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Regioselective Glycosylation Strategies for the Synthesis of Group Ia and Ib Streptococcus Related Glycans Enable Elucidating Unique Conformations of the Capsular Polysaccharides

Group B Streptococcus serotypes Ia and Ib capsular polysaccharides are key targets for vaccine development. In spite of their immunospecifity these polysaccharides share high structural similarity. Both are composed of the same monosaccharide residues and differ only in the connection of the Neu5Acα...

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Autores principales: Del Bino, Linda, Calloni, Ilaria, Oldrini, Davide, Raso, Maria Michelina, Cuffaro, Rossella, Ardá, Ana, Codée, Jeroen D. C., Jiménez‐Barbero, Jesús, Adamo, Roberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972993/
https://www.ncbi.nlm.nih.gov/pubmed/31506992
http://dx.doi.org/10.1002/chem.201903527
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author Del Bino, Linda
Calloni, Ilaria
Oldrini, Davide
Raso, Maria Michelina
Cuffaro, Rossella
Ardá, Ana
Codée, Jeroen D. C.
Jiménez‐Barbero, Jesús
Adamo, Roberto
author_facet Del Bino, Linda
Calloni, Ilaria
Oldrini, Davide
Raso, Maria Michelina
Cuffaro, Rossella
Ardá, Ana
Codée, Jeroen D. C.
Jiménez‐Barbero, Jesús
Adamo, Roberto
author_sort Del Bino, Linda
collection PubMed
description Group B Streptococcus serotypes Ia and Ib capsular polysaccharides are key targets for vaccine development. In spite of their immunospecifity these polysaccharides share high structural similarity. Both are composed of the same monosaccharide residues and differ only in the connection of the Neu5Acα2‐3Gal side chain to the GlcNAc unit, which is a β1‐4 linkage in serotype Ia and a β1‐3 linkage in serotype Ib. The development of efficient regioselective routes for GlcNAcβ1‐3[Glcβ1‐4]Gal synthons is described, which give access to different group B Streptococcus (GBS) Ia and Ib repeating unit frameshifts. These glycans were used to probe the conformation and molecular dynamics of the two polysaccharides, highlighting the different presentation of the protruding Neu5Acα2‐3Gal moieties on the polysaccharide backbones and a higher flexibility of Ib polymer relative to Ia, which can impact epitope exposure.
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spelling pubmed-69729932020-01-27 Regioselective Glycosylation Strategies for the Synthesis of Group Ia and Ib Streptococcus Related Glycans Enable Elucidating Unique Conformations of the Capsular Polysaccharides Del Bino, Linda Calloni, Ilaria Oldrini, Davide Raso, Maria Michelina Cuffaro, Rossella Ardá, Ana Codée, Jeroen D. C. Jiménez‐Barbero, Jesús Adamo, Roberto Chemistry Full Papers Group B Streptococcus serotypes Ia and Ib capsular polysaccharides are key targets for vaccine development. In spite of their immunospecifity these polysaccharides share high structural similarity. Both are composed of the same monosaccharide residues and differ only in the connection of the Neu5Acα2‐3Gal side chain to the GlcNAc unit, which is a β1‐4 linkage in serotype Ia and a β1‐3 linkage in serotype Ib. The development of efficient regioselective routes for GlcNAcβ1‐3[Glcβ1‐4]Gal synthons is described, which give access to different group B Streptococcus (GBS) Ia and Ib repeating unit frameshifts. These glycans were used to probe the conformation and molecular dynamics of the two polysaccharides, highlighting the different presentation of the protruding Neu5Acα2‐3Gal moieties on the polysaccharide backbones and a higher flexibility of Ib polymer relative to Ia, which can impact epitope exposure. John Wiley and Sons Inc. 2019-11-04 2019-12-18 /pmc/articles/PMC6972993/ /pubmed/31506992 http://dx.doi.org/10.1002/chem.201903527 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. 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
Del Bino, Linda
Calloni, Ilaria
Oldrini, Davide
Raso, Maria Michelina
Cuffaro, Rossella
Ardá, Ana
Codée, Jeroen D. C.
Jiménez‐Barbero, Jesús
Adamo, Roberto
Regioselective Glycosylation Strategies for the Synthesis of Group Ia and Ib Streptococcus Related Glycans Enable Elucidating Unique Conformations of the Capsular Polysaccharides
title Regioselective Glycosylation Strategies for the Synthesis of Group Ia and Ib Streptococcus Related Glycans Enable Elucidating Unique Conformations of the Capsular Polysaccharides
title_full Regioselective Glycosylation Strategies for the Synthesis of Group Ia and Ib Streptococcus Related Glycans Enable Elucidating Unique Conformations of the Capsular Polysaccharides
title_fullStr Regioselective Glycosylation Strategies for the Synthesis of Group Ia and Ib Streptococcus Related Glycans Enable Elucidating Unique Conformations of the Capsular Polysaccharides
title_full_unstemmed Regioselective Glycosylation Strategies for the Synthesis of Group Ia and Ib Streptococcus Related Glycans Enable Elucidating Unique Conformations of the Capsular Polysaccharides
title_short Regioselective Glycosylation Strategies for the Synthesis of Group Ia and Ib Streptococcus Related Glycans Enable Elucidating Unique Conformations of the Capsular Polysaccharides
title_sort regioselective glycosylation strategies for the synthesis of group ia and ib streptococcus related glycans enable elucidating unique conformations of the capsular polysaccharides
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972993/
https://www.ncbi.nlm.nih.gov/pubmed/31506992
http://dx.doi.org/10.1002/chem.201903527
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