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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...

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Autores principales: Yata, Teerapong, Lee, Koon-Yang, Dharakul, Tararaj, Songsivilai, Sirirurg, Bismarck, Alexander, Mintz, Paul J, Hajitou, Amin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
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.
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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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