Gold Glyconanoparticles: Synthetic Polyvalent Ligands Mimicking Glycocalyx‐Like Surfaces as Tools for Glycobiological Studies
- 9 April 2003
- journal article
- research article
- Published by Wiley in Chemistry – A European Journal
- Vol. 9 (9) , 1909-1921
- https://doi.org/10.1002/chem.200204544
Abstract
A simple and versatile methodology is described for tailoring sugar-functionalised gold nanoclusters (glyconanoparticles) that have 3D polyvalent carbohydrate display and globular shapes. This methodology allows the preparation of glyconanoparticles with biologically significant oligosaccharides as well as with differing carbohydrate density. Fluorescent glyconanoparticles have been also prepared for labelling cells in biological tests. The materials are water soluble, stable under physiological conditions and present an exceptional small core size. All of them have been characterised by 1H NMR, UV and IR spectroscopy, TEM and elemental analysis. Their highly polyvalent network can mimic glycosphingolipid clustering and interactions at the plasma membrane, providing an controlled system for glycobiological studies. Furthermore, they are useful building blocks for the design of nanomaterials.Keywords
This publication has 41 references indexed in Scilit:
- A Quantitative Estimation of Carbohydrate-Carbohydrate Interaction Using Clustered Oligosaccharides of Glycolipid Monolayers and of Artificial Glycoconjugate Polymers by Surface Plasmon ResonanceJournal of the American Chemical Society, 2000
- A surface chemistry approach to studying cell adhesionChemical Society Reviews, 2000
- Water-Soluble, Isolable Gold Clusters Protected by Tiopronin and Coenzyme A MonolayersLangmuir, 1998
- Carbohydrate−Carbohydrate Interactions in Water with Glycophanes as Model SystemsThe Journal of Organic Chemistry, 1998
- Polyvalent Interactions in Biological Systems: Implications for Design and Use of Multivalent Ligands and InhibitorsAngewandte Chemie International Edition in English, 1998
- Molecular Recognition of Carbohydrates Using a Synthetic Receptor. A Model System to Understand the Stereoselectivity of a Carbohydrate-Carbohydrate Interaction in WaterJournal of the American Chemical Society, 1995
- Synthesis of thiol-derivatised gold nanoparticles in a two-phase Liquid–Liquid systemJournal of the Chemical Society, Chemical Communications, 1994
- The solution conformation of the Leχ groupBiochemical and Biophysical Research Communications, 1991
- Glycoconjugate expression during embryogenesis and its biological significanceBioEssays, 1990
- Abbau der reduzierenden Biosen, VII.: Konstitutions‐Ermittlung der MaltoseBerichte der deutschen chemischen Gesellschaft (A and B Series), 1927