Cargando…

Presenting Precision Glycomacromolecules on Gold Nanoparticles for Increased Lectin Binding

Glyco-functionalized gold nanoparticles have great potential as biosensors and as inhibitors due to their increased binding to carbohydrate-recognizing receptors such as the lectins. Here we apply previously developed solid phase polymer synthesis to obtain a series of precision glycomacromolecules...

Descripción completa

Detalles Bibliográficos
Autores principales: Boden, Sophia, Wagner, Kristina G., Karg, Matthias, Hartmann, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418785/
https://www.ncbi.nlm.nih.gov/pubmed/30966014
http://dx.doi.org/10.3390/polym9120716
_version_ 1783403805939859456
author Boden, Sophia
Wagner, Kristina G.
Karg, Matthias
Hartmann, Laura
author_facet Boden, Sophia
Wagner, Kristina G.
Karg, Matthias
Hartmann, Laura
author_sort Boden, Sophia
collection PubMed
description Glyco-functionalized gold nanoparticles have great potential as biosensors and as inhibitors due to their increased binding to carbohydrate-recognizing receptors such as the lectins. Here we apply previously developed solid phase polymer synthesis to obtain a series of precision glycomacromolecules that allows for straightforward variation of their chemical structure as well as functionalization of gold nanoparticles by ligand exchange. A novel building block is introduced allowing for the change of spacer building blocks within the macromolecular scaffold going from an ethylene glycol unit to an aliphatic spacer. Furthermore, the valency and overall length of the glycomacromolecule is varied. All glyco-functionalized gold nanoparticles show high degree of functionalization along with high stability in buffer solution. Therefore, a series of measurements applying UV-Vis spectroscopy, dynamic light scattering (DLS) and surface plasmon resonance (SPR) were performed studying the aggregation behavior of the glyco-functionalized gold nanoparticles in presence of model lectin Concanavalin A. While the multivalent presentation of glycomacromolecules on gold nanoparticles (AuNPs) showed a strong increase in binding compared to the free ligands, we also observed an influence of the chemical structure of the ligand such as its valency or hydrophobicity on the resulting lectin interactions. The straightforward variation of the chemical structure of the precision glycomacromolecule thus gives access to tailor-made glyco-gold nanoparticles (glyco-AuNPs) and fine-tuning of their lectin binding properties.
format Online
Article
Text
id pubmed-6418785
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-64187852019-04-02 Presenting Precision Glycomacromolecules on Gold Nanoparticles for Increased Lectin Binding Boden, Sophia Wagner, Kristina G. Karg, Matthias Hartmann, Laura Polymers (Basel) Article Glyco-functionalized gold nanoparticles have great potential as biosensors and as inhibitors due to their increased binding to carbohydrate-recognizing receptors such as the lectins. Here we apply previously developed solid phase polymer synthesis to obtain a series of precision glycomacromolecules that allows for straightforward variation of their chemical structure as well as functionalization of gold nanoparticles by ligand exchange. A novel building block is introduced allowing for the change of spacer building blocks within the macromolecular scaffold going from an ethylene glycol unit to an aliphatic spacer. Furthermore, the valency and overall length of the glycomacromolecule is varied. All glyco-functionalized gold nanoparticles show high degree of functionalization along with high stability in buffer solution. Therefore, a series of measurements applying UV-Vis spectroscopy, dynamic light scattering (DLS) and surface plasmon resonance (SPR) were performed studying the aggregation behavior of the glyco-functionalized gold nanoparticles in presence of model lectin Concanavalin A. While the multivalent presentation of glycomacromolecules on gold nanoparticles (AuNPs) showed a strong increase in binding compared to the free ligands, we also observed an influence of the chemical structure of the ligand such as its valency or hydrophobicity on the resulting lectin interactions. The straightforward variation of the chemical structure of the precision glycomacromolecule thus gives access to tailor-made glyco-gold nanoparticles (glyco-AuNPs) and fine-tuning of their lectin binding properties. MDPI 2017-12-14 /pmc/articles/PMC6418785/ /pubmed/30966014 http://dx.doi.org/10.3390/polym9120716 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Boden, Sophia
Wagner, Kristina G.
Karg, Matthias
Hartmann, Laura
Presenting Precision Glycomacromolecules on Gold Nanoparticles for Increased Lectin Binding
title Presenting Precision Glycomacromolecules on Gold Nanoparticles for Increased Lectin Binding
title_full Presenting Precision Glycomacromolecules on Gold Nanoparticles for Increased Lectin Binding
title_fullStr Presenting Precision Glycomacromolecules on Gold Nanoparticles for Increased Lectin Binding
title_full_unstemmed Presenting Precision Glycomacromolecules on Gold Nanoparticles for Increased Lectin Binding
title_short Presenting Precision Glycomacromolecules on Gold Nanoparticles for Increased Lectin Binding
title_sort presenting precision glycomacromolecules on gold nanoparticles for increased lectin binding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418785/
https://www.ncbi.nlm.nih.gov/pubmed/30966014
http://dx.doi.org/10.3390/polym9120716
work_keys_str_mv AT bodensophia presentingprecisionglycomacromoleculesongoldnanoparticlesforincreasedlectinbinding
AT wagnerkristinag presentingprecisionglycomacromoleculesongoldnanoparticlesforincreasedlectinbinding
AT kargmatthias presentingprecisionglycomacromoleculesongoldnanoparticlesforincreasedlectinbinding
AT hartmannlaura presentingprecisionglycomacromoleculesongoldnanoparticlesforincreasedlectinbinding