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TriplatinNC and Biomolecules: Building Models Based on Non-covalent Interactions

The class of polynuclear platinum(II) compounds have demonstrated a great interest because their high activity against cancer cells. Among these new compounds, the TriplatinNC also called AH78, demonstrated surprising antitumor activity, in some cases equivalent to cisplatin. It is well-known that c...

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Autores principales: Rosa, Nathália M. P., Ferreira, Frederico Henrique do C., Farrell, Nicholas P., Costa, Luiz Antônio S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558404/
https://www.ncbi.nlm.nih.gov/pubmed/31231629
http://dx.doi.org/10.3389/fchem.2019.00307
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author Rosa, Nathália M. P.
Ferreira, Frederico Henrique do C.
Farrell, Nicholas P.
Costa, Luiz Antônio S.
author_facet Rosa, Nathália M. P.
Ferreira, Frederico Henrique do C.
Farrell, Nicholas P.
Costa, Luiz Antônio S.
author_sort Rosa, Nathália M. P.
collection PubMed
description The class of polynuclear platinum(II) compounds have demonstrated a great interest because their high activity against cancer cells. Among these new compounds, the TriplatinNC also called AH78, demonstrated surprising antitumor activity, in some cases equivalent to cisplatin. It is well-known that complex charge +8 favors interaction with DNA and other biomolecules non-covalently, through the hydrogen bonds with phosphate and sulfate groups present in these structures. The hydrogen atoms of the amine interact with the oxygen atoms of the phosphate and sulfate groups present in the DNA strand and heparan sulfate, respectively. These interactions can cause significant twists in double helix and inhibit the activity of these biomolecules. The present investigation is an attempt to provide a benchmark theoretical study about TriplatinNC. We have described the non-covalent interactions through small reliable mimetic models. The non-covalent interactions were also evaluated on larger models containing DNA fractions with six nitrogenous base pairs (CGCGAA) and fractions of the disaccharide that makes the HS evaluated by the hybrid QM/MM ONIOM methodology.
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spelling pubmed-65584042019-06-21 TriplatinNC and Biomolecules: Building Models Based on Non-covalent Interactions Rosa, Nathália M. P. Ferreira, Frederico Henrique do C. Farrell, Nicholas P. Costa, Luiz Antônio S. Front Chem Chemistry The class of polynuclear platinum(II) compounds have demonstrated a great interest because their high activity against cancer cells. Among these new compounds, the TriplatinNC also called AH78, demonstrated surprising antitumor activity, in some cases equivalent to cisplatin. It is well-known that complex charge +8 favors interaction with DNA and other biomolecules non-covalently, through the hydrogen bonds with phosphate and sulfate groups present in these structures. The hydrogen atoms of the amine interact with the oxygen atoms of the phosphate and sulfate groups present in the DNA strand and heparan sulfate, respectively. These interactions can cause significant twists in double helix and inhibit the activity of these biomolecules. The present investigation is an attempt to provide a benchmark theoretical study about TriplatinNC. We have described the non-covalent interactions through small reliable mimetic models. The non-covalent interactions were also evaluated on larger models containing DNA fractions with six nitrogenous base pairs (CGCGAA) and fractions of the disaccharide that makes the HS evaluated by the hybrid QM/MM ONIOM methodology. Frontiers Media S.A. 2019-05-21 /pmc/articles/PMC6558404/ /pubmed/31231629 http://dx.doi.org/10.3389/fchem.2019.00307 Text en Copyright © 2019 Rosa, Ferreira, Farrell and Costa. 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) and the copyright owner(s) 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
Rosa, Nathália M. P.
Ferreira, Frederico Henrique do C.
Farrell, Nicholas P.
Costa, Luiz Antônio S.
TriplatinNC and Biomolecules: Building Models Based on Non-covalent Interactions
title TriplatinNC and Biomolecules: Building Models Based on Non-covalent Interactions
title_full TriplatinNC and Biomolecules: Building Models Based on Non-covalent Interactions
title_fullStr TriplatinNC and Biomolecules: Building Models Based on Non-covalent Interactions
title_full_unstemmed TriplatinNC and Biomolecules: Building Models Based on Non-covalent Interactions
title_short TriplatinNC and Biomolecules: Building Models Based on Non-covalent Interactions
title_sort triplatinnc and biomolecules: building models based on non-covalent interactions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558404/
https://www.ncbi.nlm.nih.gov/pubmed/31231629
http://dx.doi.org/10.3389/fchem.2019.00307
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