Assembly of Bionanostructures onto β-Cyclodextrin Molecular Printboards for Antibody Recognition and Lymphocyte Cell Counting

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Ludden, Manon J.W. and Li, Xiao and Greve, Jan and Amerongen, Aart van and Escalante, Maryana and Subramaniam, Vinod and Reinhoudt, David N. and Huskens, Jurriaan (2008) Assembly of Bionanostructures onto β-Cyclodextrin Molecular Printboards for Antibody Recognition and Lymphocyte Cell Counting. Journal of the American Chemical Society, 130 (22). pp. 6964-6973. ISSN 0002-7863

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Abstract:The assembly of complex bionanostructures onto β-cyclodextrin (βCD) monolayers has been investigated with the aims of antibody recognition and cell adhesion. The formation of these assemblies relies on host−guest, protein−ligand, and protein−protein interactions. The buildup of a structure consisting of a divalent bis(adamantyl)-biotin linker, streptavidin (SAv), biotinylated protein A (bt-PA), and an Fc fragment of a human immunoglobin G (IgG-Fc) was studied with surface plasmon resonance (SPR) spectroscopy. Patterns of this bionanostructure were obtained via microcontact printing of the divalent linker at the molecular printboard, followed by the subsequent attachment of the proteins. Fluorescence microscopy showed that the buildup of these bionanostructures on the βCD monolayers is highly specific. On the basis of these results, bionanostructures were made in which whole antibodies (ABs) were used instead of the IgG-Fc. These ABs were bound to the SAv layer via biotinylated protein G (bt-PG) or via a biotinylated AB. These constructions yielded specifically bound ABs with a less than maximal density, as shown by SPR spectroscopy and atomic force microscopy (AFM). Finally, the immobilization of ABs to the molecular printboard was used to create platforms for lymphocyte cell count purposes. Monoclonal ABs (MABs) were attached to the SAv layer using bt-PG, an engineered biotin functionality, or through nonspecific adsorption. The binding specificity of the immobilized cells was the highest on the buildup made from bt-PG, which is attributed to an optimized orientation of the antibodies. An approximately linear relationship between the numbers of seeded cells and counted cells was demonstrated, rendering the platform potentially suitable for lymphocyte cell counting.
Item Type:Article
Copyright:© 2008 American Chemical Society
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Science and Technology (TNW)
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Link to this item:http://purl.utwente.nl/publications/72207
Official URL:http://dx.doi.org/10.1021/ja078109v
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