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Oligonucleotide Metallization for Conductive Bio-Inorganic Interfaces in Self Assembled Nanoelectronics and Nanosystems

Published online by Cambridge University Press:  01 February 2011

Xu Wang
Affiliation:
Chemical and Environmental Engineering Department
Krishna Singh
Affiliation:
Chemical and Environmental Engineering Department
Chris Tsai
Affiliation:
Electrical Engineering Department; Cengiz Ozkan, Mechanical Engineering Department; University of California, Riverside, 92521USA
Roger Lake
Affiliation:
Electrical Engineering Department; Cengiz Ozkan, Mechanical Engineering Department; University of California, Riverside, 92521USA
Alexander Balandin
Affiliation:
Electrical Engineering Department; Cengiz Ozkan, Mechanical Engineering Department; University of California, Riverside, 92521USA
Mihri Ozkan
Affiliation:
Electrical Engineering Department; Cengiz Ozkan, Mechanical Engineering Department; University of California, Riverside, 92521USA
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Abstract

Properly designed sequences of oligonucleotides can be employed as scaffolds or templates for the self-organization of nanostructures and devices, through the Watson-Crick base pairing mechanism which serves as a programmable smart glue. In this paper, we report the Platinum metallization of peptide nucleic acid (PNA) sequences for the first time. PNA is an analogue of DNA and has a neutral backbone which provides stronger hybridization, greater stability and higher specificity in base pairing. Pt ions were reduced from a salt solution and localized over the PNA fragments where the size of the Pt colloids depends on the duration of chemical reduction. Computations of the high lying occupied and lowlying unoccupied orbitals indicated that Pt nanoparticles bind easily on both the Thymine (T) bases and the backbone in the PNA.

Type
Research Article
Copyright
Copyright © Materials Research Society 2005

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References

[1] Niemeyer, C. M., et al. Angew. Chem. Int. Ed, 40, 41284158 (2001).Google Scholar
[2] Egholm, M., Buchardt, O. et al. Nature, 365, 566568 (1993).Google Scholar
[3] Egholm, M., Nielsen, P. E., Buchardt, O., and Berg, R. H., J. Am.Chem. Soc., 114, 96779678(1992).Google Scholar
[4] Arkin, M. R., Science 273, 475(1996).Google Scholar
[5] Okahata, Y., Kobayashi, T., Tanaka, K., and Shimomura, M., J. Am. Chem.Soc., 120, (6165~1998).Google Scholar
[6] Jortner, J., Bixon, M., Langenbacher, T., and Michel-Beyerle, M. E., Proc.Natl. Acad. Sci. U.S.A. 95, 12759 (1998).Google Scholar
[7] Meggers, E., Michel-Beyerle, M. E., and Giese, B., J. Am. Chem. Soc. 120, 12950 (1998).Google Scholar
[8] Pablo, P. J. de. et al, Phys. Rev. Lett., 85, 4992 (2000).Google Scholar
[9] Henderson, P. T., Jones, D., Hampikian, G., Kann, Y., and Shuster, B. G., Proc. Natl. Acad. Sci. U.S.A. 96, 8353 (1999).Google Scholar
[10]Porath, D., Bezryadin, A., Vries, S. de, and Dekker, C., Nature, 403, 635 (2000).Google Scholar
[11] Braun, Erez, Eichen, Yoav, Sivan, Uri, Ben-Yoseph, Gdalyahu, Nature, 391, 775778 (1998).Google Scholar
[12] Richter, Jan, Mertig, Michael, and Pompe, Wolfgang. Applied Physics Letters, 78, 536538 (2001).Google Scholar
[13] Becke, A. D., J. Chem. Phys., 98, 5648 (1993).Google Scholar
[14] Hay, P.J. and Wadt, W.R., J.Chem. Phys., 82, 270(1985).Google Scholar
[15] Wadt, W. R., and Hay, P. J., J. Chem. Phys., 82, 284 (1985).Google Scholar
[16] Hay, P.J. and Wadt, W.R., J.Chem. Phys., 82, 299(1985).Google Scholar
[17] Frisch, M.J. et al., Gaussian 03, Revision B.03 (Gaussian Inc., Pittsburgh, 2003).Google Scholar
[18] Keren, K., Berman, R. S., and Braun, E., Nano Lett., 4, 323 (2004).Google Scholar