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Spectroscopic and molecular modeling studies of binding interaction between the new complex of yttrium and 1,10-phenanthroline derivatives with DNA and BSA

In this study, the 4,9 diazafluoren-9-one ligand and [Y(Daf)(2)Cl(3).OH(2)] complex were synthesized. The interaction of this complex with DNA and bovine serum albumin (BSA) was investigated by UV-vis and fluorescence spectroscopy. The molecular docking method was used to confirm the experimental re...

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Autores principales: Khorshidi, Mahsa, Asadpour, Saeid, Aramesh-Boroujeni, Zahra, Kooravand, Masoumeh, Mobini Dehkordi, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10483121/
https://www.ncbi.nlm.nih.gov/pubmed/37693170
http://dx.doi.org/10.3389/fchem.2023.1231504
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author Khorshidi, Mahsa
Asadpour, Saeid
Aramesh-Boroujeni, Zahra
Kooravand, Masoumeh
Mobini Dehkordi, Maryam
author_facet Khorshidi, Mahsa
Asadpour, Saeid
Aramesh-Boroujeni, Zahra
Kooravand, Masoumeh
Mobini Dehkordi, Maryam
author_sort Khorshidi, Mahsa
collection PubMed
description In this study, the 4,9 diazafluoren-9-one ligand and [Y(Daf)(2)Cl(3).OH(2)] complex were synthesized. The interaction of this complex with DNA and bovine serum albumin (BSA) was investigated by UV-vis and fluorescence spectroscopy. The molecular docking method was used to confirm the experimental results, investigate the type of interaction, and determine the binding site. The binding constant and Stern–Volmer constant were calculated using spectroscopy techniques. The binding constant of the Y-complex with DNA and BSA obtained using the UV-vis technique was 1.61 × 10(5) M(−1) and 0.49 × 10(5) M(−1), while that obtained using the fluorescence method was 3.39 × 10(5) M(−1) and 3.63 × 10(5) M(−1), respectively. The results of experimental and theoretical data showed that the interaction between the yttrium complex and DNA and BSA is driven by the hydrogen bond and van der Waals interaction, respectively. The yttrium complex communicates with DNA via the groove interaction. This complex has high binding energy with bovine serum albumin. In addition, the molecular docking results showed that the complex binds to the IIA subdomain of BSA (site I). Finally, anticancer activity of the yttrium complex was studied on MCF-7 and A549 cell lines by using the MTT method. The IC(50) values obtained showed that the yttrium complex possesses anticancer activity.
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spelling pubmed-104831212023-09-08 Spectroscopic and molecular modeling studies of binding interaction between the new complex of yttrium and 1,10-phenanthroline derivatives with DNA and BSA Khorshidi, Mahsa Asadpour, Saeid Aramesh-Boroujeni, Zahra Kooravand, Masoumeh Mobini Dehkordi, Maryam Front Chem Chemistry In this study, the 4,9 diazafluoren-9-one ligand and [Y(Daf)(2)Cl(3).OH(2)] complex were synthesized. The interaction of this complex with DNA and bovine serum albumin (BSA) was investigated by UV-vis and fluorescence spectroscopy. The molecular docking method was used to confirm the experimental results, investigate the type of interaction, and determine the binding site. The binding constant and Stern–Volmer constant were calculated using spectroscopy techniques. The binding constant of the Y-complex with DNA and BSA obtained using the UV-vis technique was 1.61 × 10(5) M(−1) and 0.49 × 10(5) M(−1), while that obtained using the fluorescence method was 3.39 × 10(5) M(−1) and 3.63 × 10(5) M(−1), respectively. The results of experimental and theoretical data showed that the interaction between the yttrium complex and DNA and BSA is driven by the hydrogen bond and van der Waals interaction, respectively. The yttrium complex communicates with DNA via the groove interaction. This complex has high binding energy with bovine serum albumin. In addition, the molecular docking results showed that the complex binds to the IIA subdomain of BSA (site I). Finally, anticancer activity of the yttrium complex was studied on MCF-7 and A549 cell lines by using the MTT method. The IC(50) values obtained showed that the yttrium complex possesses anticancer activity. Frontiers Media S.A. 2023-08-24 /pmc/articles/PMC10483121/ /pubmed/37693170 http://dx.doi.org/10.3389/fchem.2023.1231504 Text en Copyright © 2023 Khorshidi, Asadpour, Aramesh-Boroujeni, Kooravand and Mobini Dehkordi. https://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
Khorshidi, Mahsa
Asadpour, Saeid
Aramesh-Boroujeni, Zahra
Kooravand, Masoumeh
Mobini Dehkordi, Maryam
Spectroscopic and molecular modeling studies of binding interaction between the new complex of yttrium and 1,10-phenanthroline derivatives with DNA and BSA
title Spectroscopic and molecular modeling studies of binding interaction between the new complex of yttrium and 1,10-phenanthroline derivatives with DNA and BSA
title_full Spectroscopic and molecular modeling studies of binding interaction between the new complex of yttrium and 1,10-phenanthroline derivatives with DNA and BSA
title_fullStr Spectroscopic and molecular modeling studies of binding interaction between the new complex of yttrium and 1,10-phenanthroline derivatives with DNA and BSA
title_full_unstemmed Spectroscopic and molecular modeling studies of binding interaction between the new complex of yttrium and 1,10-phenanthroline derivatives with DNA and BSA
title_short Spectroscopic and molecular modeling studies of binding interaction between the new complex of yttrium and 1,10-phenanthroline derivatives with DNA and BSA
title_sort spectroscopic and molecular modeling studies of binding interaction between the new complex of yttrium and 1,10-phenanthroline derivatives with dna and bsa
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10483121/
https://www.ncbi.nlm.nih.gov/pubmed/37693170
http://dx.doi.org/10.3389/fchem.2023.1231504
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