Cargando…

‘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...

Descripción completa

Detalles Bibliográficos
Autores principales: Parry, Alison L., Clemson, Natasha A., Ellis, James, Bernhard, Stefan S. R., Davis, Benjamin G., Cameron, Neil R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2013
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
_version_ 1782304337378148352
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
work_keys_str_mv AT parryalisonl multicopymultivalentglycopolymerstabilizedgoldnanoparticlesaspotentialsyntheticcancervaccines
AT clemsonnatashaa multicopymultivalentglycopolymerstabilizedgoldnanoparticlesaspotentialsyntheticcancervaccines
AT ellisjames multicopymultivalentglycopolymerstabilizedgoldnanoparticlesaspotentialsyntheticcancervaccines
AT bernhardstefansr multicopymultivalentglycopolymerstabilizedgoldnanoparticlesaspotentialsyntheticcancervaccines
AT davisbenjaming multicopymultivalentglycopolymerstabilizedgoldnanoparticlesaspotentialsyntheticcancervaccines
AT cameronneilr multicopymultivalentglycopolymerstabilizedgoldnanoparticlesaspotentialsyntheticcancervaccines