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Sequence dependence of electron-induced DNA strand breakage revealed by DNA nanoarrays

The electronic structure of DNA is determined by its nucleotide sequence, which is for instance exploited in molecular electronics. Here we demonstrate that also the DNA strand breakage induced by low-energy electrons (18 eV) depends on the nucleotide sequence. To determine the absolute cross sectio...

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Autores principales: Keller, Adrian, Rackwitz, Jenny, Cauët, Emilie, Liévin, Jacques, Körzdörfer, Thomas, Rotaru, Alexandru, Gothelf, Kurt V., Besenbacher, Flemming, Bald, Ilko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260214/
https://www.ncbi.nlm.nih.gov/pubmed/25487346
http://dx.doi.org/10.1038/srep07391
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author Keller, Adrian
Rackwitz, Jenny
Cauët, Emilie
Liévin, Jacques
Körzdörfer, Thomas
Rotaru, Alexandru
Gothelf, Kurt V.
Besenbacher, Flemming
Bald, Ilko
author_facet Keller, Adrian
Rackwitz, Jenny
Cauët, Emilie
Liévin, Jacques
Körzdörfer, Thomas
Rotaru, Alexandru
Gothelf, Kurt V.
Besenbacher, Flemming
Bald, Ilko
author_sort Keller, Adrian
collection PubMed
description The electronic structure of DNA is determined by its nucleotide sequence, which is for instance exploited in molecular electronics. Here we demonstrate that also the DNA strand breakage induced by low-energy electrons (18 eV) depends on the nucleotide sequence. To determine the absolute cross sections for electron induced single strand breaks in specific 13 mer oligonucleotides we used atomic force microscopy analysis of DNA origami based DNA nanoarrays. We investigated the DNA sequences 5′-TT(XYX)(3)TT with X = A, G, C and Y = T, BrU 5-bromouracil and found absolute strand break cross sections between 2.66 · 10(−14) cm(2) and 7.06 · 10(−14) cm(2). The highest cross section was found for 5′-TT(ATA)(3)TT and 5′-TT(ABrUA)(3)TT, respectively. BrU is a radiosensitizer, which was discussed to be used in cancer radiation therapy. The replacement of T by BrU into the investigated DNA sequences leads to a slight increase of the absolute strand break cross sections resulting in sequence-dependent enhancement factors between 1.14 and 1.66. Nevertheless, the variation of strand break cross sections due to the specific nucleotide sequence is considerably higher. Thus, the present results suggest the development of targeted radiosensitizers for cancer radiation therapy.
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spelling pubmed-42602142014-12-15 Sequence dependence of electron-induced DNA strand breakage revealed by DNA nanoarrays Keller, Adrian Rackwitz, Jenny Cauët, Emilie Liévin, Jacques Körzdörfer, Thomas Rotaru, Alexandru Gothelf, Kurt V. Besenbacher, Flemming Bald, Ilko Sci Rep Article The electronic structure of DNA is determined by its nucleotide sequence, which is for instance exploited in molecular electronics. Here we demonstrate that also the DNA strand breakage induced by low-energy electrons (18 eV) depends on the nucleotide sequence. To determine the absolute cross sections for electron induced single strand breaks in specific 13 mer oligonucleotides we used atomic force microscopy analysis of DNA origami based DNA nanoarrays. We investigated the DNA sequences 5′-TT(XYX)(3)TT with X = A, G, C and Y = T, BrU 5-bromouracil and found absolute strand break cross sections between 2.66 · 10(−14) cm(2) and 7.06 · 10(−14) cm(2). The highest cross section was found for 5′-TT(ATA)(3)TT and 5′-TT(ABrUA)(3)TT, respectively. BrU is a radiosensitizer, which was discussed to be used in cancer radiation therapy. The replacement of T by BrU into the investigated DNA sequences leads to a slight increase of the absolute strand break cross sections resulting in sequence-dependent enhancement factors between 1.14 and 1.66. Nevertheless, the variation of strand break cross sections due to the specific nucleotide sequence is considerably higher. Thus, the present results suggest the development of targeted radiosensitizers for cancer radiation therapy. Nature Publishing Group 2014-12-09 /pmc/articles/PMC4260214/ /pubmed/25487346 http://dx.doi.org/10.1038/srep07391 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder in order to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Article
Keller, Adrian
Rackwitz, Jenny
Cauët, Emilie
Liévin, Jacques
Körzdörfer, Thomas
Rotaru, Alexandru
Gothelf, Kurt V.
Besenbacher, Flemming
Bald, Ilko
Sequence dependence of electron-induced DNA strand breakage revealed by DNA nanoarrays
title Sequence dependence of electron-induced DNA strand breakage revealed by DNA nanoarrays
title_full Sequence dependence of electron-induced DNA strand breakage revealed by DNA nanoarrays
title_fullStr Sequence dependence of electron-induced DNA strand breakage revealed by DNA nanoarrays
title_full_unstemmed Sequence dependence of electron-induced DNA strand breakage revealed by DNA nanoarrays
title_short Sequence dependence of electron-induced DNA strand breakage revealed by DNA nanoarrays
title_sort sequence dependence of electron-induced dna strand breakage revealed by dna nanoarrays
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260214/
https://www.ncbi.nlm.nih.gov/pubmed/25487346
http://dx.doi.org/10.1038/srep07391
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