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Biosensors: Control of Nanoscale Environment to Improve Stability of Immobilized Proteins on Diamond Surfaces (Adv. Funct. Mater. 6/2011)
Article first published online: 18 MAR 2011
DOI: 10.1002/adfm.201190011
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Radadia, A. D., Stavis, C. J., Carr, R., Zeng, H., King, W. P., Carlisle, J. A., Aksimentiev, A., Hamers, R. J. and Bashir, R. (2011), Biosensors: Control of Nanoscale Environment to Improve Stability of Immobilized Proteins on Diamond Surfaces (Adv. Funct. Mater. 6/2011). Advanced Functional Materials, 21: 1008. doi: 10.1002/adfm.201190011
Publication History
- Issue published online: 18 MAR 2011
- Article first published online: 18 MAR 2011
- Abstract
- Cited By
Keywords:
- diamond thin films;
- biofunctionalized diamond;
- diamond biosensors;
- ultrananocrystalline diamond;
- proteins
Graphical Abstract

Immunoassays for the detection of bacterial pathogens rely on the selectivity and stability of biorecognition elements, such as antibodies tethered to sensor surfaces. on page 1040, Robert J. Hamers, Rashid Bashir, and co-workers show that covalent linking of antibodies to diamond surfaces leads to substantial improvements in the biological activity of proteins. The results can be easily extended to the functionalization of micro- and nanodi-mensional sensors and structures of biomedical diagnostic and therapeutic interest.
Abstract
Immunoassays for detection of bacterial pathogens rely on the selectivity and stability of bio-recognition elements such as antibodies tethered to sensor surfaces. The search for novel surfaces that improve the stability of biomolecules and assay performance has been pursued for a long time. However, the anticipated improvements in stability have not been realized in practice under physiological conditions because the surface functionalization layers on commonly used substrates, silica and gold, are themselves unstable on time scales of days. In this paper, we show that covalent linking of antibodies to diamond surfaces leads to substantial improvements in biological activity of proteins as measured by the ability to selectively capture cells of the pathogenic bacterium Escherichia coli O157:H7 even after exposure to buffer solutions at 37 ºC for extended periods of time, approaching 2 weeks. Our results from ELISA, XPS, fluorescence microscopy, and MD simulations suggest that by using highly stable surface chemistry and controlling the nanoscale organization of the antibodies on the surface, it is possible to achieve significant improvements in biological activity and stability. Our findings can be easily extended to functionalization of micro and nanodimensional sensors and structures of biomedical diagnostic and therapeutic interest.

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