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dc.contributor.authorPiana, Stefano
dc.date.accessioned2017-01-30T13:04:04Z
dc.date.available2017-01-30T13:04:04Z
dc.date.created2008-11-12T23:24:53Z
dc.date.issued2005
dc.identifier.citationPiana, Stefano. 2005. Structure and energy of a DNA dodecamer under tensile load. Nucleic Acids Research 33: 7029-7038.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/28262
dc.identifier.doi10.1093/nar/gki1010
dc.description.abstract

In the last decade, methods to study single DNA molecules under tensile load have been developed. These experiments measure the force required to stretch and melt the double helix and provide insights into the structural stability of DNA. However, it is not easy to directly relate the shape of the force curve to the structural changes that occur in the double helix under tensile load. Here, state-of-the-art computer simulations of short DNA sequences are preformed to provide an atomistic description of the stretching of the DNA double helix. These calculations show that for extensions larger that ~25% the DNA undergoes a structural transformation and a few base pairs are lost from both the terminal and central part of the helix. This locally melted DNA duplex is stable and can be extended up to ~50-60% of the equilibrium length at a constant force. It is concluded that melting under tension cannot be modeled as a simple two-state process. Finally, the important role of the cantilever stiffness in determining the shape of the force- extension curve and the most probable rupture force is discussed.

dc.publisherOxford University Press
dc.titleStructure and energy of a DNA dodecamer under tensile load
dc.typeJournal Article
dcterms.source.volume33
dcterms.source.startPage7029
dcterms.source.endPage7038
dcterms.source.titleNucleic Acids Research
curtin.note

This is a pre-copy-editing, author-produced PDF of an article accepted for publication in Nucleic Acids Research following peer review. The definitive publisher-authenticated version is available online at: http://dx.doi.org/doi:10.1093/nar/gki1010

curtin.identifierEPR-660
curtin.accessStatusOpen access
curtin.facultyDepartment of Applied Chemistry
curtin.facultyDivision of Engineering, Science and Computing
curtin.facultyFaculty of Science


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