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DNA display of glycoconjugates to emulate oligomeric interactions of glycans

Glycans (carbohydrate portion of glycoproteins and glycolipids) frequently exert their function through oligomeric interactions involving multiple carbohydrate units. In efforts to recapitulate the diverse spatial arrangements of the carbohydrate units, assemblies based on hybridization of nucleic a...

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Detalles Bibliográficos
Autores principales: Novoa, Alexandre, Winssinger, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462854/
https://www.ncbi.nlm.nih.gov/pubmed/26113879
http://dx.doi.org/10.3762/bjoc.11.81
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author Novoa, Alexandre
Winssinger, Nicolas
author_facet Novoa, Alexandre
Winssinger, Nicolas
author_sort Novoa, Alexandre
collection PubMed
description Glycans (carbohydrate portion of glycoproteins and glycolipids) frequently exert their function through oligomeric interactions involving multiple carbohydrate units. In efforts to recapitulate the diverse spatial arrangements of the carbohydrate units, assemblies based on hybridization of nucleic acid conjugates have been used to display simplified ligands with tailored interligand distances and valences. The programmability of the assemblies lends itself to a combinatorial display of multiple ligands. Recent efforts in the synthesis and applications of such conjugates are discussed.
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spelling pubmed-44628542015-06-25 DNA display of glycoconjugates to emulate oligomeric interactions of glycans Novoa, Alexandre Winssinger, Nicolas Beilstein J Org Chem Review Glycans (carbohydrate portion of glycoproteins and glycolipids) frequently exert their function through oligomeric interactions involving multiple carbohydrate units. In efforts to recapitulate the diverse spatial arrangements of the carbohydrate units, assemblies based on hybridization of nucleic acid conjugates have been used to display simplified ligands with tailored interligand distances and valences. The programmability of the assemblies lends itself to a combinatorial display of multiple ligands. Recent efforts in the synthesis and applications of such conjugates are discussed. Beilstein-Institut 2015-05-11 /pmc/articles/PMC4462854/ /pubmed/26113879 http://dx.doi.org/10.3762/bjoc.11.81 Text en Copyright © 2015, Novoa and Winssinger https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Review
Novoa, Alexandre
Winssinger, Nicolas
DNA display of glycoconjugates to emulate oligomeric interactions of glycans
title DNA display of glycoconjugates to emulate oligomeric interactions of glycans
title_full DNA display of glycoconjugates to emulate oligomeric interactions of glycans
title_fullStr DNA display of glycoconjugates to emulate oligomeric interactions of glycans
title_full_unstemmed DNA display of glycoconjugates to emulate oligomeric interactions of glycans
title_short DNA display of glycoconjugates to emulate oligomeric interactions of glycans
title_sort dna display of glycoconjugates to emulate oligomeric interactions of glycans
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4462854/
https://www.ncbi.nlm.nih.gov/pubmed/26113879
http://dx.doi.org/10.3762/bjoc.11.81
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