The influence of the metal cations and microhydration on the reaction trajectory of the N3 ↔ O2 thymine proton transfer: Quantum mechanical study
This study involves the intramolecular proton transfer (PT) process on a thymine nucleobase between N3 and O2 atoms. We explore a mechanism for the PT assisted by hexacoordinated divalent metals cations, namely Mg2+, Zn2+, and Hg2+. Our results point out that this reaction corresponds to a two‐stage...
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| Vydáno v: | Journal of computational chemistry Ročník 38; číslo 31; s. 2680 - 2692 |
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| Médium: | Journal Article |
| Jazyk: | angličtina |
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05.12.2017
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| ISSN: | 0192-8651, 1096-987X, 1096-987X |
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| Abstract | This study involves the intramolecular proton transfer (PT) process on a thymine nucleobase between N3 and O2 atoms. We explore a mechanism for the PT assisted by hexacoordinated divalent metals cations, namely Mg2+, Zn2+, and Hg2+. Our results point out that this reaction corresponds to a two‐stage process. The first involves the PT from one of the aqua ligands toward O2. The implications of this stage are the formation of a hydroxo anion bound to the metal center and a positively charged thymine. To proceed to the second stage, a structural change is needed to allow the negatively charged hydroxo ligand to the N3 proton, which represents the final product of the PT reaction. In the presence of the selected hexaaqua cations, the activation barrier is at most 8 kcal/mol. © 2017 Wiley Periodicals, Inc.
Intramolecular proton transfer (PT) process on thymine nucleobase between N3 and O2 atoms is explored in presence of hexacoordinated divalent metals cations Mg2+, Zn2+, and Hg2+. This PT proceeds as a two stages process. The first step involves the PT from one of the aqua ligands toward O2. The second stage is connected with the N3‐proton ion. In the presence of the hexaaqua‐cations, the activation barrier is at most 8 kcal/mol. |
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| AbstractList | This study involves the intramolecular proton transfer (PT) process on a thymine nucleobase between N3 and O2 atoms. We explore a mechanism for the PT assisted by hexacoordinated divalent metals cations, namely Mg2+, Zn2+, and Hg2+. Our results point out that this reaction corresponds to a two‐stage process. The first involves the PT from one of the aqua ligands toward O2. The implications of this stage are the formation of a hydroxo anion bound to the metal center and a positively charged thymine. To proceed to the second stage, a structural change is needed to allow the negatively charged hydroxo ligand to the N3 proton, which represents the final product of the PT reaction. In the presence of the selected hexaaqua cations, the activation barrier is at most 8 kcal/mol. © 2017 Wiley Periodicals, Inc.
Intramolecular proton transfer (PT) process on thymine nucleobase between N3 and O2 atoms is explored in presence of hexacoordinated divalent metals cations Mg2+, Zn2+, and Hg2+. This PT proceeds as a two stages process. The first step involves the PT from one of the aqua ligands toward O2. The second stage is connected with the N3‐proton ion. In the presence of the hexaaqua‐cations, the activation barrier is at most 8 kcal/mol. This study involves the intramolecular proton transfer (PT) process on a thymine nucleobase between N3 and O2 atoms. We explore a mechanism for the PT assisted by hexacoordinated divalent metals cations, namely Mg2+ , Zn2+ , and Hg2+ . Our results point out that this reaction corresponds to a two-stage process. The first involves the PT from one of the aqua ligands toward O2. The implications of this stage are the formation of a hydroxo anion bound to the metal center and a positively charged thymine. To proceed to the second stage, a structural change is needed to allow the negatively charged hydroxo ligand to abstract the N3 proton, which represents the final product of the PT reaction. In the presence of the selected hexaaqua cations, the activation barrier is at most 8 kcal/mol. © 2017 Wiley Periodicals, Inc.This study involves the intramolecular proton transfer (PT) process on a thymine nucleobase between N3 and O2 atoms. We explore a mechanism for the PT assisted by hexacoordinated divalent metals cations, namely Mg2+ , Zn2+ , and Hg2+ . Our results point out that this reaction corresponds to a two-stage process. The first involves the PT from one of the aqua ligands toward O2. The implications of this stage are the formation of a hydroxo anion bound to the metal center and a positively charged thymine. To proceed to the second stage, a structural change is needed to allow the negatively charged hydroxo ligand to abstract the N3 proton, which represents the final product of the PT reaction. In the presence of the selected hexaaqua cations, the activation barrier is at most 8 kcal/mol. © 2017 Wiley Periodicals, Inc. This study involves the intramolecular proton transfer (PT) process