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Photoswitchable precision glycooligomers and their lectin binding

The synthesis of photoswitchable glycooligomers is presented by applying solid-phase polymer synthesis and functional building blocks. The obtained glycoligands are monodisperse and present azobenzene moieties as well as sugar ligands at defined positions within the oligomeric backbone and side chai...

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Autores principales: Ponader, Daniela, Igde, Sinaida, Wehle, Marko, Märker, Katharina, Santer, Mark, Bléger, David, Hartmann, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143111/
https://www.ncbi.nlm.nih.gov/pubmed/25161717
http://dx.doi.org/10.3762/bjoc.10.166
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author Ponader, Daniela
Igde, Sinaida
Wehle, Marko
Märker, Katharina
Santer, Mark
Bléger, David
Hartmann, Laura
author_facet Ponader, Daniela
Igde, Sinaida
Wehle, Marko
Märker, Katharina
Santer, Mark
Bléger, David
Hartmann, Laura
author_sort Ponader, Daniela
collection PubMed
description The synthesis of photoswitchable glycooligomers is presented by applying solid-phase polymer synthesis and functional building blocks. The obtained glycoligands are monodisperse and present azobenzene moieties as well as sugar ligands at defined positions within the oligomeric backbone and side chains, respectively. We show that the combination of molecular precision together with the photoswitchable properties of the azobenzene unit allows for the photosensitive control of glycoligand binding to protein receptors. These stimuli-sensitive glycoligands promote the understanding of multivalent binding and will be further developed as novel biosensors.
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spelling pubmed-41431112014-08-26 Photoswitchable precision glycooligomers and their lectin binding Ponader, Daniela Igde, Sinaida Wehle, Marko Märker, Katharina Santer, Mark Bléger, David Hartmann, Laura Beilstein J Org Chem Full Research Paper The synthesis of photoswitchable glycooligomers is presented by applying solid-phase polymer synthesis and functional building blocks. The obtained glycoligands are monodisperse and present azobenzene moieties as well as sugar ligands at defined positions within the oligomeric backbone and side chains, respectively. We show that the combination of molecular precision together with the photoswitchable properties of the azobenzene unit allows for the photosensitive control of glycoligand binding to protein receptors. These stimuli-sensitive glycoligands promote the understanding of multivalent binding and will be further developed as novel biosensors. Beilstein-Institut 2014-07-15 /pmc/articles/PMC4143111/ /pubmed/25161717 http://dx.doi.org/10.3762/bjoc.10.166 Text en Copyright © 2014, Ponader et al. 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 Full Research Paper
Ponader, Daniela
Igde, Sinaida
Wehle, Marko
Märker, Katharina
Santer, Mark
Bléger, David
Hartmann, Laura
Photoswitchable precision glycooligomers and their lectin binding
title Photoswitchable precision glycooligomers and their lectin binding
title_full Photoswitchable precision glycooligomers and their lectin binding
title_fullStr Photoswitchable precision glycooligomers and their lectin binding
title_full_unstemmed Photoswitchable precision glycooligomers and their lectin binding
title_short Photoswitchable precision glycooligomers and their lectin binding
title_sort photoswitchable precision glycooligomers and their lectin binding
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4143111/
https://www.ncbi.nlm.nih.gov/pubmed/25161717
http://dx.doi.org/10.3762/bjoc.10.166
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