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How Well Can DNA Rupture DNA? Shearing and Unzipping Forces inside DNA Nanostructures

[Image: see text] A purely DNA nanomachine must support internal stresses across short DNA segments with finite rigidity, producing effects that can be qualitatively very different from experimental observations of isolated DNA in fixed-force ensembles. In this article, computational simulations are...

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Detalles Bibliográficos
Autores principales: Tee, Shern Ren, Wang, Zhisong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044922/
https://www.ncbi.nlm.nih.gov/pubmed/30023776
http://dx.doi.org/10.1021/acsomega.7b01692
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author Tee, Shern Ren
Wang, Zhisong
author_facet Tee, Shern Ren
Wang, Zhisong
author_sort Tee, Shern Ren
collection PubMed
description [Image: see text] A purely DNA nanomachine must support internal stresses across short DNA segments with finite rigidity, producing effects that can be qualitatively very different from experimental observations of isolated DNA in fixed-force ensembles. In this article, computational simulations are used to study how well the rigidity of a driving DNA duplex can rupture a double-stranded DNA target into single-stranded segments and how well this stress can discriminate between unzipping or shearing geometries. This discrimination is found to be maximized at an optimal length but deteriorates as the driving duplex is either lengthened or shortened. This differs markedly from a fixed-force ensemble and has implications for the design parameters and limitations of dynamic DNA nanomachines.
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spelling pubmed-60449222018-07-16 How Well Can DNA Rupture DNA? Shearing and Unzipping Forces inside DNA Nanostructures Tee, Shern Ren Wang, Zhisong ACS Omega [Image: see text] A purely DNA nanomachine must support internal stresses across short DNA segments with finite rigidity, producing effects that can be qualitatively very different from experimental observations of isolated DNA in fixed-force ensembles. In this article, computational simulations are used to study how well the rigidity of a driving DNA duplex can rupture a double-stranded DNA target into single-stranded segments and how well this stress can discriminate between unzipping or shearing geometries. This discrimination is found to be maximized at an optimal length but deteriorates as the driving duplex is either lengthened or shortened. This differs markedly from a fixed-force ensemble and has implications for the design parameters and limitations of dynamic DNA nanomachines. American Chemical Society 2018-01-10 /pmc/articles/PMC6044922/ /pubmed/30023776 http://dx.doi.org/10.1021/acsomega.7b01692 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Tee, Shern Ren
Wang, Zhisong
How Well Can DNA Rupture DNA? Shearing and Unzipping Forces inside DNA Nanostructures
title How Well Can DNA Rupture DNA? Shearing and Unzipping Forces inside DNA Nanostructures
title_full How Well Can DNA Rupture DNA? Shearing and Unzipping Forces inside DNA Nanostructures
title_fullStr How Well Can DNA Rupture DNA? Shearing and Unzipping Forces inside DNA Nanostructures
title_full_unstemmed How Well Can DNA Rupture DNA? Shearing and Unzipping Forces inside DNA Nanostructures
title_short How Well Can DNA Rupture DNA? Shearing and Unzipping Forces inside DNA Nanostructures
title_sort how well can dna rupture dna? shearing and unzipping forces inside dna nanostructures
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044922/
https://www.ncbi.nlm.nih.gov/pubmed/30023776
http://dx.doi.org/10.1021/acsomega.7b01692
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