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Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies

Recently, we studied glucose-nucleobase pairs, a binding motif found in aminoglycoside–RNA recognition. DNA duplexes with glucose as a nucleobase were able to hybridize and were selective for purines. They were less stable than natural DNA but still fit well on regular B-DNA. These results opened up...

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Autores principales: Vengut-Climent, Empar, Peñalver, Pablo, Lucas, Ricardo, Gómez-Pinto, Irene, Aviñó, Anna, Muro-Pastor, Alicia M., Galbis, Elsa, de Paz, M. Violante, Fonseca Guerra, Célia, Bickelhaupt, F. Matthias, Eritja, Ramón, González, Carlos, Morales, Juan Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934746/
https://www.ncbi.nlm.nih.gov/pubmed/29780486
http://dx.doi.org/10.1039/c7sc04850e
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author Vengut-Climent, Empar
Peñalver, Pablo
Lucas, Ricardo
Gómez-Pinto, Irene
Aviñó, Anna
Muro-Pastor, Alicia M.
Galbis, Elsa
de Paz, M. Violante
Fonseca Guerra, Célia
Bickelhaupt, F. Matthias
Eritja, Ramón
González, Carlos
Morales, Juan Carlos
author_facet Vengut-Climent, Empar
Peñalver, Pablo
Lucas, Ricardo
Gómez-Pinto, Irene
Aviñó, Anna
Muro-Pastor, Alicia M.
Galbis, Elsa
de Paz, M. Violante
Fonseca Guerra, Célia
Bickelhaupt, F. Matthias
Eritja, Ramón
González, Carlos
Morales, Juan Carlos
author_sort Vengut-Climent, Empar
collection PubMed
description Recently, we studied glucose-nucleobase pairs, a binding motif found in aminoglycoside–RNA recognition. DNA duplexes with glucose as a nucleobase were able to hybridize and were selective for purines. They were less stable than natural DNA but still fit well on regular B-DNA. These results opened up the possible use of glucose as a non-aromatic DNA base mimic. Here, we have studied the incorporation and thermal stability of glucose with different types of anchoring units and alternative apolar sugar-nucleobase pairs. When we explored butanetriol instead of glycerol as a wider anchoring unit, we did not gain duplex thermal stability. This result confirmed the necessity of a more conformationally restricted linker to increase the overall duplex stability. Permethylated glucose-nucleobase pairs showed similar stability to glucoside-nucleobase pairs but no selectivity for a specific nucleobase, possibly due to the absence of hydrogen bonds between them. The three-dimensional structure of the duplex solved by NMR located both, the hydrophobic permethylated glucose and the nucleobase, inside the DNA helix as in the case of glucose-nucleobase pairs. Quantum chemical calculations on glucose-nucleobase pairs indicate that the attachment of the sugar to the DNA skeleton through the OH1 or OH4 positions yields the highest binding energies. Moreover, glucose was very selective for guanine when attached through OH1 or OH4 to the DNA. Finally, we examined DNA polymerase insertion of nucleotides in front of the saccharide unit. KF(–) polymerase from E. coli inserted A and G opposite glc and 6dglc with low efficiency but notable selectivity. It is even capable of extending the new pair although its efficiency depended on the DNA sequence. In contrast, Bst 2.0, SIII and BIOTAQ™ DNA polymerases seem to display a loop-out mechanism possibly due to the flexible glycerol linker used instead of deoxyribose.
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spelling pubmed-59347462018-05-18 Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies Vengut-Climent, Empar Peñalver, Pablo Lucas, Ricardo Gómez-Pinto, Irene Aviñó, Anna Muro-Pastor, Alicia M. Galbis, Elsa de Paz, M. Violante Fonseca Guerra, Célia Bickelhaupt, F. Matthias Eritja, Ramón González, Carlos Morales, Juan Carlos Chem Sci Chemistry Recently, we studied glucose-nucleobase pairs, a binding motif found in aminoglycoside–RNA recognition. DNA duplexes with glucose as a nucleobase were able to hybridize and were selective for purines. They were less stable than natural DNA but still fit well on regular B-DNA. These results opened up the possible use of glucose as a non-aromatic DNA base mimic. Here, we have studied the incorporation and thermal stability of glucose with different types of anchoring units and alternative apolar sugar-nucleobase pairs. When we explored butanetriol instead of glycerol as a wider anchoring unit, we did not gain duplex thermal stability. This result confirmed the necessity of a more conformationally restricted linker to increase the overall duplex stability. Permethylated glucose-nucleobase pairs showed similar stability to glucoside-nucleobase pairs but no selectivity for a specific nucleobase, possibly due to the absence of hydrogen bonds between them. The three-dimensional structure of the duplex solved by NMR located both, the hydrophobic permethylated glucose and the nucleobase, inside the DNA helix as in the case of glucose-nucleobase pairs. Quantum chemical calculations on glucose-nucleobase pairs indicate that the attachment of the sugar to the DNA skeleton through the OH1 or OH4 positions yields the highest binding energies. Moreover, glucose was very selective for guanine when attached through OH1 or OH4 to the DNA. Finally, we examined DNA polymerase insertion of nucleotides in front of the saccharide unit. KF(–) polymerase from E. coli inserted A and G opposite glc and 6dglc with low efficiency but notable selectivity. It is even capable of extending the new pair although its efficiency depended on the DNA sequence. In contrast, Bst 2.0, SIII and BIOTAQ™ DNA polymerases seem to display a loop-out mechanism possibly due to the flexible glycerol linker used instead of deoxyribose. Royal Society of Chemistry 2018-03-05 /pmc/articles/PMC5934746/ /pubmed/29780486 http://dx.doi.org/10.1039/c7sc04850e Text en This journal is © The Royal Society of Chemistry 2018 http://creativecommons.org/licenses/by/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0)
spellingShingle Chemistry
Vengut-Climent, Empar
Peñalver, Pablo
Lucas, Ricardo
Gómez-Pinto, Irene
Aviñó, Anna
Muro-Pastor, Alicia M.
Galbis, Elsa
de Paz, M. Violante
Fonseca Guerra, Célia
Bickelhaupt, F. Matthias
Eritja, Ramón
González, Carlos
Morales, Juan Carlos
Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies
title Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies
title_full Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies
title_fullStr Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies
title_full_unstemmed Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies
title_short Glucose-nucleobase pairs within DNA: impact of hydrophobicity, alternative linking unit and DNA polymerase nucleotide insertion studies
title_sort glucose-nucleobase pairs within dna: impact of hydrophobicity, alternative linking unit and dna polymerase nucleotide insertion studies
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934746/
https://www.ncbi.nlm.nih.gov/pubmed/29780486
http://dx.doi.org/10.1039/c7sc04850e
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