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The association constant of 5′,8-cyclo-2′-deoxyguanosine with cytidine
The association of 5′,8-cyclo-2′-deoxyguanosine (cdG), a DNA tandem lesion, with its complementary base cytosine has been studied by voltammetry and NMR in chloroform, using properly silylated derivatives of the two nucleobases for increasing their solubilities. Both voltammetric data and NMR titrat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376000/ https://www.ncbi.nlm.nih.gov/pubmed/25870853 http://dx.doi.org/10.3389/fchem.2015.00022 |
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author | Capobianco, Amedeo Caruso, Tonino Fusco, Sandra Terzidis, Michael A. Masi, Annalisa Chatgilialoglu, Chryssostomos Peluso, Andrea |
author_facet | Capobianco, Amedeo Caruso, Tonino Fusco, Sandra Terzidis, Michael A. Masi, Annalisa Chatgilialoglu, Chryssostomos Peluso, Andrea |
author_sort | Capobianco, Amedeo |
collection | PubMed |
description | The association of 5′,8-cyclo-2′-deoxyguanosine (cdG), a DNA tandem lesion, with its complementary base cytosine has been studied by voltammetry and NMR in chloroform, using properly silylated derivatives of the two nucleobases for increasing their solubilities. Both voltammetric data and NMR titrations indicated that the Watson-Crick complex of cytidine with cdG is weaker than that with guanosine, the difference being approximately of one order of magnitude between the two association constants. |
format | Online Article Text |
id | pubmed-4376000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-43760002015-04-13 The association constant of 5′,8-cyclo-2′-deoxyguanosine with cytidine Capobianco, Amedeo Caruso, Tonino Fusco, Sandra Terzidis, Michael A. Masi, Annalisa Chatgilialoglu, Chryssostomos Peluso, Andrea Front Chem Chemistry The association of 5′,8-cyclo-2′-deoxyguanosine (cdG), a DNA tandem lesion, with its complementary base cytosine has been studied by voltammetry and NMR in chloroform, using properly silylated derivatives of the two nucleobases for increasing their solubilities. Both voltammetric data and NMR titrations indicated that the Watson-Crick complex of cytidine with cdG is weaker than that with guanosine, the difference being approximately of one order of magnitude between the two association constants. Frontiers Media S.A. 2015-03-27 /pmc/articles/PMC4376000/ /pubmed/25870853 http://dx.doi.org/10.3389/fchem.2015.00022 Text en Copyright © 2015 Capobianco, Caruso, Fusco, Terzidis, Masi, Chatgilialoglu and Peluso. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Capobianco, Amedeo Caruso, Tonino Fusco, Sandra Terzidis, Michael A. Masi, Annalisa Chatgilialoglu, Chryssostomos Peluso, Andrea The association constant of 5′,8-cyclo-2′-deoxyguanosine with cytidine |
title | The association constant of 5′,8-cyclo-2′-deoxyguanosine with cytidine |
title_full | The association constant of 5′,8-cyclo-2′-deoxyguanosine with cytidine |
title_fullStr | The association constant of 5′,8-cyclo-2′-deoxyguanosine with cytidine |
title_full_unstemmed | The association constant of 5′,8-cyclo-2′-deoxyguanosine with cytidine |
title_short | The association constant of 5′,8-cyclo-2′-deoxyguanosine with cytidine |
title_sort | association constant of 5′,8-cyclo-2′-deoxyguanosine with cytidine |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376000/ https://www.ncbi.nlm.nih.gov/pubmed/25870853 http://dx.doi.org/10.3389/fchem.2015.00022 |
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