Please use this identifier to cite or link to this item: https://doi.org/10.1166/jctn.2008.024
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dc.titleSequence-dependent unpeeling dynamics of stretched DNA double helix
dc.contributor.authorChen, H.
dc.contributor.authorFu, H.
dc.contributor.authorKoh, C.G.
dc.date.accessioned2014-06-17T08:24:42Z
dc.date.available2014-06-17T08:24:42Z
dc.date.issued2008-07
dc.identifier.citationChen, H., Fu, H., Koh, C.G. (2008-07). Sequence-dependent unpeeling dynamics of stretched DNA double helix. Journal of Computational and Theoretical Nanoscience 5 (7) : 1381-1386. ScholarBank@NUS Repository. https://doi.org/10.1166/jctn.2008.024
dc.identifier.issn15461955
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/66137
dc.description.abstractTo verify the theory of overstretching transition of DNA double helix developed by Cocco and coworkers, the overstretching processes of homopolymer, poly(GC) and poly(AT), and heteropolymer, λ DNA, are studied by a three-state Ising-like model. The three possible states are B-DNA, S-DNA, and unpeeled single ssDNA. Equilibrium property is obtained by transfer matrix method, while kinetic unpeeling process is studied by Monte Carlo simulation. For poly(GC) DNA, the unpeeling process begins from S-DNA at forces 200 pN if the extension rate is infinitely slow. At a finite extension rate, unpeeling forces can be much higher than 200 pN, which is dependent on the extension rate. For poly(AT) DNA, the unpeeling process begins from B-DNA, and the process is approximately in equilibrium at experimental accessible extension rate. For segment of λ DNA, unpeeling can begin at the B-S transition force, and it finishes at different forces depending on the extension rate. The results agree well with experiment. Copyright © 2008 American Scientific Publishers. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1166/jctn.2008.024
dc.sourceScopus
dc.subjectB-DNA
dc.subjectDNA overstretching
dc.subjectS-DNA
dc.subjectssDNA
dc.subjectUnpeeling
dc.typeArticle
dc.contributor.departmentPHYSICS
dc.contributor.departmentCIVIL ENGINEERING
dc.description.doi10.1166/jctn.2008.024
dc.description.sourcetitleJournal of Computational and Theoretical Nanoscience
dc.description.volume5
dc.description.issue7
dc.description.page1381-1386
dc.identifier.isiut000261210400024
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