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dc.contributor.authorPiana, Stefano
dc.contributor.authorBilic, Ante
dc.date.accessioned2017-01-30T13:41:21Z
dc.date.available2017-01-30T13:41:21Z
dc.date.created2008-11-12T23:32:23Z
dc.date.issued2006
dc.identifier.citationPiana-agostinetti, Stefano and Bilic, Ante. 2006. The Nature of the Adsorption of Nucleobases on the Gold [111] Surface. Journal of Physical Chemistry B 110: 23467-23471.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/34124
dc.description.abstract

Biochip technology is based on the immobilization of biological macromolecules on the surface of electronic devices. The biochemical properties of the immobilized molecules can be influenced to a large extent by the interaction with the inorganic surface. The interaction of DNA with the surface of gold, a metal commonly used in biochip technologies, is sequence dependent as the four nucleobases, adenine, thymine, cytosine, and guanine, interact to a different extent with the gold surface. The nature of nucleobase adsorption on the gold [111] surface has been investigated by performing density functional theory and post-Hartree-Fock calculations. It turns out that the interaction is dominated by dispersion forces and an appreciable degree of chemisorption is observed for adenine only. A set of Lennard-Jones parameters that describe the interaction was derived from the post-Hartree-Fock calculations. Classical molecular dynamics simulations of nucleobase monolayers based on these parameters are in remarkable agreement with the experiment and show that the interaction of the nucleobases with the gold surface is strongly modulated by base-base interations and reaches a maximum when a full monolayer is formed.

dc.publisherAmerican Chemical Society
dc.relation.urihttp://pubs.acs.org/journals/jpcbfk/index.html
dc.relation.urihttp://pubs.acs.org/cgi-bin/article.cgi/jpcbfk/2006/110/i46/pdf/jp064438i.pdf
dc.titleThe Nature of the Adsorption of Nucleobases on the Gold [111] Surface
dc.typeJournal Article
dcterms.source.volume110
dcterms.source.startPage23467
dcterms.source.endPage23471
dcterms.source.titleJournal of Physical Chemistry B
curtin.note

Open access to this article available via the website of the American Chemical Society. http://acswebcontent.acs.org/home.html

curtin.note

The website for the Journal of Physical Chemistry B Society is available at:

curtin.note

http://pubs.acs.org/journals/jpcbfk/index.html

curtin.identifierEPR-1282
curtin.accessStatusFulltext not available
curtin.facultyDepartment of Applied Chemistry
curtin.facultyDivision of Engineering, Science and Computing
curtin.facultyFaculty of Science


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