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‘Multicopy Multivalent’ Glycopolymer-Stabilized Gold Nanoparticles as Potential Synthetic Cancer Vaccines
[Image: see text] Mucin-related carbohydrates are overexpressed on the surface of cancer cells, providing a disease-specific target for cancer immunotherapy. Here, we describe the design and construction of peptide-free multivalent glycosylated nanoscale constructs as potential synthetic cancer vacc...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928990/ https://www.ncbi.nlm.nih.gov/pubmed/23763610 http://dx.doi.org/10.1021/ja4046857 |
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author | Parry, Alison L. Clemson, Natasha A. Ellis, James Bernhard, Stefan S. R. Davis, Benjamin G. Cameron, Neil R. |
author_facet | Parry, Alison L. Clemson, Natasha A. Ellis, James Bernhard, Stefan S. R. Davis, Benjamin G. Cameron, Neil R. |
author_sort | Parry, Alison L. |
collection | PubMed |
description | [Image: see text] Mucin-related carbohydrates are overexpressed on the surface of cancer cells, providing a disease-specific target for cancer immunotherapy. Here, we describe the design and construction of peptide-free multivalent glycosylated nanoscale constructs as potential synthetic cancer vaccines that generate significant titers of antibodies selective for aberrant mucin glycans. A polymerizable version of the Tn-antigen glycan was prepared and converted into well-defined glycopolymers by Reversible Addition–Fragmentation chain Transfer (RAFT) polymerization. The polymers were then conjugated to gold nanoparticles, yielding ‘multicopy-multivalent’ nanoscale glycoconjugates. Immunological studies indicated that these nanomaterials generated strong and long-lasting production of antibodies that are selective to the Tn-antigen glycan and cross-reactive toward mucin proteins displaying Tn. The results demonstrate proof-of-concept of a simple and modular approach toward synthetic anticancer vaccines based on multivalent glycosylated nanomaterials without the need for a typical vaccine protein component. |
format | Online Article Text |
id | pubmed-3928990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-39289902014-02-19 ‘Multicopy Multivalent’ Glycopolymer-Stabilized Gold Nanoparticles as Potential Synthetic Cancer Vaccines Parry, Alison L. Clemson, Natasha A. Ellis, James Bernhard, Stefan S. R. Davis, Benjamin G. Cameron, Neil R. J Am Chem Soc [Image: see text] Mucin-related carbohydrates are overexpressed on the surface of cancer cells, providing a disease-specific target for cancer immunotherapy. Here, we describe the design and construction of peptide-free multivalent glycosylated nanoscale constructs as potential synthetic cancer vaccines that generate significant titers of antibodies selective for aberrant mucin glycans. A polymerizable version of the Tn-antigen glycan was prepared and converted into well-defined glycopolymers by Reversible Addition–Fragmentation chain Transfer (RAFT) polymerization. The polymers were then conjugated to gold nanoparticles, yielding ‘multicopy-multivalent’ nanoscale glycoconjugates. Immunological studies indicated that these nanomaterials generated strong and long-lasting production of antibodies that are selective to the Tn-antigen glycan and cross-reactive toward mucin proteins displaying Tn. The results demonstrate proof-of-concept of a simple and modular approach toward synthetic anticancer vaccines based on multivalent glycosylated nanomaterials without the need for a typical vaccine protein component. American Chemical Society 2013-06-13 2013-06-26 /pmc/articles/PMC3928990/ /pubmed/23763610 http://dx.doi.org/10.1021/ja4046857 Text en Copyright © 2013 American Chemical Society Terms of Use CC-BY (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) |
spellingShingle | Parry, Alison L. Clemson, Natasha A. Ellis, James Bernhard, Stefan S. R. Davis, Benjamin G. Cameron, Neil R. ‘Multicopy Multivalent’ Glycopolymer-Stabilized Gold Nanoparticles as Potential Synthetic Cancer Vaccines |
title | ‘Multicopy Multivalent’ Glycopolymer-Stabilized
Gold Nanoparticles as Potential Synthetic Cancer Vaccines |
title_full | ‘Multicopy Multivalent’ Glycopolymer-Stabilized
Gold Nanoparticles as Potential Synthetic Cancer Vaccines |
title_fullStr | ‘Multicopy Multivalent’ Glycopolymer-Stabilized
Gold Nanoparticles as Potential Synthetic Cancer Vaccines |
title_full_unstemmed | ‘Multicopy Multivalent’ Glycopolymer-Stabilized
Gold Nanoparticles as Potential Synthetic Cancer Vaccines |
title_short | ‘Multicopy Multivalent’ Glycopolymer-Stabilized
Gold Nanoparticles as Potential Synthetic Cancer Vaccines |
title_sort | ‘multicopy multivalent’ glycopolymer-stabilized
gold nanoparticles as potential synthetic cancer vaccines |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3928990/ https://www.ncbi.nlm.nih.gov/pubmed/23763610 http://dx.doi.org/10.1021/ja4046857 |
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