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Hybrid Nanomaterial Complexes for Advanced Phage-guided Gene Delivery
Developing nanomaterials that are effective, safe, and selective for gene transfer applications is challenging. Bacteriophages (phage), viruses that infect bacteria only, have shown promise for targeted gene transfer applications. Unfortunately, limited progress has been achieved in improving their...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221597/ https://www.ncbi.nlm.nih.gov/pubmed/25118171 http://dx.doi.org/10.1038/mtna.2014.37 |
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author | Yata, Teerapong Lee, Koon-Yang Dharakul, Tararaj Songsivilai, Sirirurg Bismarck, Alexander Mintz, Paul J Hajitou, Amin |
author_facet | Yata, Teerapong Lee, Koon-Yang Dharakul, Tararaj Songsivilai, Sirirurg Bismarck, Alexander Mintz, Paul J Hajitou, Amin |
author_sort | Yata, Teerapong |
collection | PubMed |
description | Developing nanomaterials that are effective, safe, and selective for gene transfer applications is challenging. Bacteriophages (phage), viruses that infect bacteria only, have shown promise for targeted gene transfer applications. Unfortunately, limited progress has been achieved in improving their potential to overcome mammalian cellular barriers. We hypothesized that chemical modification of the bacteriophage capsid could be applied to improve targeted gene delivery by phage vectors into mammalian cells. Here, we introduce a novel hybrid system consisting of two classes of nanomaterial systems, cationic polymers and M13 bacteriophage virus particles genetically engineered to display a tumor-targeting ligand and carry a transgene cassette. We demonstrate that the phage complex with cationic polymers generates positively charged phage and large aggregates that show enhanced cell surface attachment, buffering capacity, and improved transgene expression while retaining cell type specificity. Moreover, phage/polymer complexes carrying a therapeutic gene achieve greater cancer cell killing than phage alone. This new class of hybrid nanomaterial platform can advance targeted gene delivery applications by bacteriophage. |
format | Online Article Text |
id | pubmed-4221597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-42215972014-11-13 Hybrid Nanomaterial Complexes for Advanced Phage-guided Gene Delivery Yata, Teerapong Lee, Koon-Yang Dharakul, Tararaj Songsivilai, Sirirurg Bismarck, Alexander Mintz, Paul J Hajitou, Amin Mol Ther Nucleic Acids Original Article Developing nanomaterials that are effective, safe, and selective for gene transfer applications is challenging. Bacteriophages (phage), viruses that infect bacteria only, have shown promise for targeted gene transfer applications. Unfortunately, limited progress has been achieved in improving their potential to overcome mammalian cellular barriers. We hypothesized that chemical modification of the bacteriophage capsid could be applied to improve targeted gene delivery by phage vectors into mammalian cells. Here, we introduce a novel hybrid system consisting of two classes of nanomaterial systems, cationic polymers and M13 bacteriophage virus particles genetically engineered to display a tumor-targeting ligand and carry a transgene cassette. We demonstrate that the phage complex with cationic polymers generates positively charged phage and large aggregates that show enhanced cell surface attachment, buffering capacity, and improved transgene expression while retaining cell type specificity. Moreover, phage/polymer complexes carrying a therapeutic gene achieve greater cancer cell killing than phage alone. This new class of hybrid nanomaterial platform can advance targeted gene delivery applications by bacteriophage. Nature Publishing Group 2014-08 2014-08-12 /pmc/articles/PMC4221597/ /pubmed/25118171 http://dx.doi.org/10.1038/mtna.2014.37 Text en Copyright © 2014 American Society of Gene & Cell Therapy http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Original Article Yata, Teerapong Lee, Koon-Yang Dharakul, Tararaj Songsivilai, Sirirurg Bismarck, Alexander Mintz, Paul J Hajitou, Amin Hybrid Nanomaterial Complexes for Advanced Phage-guided Gene Delivery |
title | Hybrid Nanomaterial Complexes for Advanced Phage-guided Gene Delivery |
title_full | Hybrid Nanomaterial Complexes for Advanced Phage-guided Gene Delivery |
title_fullStr | Hybrid Nanomaterial Complexes for Advanced Phage-guided Gene Delivery |
title_full_unstemmed | Hybrid Nanomaterial Complexes for Advanced Phage-guided Gene Delivery |
title_short | Hybrid Nanomaterial Complexes for Advanced Phage-guided Gene Delivery |
title_sort | hybrid nanomaterial complexes for advanced phage-guided gene delivery |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221597/ https://www.ncbi.nlm.nih.gov/pubmed/25118171 http://dx.doi.org/10.1038/mtna.2014.37 |
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