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Multivalent, Stabilized Mannose‐6‐Phosphates for the Targeted Delivery of Toll‐Like Receptor Ligands and Peptide Antigens
Mannose‐6‐phosphate (M6P) is recognized by the mannose‐6‐phosphate receptor and plays an important role in the transport of cargo to the endosomes, making it an attractive tool to improve endosomal trafficking of vaccines. We describe herein the assembly of peptide antigen conjugates carrying cluste...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894537/ https://www.ncbi.nlm.nih.gov/pubmed/32864819 http://dx.doi.org/10.1002/cbic.202000538 |
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author | Reintjens, Niels R. M. Tondini, Elena Vis, Christopher McGlinn, Toroa Meeuwenoord, Nico J. Hogervorst, Tim P. Overkleeft, Herman S. Filippov, Dmitri V. van der Marel, Gijsbert A. Ossendorp, Ferry Codée, Jeroen D. C. |
author_facet | Reintjens, Niels R. M. Tondini, Elena Vis, Christopher McGlinn, Toroa Meeuwenoord, Nico J. Hogervorst, Tim P. Overkleeft, Herman S. Filippov, Dmitri V. van der Marel, Gijsbert A. Ossendorp, Ferry Codée, Jeroen D. C. |
author_sort | Reintjens, Niels R. M. |
collection | PubMed |
description | Mannose‐6‐phosphate (M6P) is recognized by the mannose‐6‐phosphate receptor and plays an important role in the transport of cargo to the endosomes, making it an attractive tool to improve endosomal trafficking of vaccines. We describe herein the assembly of peptide antigen conjugates carrying clusters of mannose‐6‐C‐phosphonates (M6Po). The M6Po's are stable M6P mimics that are resistant to cleavage of the phosphate group by endogenous phosphatases. Two different strategies for the incorporation of the M6Po clusters in the conjugate have been developed: the first relies on a “post‐assembly” click approach employing an M6Po bearing an alkyne functionality; the second hinges on an M6Po C‐glycoside amino acid building block that can be used in solid‐phase peptide synthesis. The generated conjugates were further equipped with a TLR7 ligand to stimulate dendritic cell (DC) maturation. While antigen presentation is hindered by the presence of the M6Po clusters, the incorporation of the M6Po clusters leads to increased activation of DCs, thus demonstrating their potential in improving vaccine adjuvanticity by intraendosomally active TLR ligands. |
format | Online Article Text |
id | pubmed-7894537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78945372021-03-02 Multivalent, Stabilized Mannose‐6‐Phosphates for the Targeted Delivery of Toll‐Like Receptor Ligands and Peptide Antigens Reintjens, Niels R. M. Tondini, Elena Vis, Christopher McGlinn, Toroa Meeuwenoord, Nico J. Hogervorst, Tim P. Overkleeft, Herman S. Filippov, Dmitri V. van der Marel, Gijsbert A. Ossendorp, Ferry Codée, Jeroen D. C. Chembiochem Full Papers Mannose‐6‐phosphate (M6P) is recognized by the mannose‐6‐phosphate receptor and plays an important role in the transport of cargo to the endosomes, making it an attractive tool to improve endosomal trafficking of vaccines. We describe herein the assembly of peptide antigen conjugates carrying clusters of mannose‐6‐C‐phosphonates (M6Po). The M6Po's are stable M6P mimics that are resistant to cleavage of the phosphate group by endogenous phosphatases. Two different strategies for the incorporation of the M6Po clusters in the conjugate have been developed: the first relies on a “post‐assembly” click approach employing an M6Po bearing an alkyne functionality; the second hinges on an M6Po C‐glycoside amino acid building block that can be used in solid‐phase peptide synthesis. The generated conjugates were further equipped with a TLR7 ligand to stimulate dendritic cell (DC) maturation. While antigen presentation is hindered by the presence of the M6Po clusters, the incorporation of the M6Po clusters leads to increased activation of DCs, thus demonstrating their potential in improving vaccine adjuvanticity by intraendosomally active TLR ligands. John Wiley and Sons Inc. 2020-10-23 2021-01-15 /pmc/articles/PMC7894537/ /pubmed/32864819 http://dx.doi.org/10.1002/cbic.202000538 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Reintjens, Niels R. M. Tondini, Elena Vis, Christopher McGlinn, Toroa Meeuwenoord, Nico J. Hogervorst, Tim P. Overkleeft, Herman S. Filippov, Dmitri V. van der Marel, Gijsbert A. Ossendorp, Ferry Codée, Jeroen D. C. Multivalent, Stabilized Mannose‐6‐Phosphates for the Targeted Delivery of Toll‐Like Receptor Ligands and Peptide Antigens |
title | Multivalent, Stabilized Mannose‐6‐Phosphates for the Targeted Delivery of Toll‐Like Receptor Ligands and Peptide Antigens |
title_full | Multivalent, Stabilized Mannose‐6‐Phosphates for the Targeted Delivery of Toll‐Like Receptor Ligands and Peptide Antigens |
title_fullStr | Multivalent, Stabilized Mannose‐6‐Phosphates for the Targeted Delivery of Toll‐Like Receptor Ligands and Peptide Antigens |
title_full_unstemmed | Multivalent, Stabilized Mannose‐6‐Phosphates for the Targeted Delivery of Toll‐Like Receptor Ligands and Peptide Antigens |
title_short | Multivalent, Stabilized Mannose‐6‐Phosphates for the Targeted Delivery of Toll‐Like Receptor Ligands and Peptide Antigens |
title_sort | multivalent, stabilized mannose‐6‐phosphates for the targeted delivery of toll‐like receptor ligands and peptide antigens |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7894537/ https://www.ncbi.nlm.nih.gov/pubmed/32864819 http://dx.doi.org/10.1002/cbic.202000538 |
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