalian cells for gene delivery purpose. MATERIALS AND METHODS: A vascular endothelial growth factor receptor 2 (VEGFR2)-specific nanobody was genetically fused to the capsid gene III of M13 bacteriophage (pHEN4/3VGR19). A mammalian expression construct containing Cop-green fluorescent protein (Cop-GFP), as a reporter gene, was amplified by PCR and then sub-cloned in the pHEN4/3VGR19 phagemid. The resulting construct was transfected into 293KDR cell. The recombinant phage was extracted and confirmed and then transduced into VEGFR2 expressing cell (293KDR). RESULTS: Seventy-two hr after transfection, green fluorescence was detected in 30% of the cells. About 1% of the cells which transduced by recombinant phages were able to express GFP. CONCLUSION: It is hoped that the results from this study will help to find potential vectors to improve the efficiency of gene delivery. Taken together, we conclude that this newly-introduced vector can be used in cancer researches. Mashhad University of Medical Sciences 2018-09 /pmc/articles/PMC6272075/ /pubmed/30524687 http://dx.doi.org/10.22038/IJBMS.2018.26191.6432 Text en This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Ranjibar, Farideh Habibi-Anbouhi, Mahdi Kazemi-Lomedasht, Fatemeh Aghaee-Bakhtiyari, Seyed Hamid Alirahimi, Ehsan Behdani, Mahdi Cell-specific targeting by engineered M13 bacteriophage expressing VEGFR2 nanobody |
title | Cell-specific targeting by engineered M13 bacteriophage expressing VEGFR2 nanobody |
title_full | Cell-specific targeting by engineered M13 bacteriophage expressing VEGFR2 nanobody |
title_fullStr | Cell-specific targeting by engineered M13 bacteriophage expressing VEGFR2 nanobody |
title_full_unstemmed | Cell-specific targeting by engineered M13 bacteriophage expressing VEGFR2 nanobody |
title_short | Cell-specific targeting by engineered M13 bacteriophage expressing VEGFR2 nanobody |
title_sort | cell-specific targeting by engineered m13 bacteriophage expressing vegfr2 nanobody |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272075/ https://www.ncbi.nlm.nih.gov/pubmed/30524687 http://dx.doi.org/10.22038/IJBMS.2018.26191.6432 |
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