Molecular recognition of surface-immobilized carbohydrates by a synthetic lectin

The molecular recognition of carbohydrates and proteins mediates a wide range of physiological processes and the development of synthetic carbohydrate receptors (“synthetic lectins”) constitutes a key advance in biomedical technology. In this article we report a synthetic lectin that selectively bin...

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Main Authors: Melanie Rauschenberg, Eva-Corrina Fritz, Christian Schulz, Tobias Kaufmann, Bart Jan Ravoo
Format: Article
Language:English
Published: Beilstein-Institut 2014-06-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.10.138
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author Melanie Rauschenberg
Eva-Corrina Fritz
Christian Schulz
Tobias Kaufmann
Bart Jan Ravoo
author_facet Melanie Rauschenberg
Eva-Corrina Fritz
Christian Schulz
Tobias Kaufmann
Bart Jan Ravoo
author_sort Melanie Rauschenberg
collection DOAJ
description The molecular recognition of carbohydrates and proteins mediates a wide range of physiological processes and the development of synthetic carbohydrate receptors (“synthetic lectins”) constitutes a key advance in biomedical technology. In this article we report a synthetic lectin that selectively binds to carbohydrates immobilized in a molecular monolayer. Inspired by our previous work, we prepared a fluorescently labeled synthetic lectin consisting of a cyclic dimer of the tripeptide Cys-His-Cys, which forms spontaneously by air oxidation of the monomer. Amine-tethered derivatives of N-acetylneuraminic acid (NANA), β-D-galactose, β-D-glucose and α-D-mannose were microcontact printed on epoxide-terminated self-assembled monolayers. Successive prints resulted in simple microarrays of two carbohydrates. The selectivity of the synthetic lectin was investigated by incubation on the immobilized carbohydrates. Selective binding of the synthetic lectin to immobilized NANA and β-D-galactose was observed by fluorescence microscopy. The selectivity and affinity of the synthetic lectin was screened in competition experiments. In addition, the carbohydrate binding of the synthetic lectin was compared with the carbohydrate binding of the lectins concanavalin A and peanut agglutinin. It was found that the printed carbohydrates retain their characteristic selectivity towards the synthetic and natural lectins and that the recognition of synthetic and natural lectins is strictly orthogonal.
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spelling doaj.art-f6540b3918854b539ad6340aff2ab4682022-12-21T17:14:33ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972014-06-011011354136410.3762/bjoc.10.1381860-5397-10-138Molecular recognition of surface-immobilized carbohydrates by a synthetic lectinMelanie Rauschenberg0Eva-Corrina Fritz1Christian Schulz2Tobias Kaufmann3Bart Jan Ravoo4Organic Chemistry Institute, Westfälische Wilhelms-Universität Münster, Corrensstrasse 40, 48149 Münster, GermanyOrganic Chemistry Institute, Westfälische Wilhelms-Universität Münster, Corrensstrasse 40, 48149 Münster, GermanyOrganic Chemistry Institute, Westfälische Wilhelms-Universität Münster, Corrensstrasse 40, 48149 Münster, GermanyOrganic Chemistry Institute, Westfälische Wilhelms-Universität Münster, Corrensstrasse 40, 48149 Münster, GermanyOrganic Chemistry Institute, Westfälische Wilhelms-Universität Münster, Corrensstrasse 40, 48149 Münster, GermanyThe molecular recognition of carbohydrates and proteins mediates a wide range of physiological processes and the development of synthetic carbohydrate receptors (“synthetic lectins”) constitutes a key advance in biomedical technology. In this article we report a synthetic lectin that selectively binds to carbohydrates immobilized in a molecular monolayer. Inspired by our previous work, we prepared a fluorescently labeled synthetic lectin consisting of a cyclic dimer of the tripeptide Cys-His-Cys, which forms spontaneously by air oxidation of the monomer. Amine-tethered derivatives of N-acetylneuraminic acid (NANA), β-D-galactose, β-D-glucose and α-D-mannose were microcontact printed on epoxide-terminated self-assembled monolayers. Successive prints resulted in simple microarrays of two carbohydrates. The selectivity of the synthetic lectin was investigated by incubation on the immobilized carbohydrates. Selective binding of the synthetic lectin to immobilized NANA and β-D-galactose was observed by fluorescence microscopy. The selectivity and affinity of the synthetic lectin was screened in competition experiments. In addition, the carbohydrate binding of the synthetic lectin was compared with the carbohydrate binding of the lectins concanavalin A and peanut agglutinin. It was found that the printed carbohydrates retain their characteristic selectivity towards the synthetic and natural lectins and that the recognition of synthetic and natural lectins is strictly orthogonal.https://doi.org/10.3762/bjoc.10.138carbohydrateslectinsmolecular recognitionmicroarraysmultivalent glycosystemspeptides
spellingShingle Melanie Rauschenberg
Eva-Corrina Fritz
Christian Schulz
Tobias Kaufmann
Bart Jan Ravoo
Molecular recognition of surface-immobilized carbohydrates by a synthetic lectin
Beilstein Journal of Organic Chemistry
carbohydrates
lectins
molecular recognition
microarrays
multivalent glycosystems
peptides
title Molecular recognition of surface-immobilized carbohydrates by a synthetic lectin
title_full Molecular recognition of surface-immobilized carbohydrates by a synthetic lectin
title_fullStr Molecular recognition of surface-immobilized carbohydrates by a synthetic lectin
title_full_unstemmed Molecular recognition of surface-immobilized carbohydrates by a synthetic lectin
title_short Molecular recognition of surface-immobilized carbohydrates by a synthetic lectin
title_sort molecular recognition of surface immobilized carbohydrates by a synthetic lectin
topic carbohydrates
lectins
molecular recognition
microarrays
multivalent glycosystems
peptides
url https://doi.org/10.3762/bjoc.10.138
work_keys_str_mv AT melanierauschenberg molecularrecognitionofsurfaceimmobilizedcarbohydratesbyasyntheticlectin
AT evacorrinafritz molecularrecognitionofsurfaceimmobilizedcarbohydratesbyasyntheticlectin
AT christianschulz molecularrecognitionofsurfaceimmobilizedcarbohydratesbyasyntheticlectin
AT tobiaskaufmann molecularrecognitionofsurfaceimmobilizedcarbohydratesbyasyntheticlectin
AT bartjanravoo molecularrecognitionofsurfaceimmobilizedcarbohydratesbyasyntheticlectin