Research Article
Nanoscale positioning of inorganic nanoparticles using biological ferritin arrays fabricated by dip-pen nanolithography
Article first published online: 12 JAN 2010
DOI: 10.1002/sca.20162
Copyright © 2010 Wiley Periodicals, Inc.
Issue

Scanning
Special Issue: Advancing Dip Pen Nanolithography
Volume 32, Issue 1, pages 35–41, January/February 2010
Additional Information
How to Cite
Bellido, E., de Miguel, R., Sesé, J., Ruiz-Molina, D., Lostao, A. and Maspoch, D. (2010), Nanoscale positioning of inorganic nanoparticles using biological ferritin arrays fabricated by dip-pen nanolithography. Scanning, 32: 35–41. doi: 10.1002/sca.20162
Publication History
- Issue published online: 18 MAY 2010
- Article first published online: 12 JAN 2010
- Manuscript Accepted: 26 NOV 2009
- Manuscript Received: 10 NOV 2009
Funded by
- MAT2009-13977-C03
- Nanomateria-DGA, PI091/08
- Ministerio de Ciencia y Tecnología
- ARAID
- Abstract
- References
- Cited By
Keywords:
- dip-pen nanolithography;
- nanoarrays;
- iron oxide nanoparticles;
- ferritin;
- bio-template
Abstract
In this manuscript we demonstrate the spatially controlled immobilization of ferritin proteins by directly writing them on a wide range of substrates of technological interest. Optical and fluorescence microscopy, AFM and TOF-SIMS studies confirm the successful deposition of the protein on those surfaces. Control on nanostructure shape and size, by miniaturizing the dot-like features down to a 100 nm, demonstrates the particular capabilities of the DPN approach. Ultimately, this study gives the opportunity to design nanoparticle-based arrays regarding the growing interest in the use of nanoparticles as structural and functional elements for fabricating nanodevices. Herein, we demonstrate how the protein shell of ferritins can be removed by a simple heat-treatment process while maintaining the encapsulated inorganic nanoparticle intact on the same location of the nanoarray. As a result, this study establishes how direct-write DPN approach could give the opportunity to design not only protein-based nanoarrays but also nanoparticle-based nanoarrays with high-resolution and control. SCANNING 32: 35–41, 2010. © 2010 Wiley Periodicals, Inc.

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