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Affinity Enhancement by Dendritic Side Chains in Synthetic Carbohydrate Receptors**

Dendritic side chains have been used to modify the binding environment in anthracene-based synthetic carbohydrate receptors. Control of length, charge, and branching enabled the positioning of side-chain carboxylate groups in such a way that they assisted in binding substrates rather than blocking t...

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Detalles Bibliográficos
Autores principales: Destecroix, Harry, Renney, Charles M, Mooibroek, Tiddo J, Carter, Tom S, Stewart, Patrick F N, Crump, Matthew P, Davis, Anthony P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506558/
https://www.ncbi.nlm.nih.gov/pubmed/25645064
http://dx.doi.org/10.1002/anie.201409124
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author Destecroix, Harry
Renney, Charles M
Mooibroek, Tiddo J
Carter, Tom S
Stewart, Patrick F N
Crump, Matthew P
Davis, Anthony P
author_facet Destecroix, Harry
Renney, Charles M
Mooibroek, Tiddo J
Carter, Tom S
Stewart, Patrick F N
Crump, Matthew P
Davis, Anthony P
author_sort Destecroix, Harry
collection PubMed
description Dendritic side chains have been used to modify the binding environment in anthracene-based synthetic carbohydrate receptors. Control of length, charge, and branching enabled the positioning of side-chain carboxylate groups in such a way that they assisted in binding substrates rather than blocking the cavity. Conformational degeneracy in the dendrimers resulted in effective preorganization despite the flexibility of the system. Strong binding was observed to glucosammonium ions in water, with K(a) values up to 7000 m(−1). Affinities for uncharged substrates (glucose and N-acetylglucosamine) were also enhanced, despite competition from solvent and the absence of electrostatic interactions.
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spelling pubmed-45065582015-07-22 Affinity Enhancement by Dendritic Side Chains in Synthetic Carbohydrate Receptors** Destecroix, Harry Renney, Charles M Mooibroek, Tiddo J Carter, Tom S Stewart, Patrick F N Crump, Matthew P Davis, Anthony P Angew Chem Int Ed Engl Communications Dendritic side chains have been used to modify the binding environment in anthracene-based synthetic carbohydrate receptors. Control of length, charge, and branching enabled the positioning of side-chain carboxylate groups in such a way that they assisted in binding substrates rather than blocking the cavity. Conformational degeneracy in the dendrimers resulted in effective preorganization despite the flexibility of the system. Strong binding was observed to glucosammonium ions in water, with K(a) values up to 7000 m(−1). Affinities for uncharged substrates (glucose and N-acetylglucosamine) were also enhanced, despite competition from solvent and the absence of electrostatic interactions. WILEY-VCH Verlag 2015-02-09 2015-01-21 /pmc/articles/PMC4506558/ /pubmed/25645064 http://dx.doi.org/10.1002/anie.201409124 Text en © 2015 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Destecroix, Harry
Renney, Charles M
Mooibroek, Tiddo J
Carter, Tom S
Stewart, Patrick F N
Crump, Matthew P
Davis, Anthony P
Affinity Enhancement by Dendritic Side Chains in Synthetic Carbohydrate Receptors**
title Affinity Enhancement by Dendritic Side Chains in Synthetic Carbohydrate Receptors**
title_full Affinity Enhancement by Dendritic Side Chains in Synthetic Carbohydrate Receptors**
title_fullStr Affinity Enhancement by Dendritic Side Chains in Synthetic Carbohydrate Receptors**
title_full_unstemmed Affinity Enhancement by Dendritic Side Chains in Synthetic Carbohydrate Receptors**
title_short Affinity Enhancement by Dendritic Side Chains in Synthetic Carbohydrate Receptors**
title_sort affinity enhancement by dendritic side chains in synthetic carbohydrate receptors**
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4506558/
https://www.ncbi.nlm.nih.gov/pubmed/25645064
http://dx.doi.org/10.1002/anie.201409124
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