on a thymine nucleobase between N3 and O2 atoms. We explore a mechanism for the PT assisted by hexacoordinated divalent metals cations, namely Mg 2+ , Zn 2+ , and Hg 2+ . Our results point out that this reaction corresponds to a two‐stage process. The first involves the PT from one of the aqua ligands toward O2. The implications of this stage are the formation of a hydroxo anion bound to the metal center and a positively charged thymine. To proceed to the second stage, a structural change is needed to allow the negatively charged hydroxo ligand to abstract the N3 proton, which represents the final product of the PT reaction. In the presence of the selected hexaaqua cations, the activation barrier is at most 8 kcal/mol. © 2017 Wiley Periodicals, Inc. This study involves the intramolecular proton transfer (PT) process on a thymine nucleobase between N3 and O2 atoms. We explore a mechanism for the PT assisted by hexacoordinated divalent metals cations, namely Mg , Zn , and Hg . Our results point out that this reaction corresponds to a two-stage process. The first involves the PT from one of the aqua ligands toward O2. The implications of this stage are the formation of a hydroxo anion bound to the metal center and a positively charged thymine. To proceed to the second stage, a structural change is needed to allow the negatively charged hydroxo ligand to abstract the N3 proton, which represents the final product of the PT reaction. In the presence of the selected hexaaqua cations, the activation barrier is at most 8 kcal/mol. © 2017 Wiley Periodicals, Inc. This study involves the intramolecular proton transfer (PT) process on a thymine nucleobase between N3 and O2 atoms. We explore a mechanism for the PT assisted by hexacoordinated divalent metals cations, namely Mg2+, Zn2+, and Hg2+. Our results point out that this reaction corresponds to a two-stage process. The first involves the PT from one of the aqua ligands toward O2. The implications of this stage are the formation of a hydroxo anion bound to the metal center and a positively charged thymine. To proceed to the second stage, a structural change is needed to allow the negatively charged hydroxo ligand to abstract the N3 proton, which represents the final product of the PT reaction. In the presence of the selected hexaaqua cations, the activation barrier is at most 8 kcal/mol. © 2017 Wiley Periodicals, Inc. |
| Author | Michalak, Artur Murray, Jane S Miranda, Sebastian Gutiérrez‐Oliva, Soledad Šebesta, Filip Burda, Jaroslav V Toro‐Labbé, Alejandro Brela, Mateusz Z Diaz, Silvia |
| Author_xml | – sequence: 1 givenname: Filip surname: Šebesta fullname: Šebesta, Filip organization: Charles University, Ke Karlovu 3 – sequence: 2 givenname: Mateusz Z surname: Brela fullname: Brela, Mateusz Z organization: Faculty of Chemistry, Jagiellonian University, R. Ingardena 3 – sequence: 3 givenname: Silvia surname: Diaz fullname: Diaz, Silvia organization: Laboratorio de Química Teórica Computacional (QTC), Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Casilla 306, Correo 22 – sequence: 4 givenname: Sebastian surname: Miranda fullname: Miranda, Sebastian organization: Laboratorio de Química Teórica Computacional (QTC), Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Casilla 306, Correo 22 – sequence: 5 givenname: Jane S surname: Murray fullname: Murray, Jane S organization: University of New Orleans – sequence: 6 givenname: Soledad surname: Gutiérrez‐Oliva fullname: Gutiérrez‐Oliva, Soledad organization: Laboratorio de Química Teórica Computacional (QTC), Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Casilla 306, Correo 22 – sequence: 7 givenname: Alejandro surname: Toro‐Labbé fullname: Toro‐Labbé, Alejandro organization: Laboratorio de Química Teórica Computacional (QTC), Facultad de Química, Pontificia Universidad Católica de Chile, Vicuña Mackenna 4860, Casilla 306, Correo 22 – sequence: 8 givenname: Artur orcidid: 0000-0003-1408-5474 surname: Michalak fullname: Michalak, Artur organization: Faculty of Chemistry, Jagiellonian University, R. Ingardena 3 – sequence: 9 givenname: Jaroslav V orcidid: 0000-0001-9909-8797 surname: Burda fullname: Burda, Jaroslav V email: burda@karlov.mff.cuni.cz organization: Charles University, Ke Karlovu 3 |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28925001$$D View this record in MEDLINE/PubMed |
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| Keywords | reaction coordinate proton transfer DFT chemical potential thymine |
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| Snippet | This study involves the intramolecular proton transfer (PT) process on a thymine nucleobase between N3 and O2 atoms. We explore a mechanism for the PT assisted... |
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| SubjectTerms | Cations chemical potential Computational chemistry DFT Ions Ligands Mercury (metal) Molecular chemistry Nuclei proton transfer Protons Quantum mechanics reaction coordinate Thymine |
| Title | The influence of the metal cations and microhydration on the reaction trajectory of the N3 ↔ O2 thymine proton transfer: Quantum mechanical study |
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