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The Relation Between Position and Chemical Composition of Bis‐Indole Substituents Determines Their Interactions with G‐Quadruplex DNA
G‐quadruplex (G4) DNA structures are linked to fundamental biological processes and human diseases, which has triggered the development of compounds that affect these DNA structures. However, more knowledge is needed about how small molecules interact with G4 DNA structures. This study describes the...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497243/ https://www.ncbi.nlm.nih.gov/pubmed/32187406 http://dx.doi.org/10.1002/chem.202000579 |
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author | Prasad, Bagineni Das, Rabindra Nath Jamroskovic, Jan Kumar, Rajendra Hedenström, Mattias Sabouri, Nasim Chorell, Erik |
author_facet | Prasad, Bagineni Das, Rabindra Nath Jamroskovic, Jan Kumar, Rajendra Hedenström, Mattias Sabouri, Nasim Chorell, Erik |
author_sort | Prasad, Bagineni |
collection | PubMed |
description | G‐quadruplex (G4) DNA structures are linked to fundamental biological processes and human diseases, which has triggered the development of compounds that affect these DNA structures. However, more knowledge is needed about how small molecules interact with G4 DNA structures. This study describes the development of a new class of bis‐indoles (3,3‐diindolyl‐methyl derivatives) and detailed studies of how they interact with G4 DNA using orthogonal assays, biophysical techniques, and computational studies. This revealed compounds that strongly bind and stabilize G4 DNA structures, and detailed binding interactions which for example, show that charge variance can play a key role in G4 DNA binding. Furthermore, the structure–activity relationships generated opened the possibilities to replace or introduce new substituents on the core structure, which is of key importance to optimize compound properties or introduce probes to further expand the possibilities of these compounds as tailored research tools to study G4 biology. |
format | Online Article Text |
id | pubmed-7497243 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74972432020-09-25 The Relation Between Position and Chemical Composition of Bis‐Indole Substituents Determines Their Interactions with G‐Quadruplex DNA Prasad, Bagineni Das, Rabindra Nath Jamroskovic, Jan Kumar, Rajendra Hedenström, Mattias Sabouri, Nasim Chorell, Erik Chemistry Full Papers G‐quadruplex (G4) DNA structures are linked to fundamental biological processes and human diseases, which has triggered the development of compounds that affect these DNA structures. However, more knowledge is needed about how small molecules interact with G4 DNA structures. This study describes the development of a new class of bis‐indoles (3,3‐diindolyl‐methyl derivatives) and detailed studies of how they interact with G4 DNA using orthogonal assays, biophysical techniques, and computational studies. This revealed compounds that strongly bind and stabilize G4 DNA structures, and detailed binding interactions which for example, show that charge variance can play a key role in G4 DNA binding. Furthermore, the structure–activity relationships generated opened the possibilities to replace or introduce new substituents on the core structure, which is of key importance to optimize compound properties or introduce probes to further expand the possibilities of these compounds as tailored research tools to study G4 biology. John Wiley and Sons Inc. 2020-07-03 2020-08-03 /pmc/articles/PMC7497243/ /pubmed/32187406 http://dx.doi.org/10.1002/chem.202000579 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers Prasad, Bagineni Das, Rabindra Nath Jamroskovic, Jan Kumar, Rajendra Hedenström, Mattias Sabouri, Nasim Chorell, Erik The Relation Between Position and Chemical Composition of Bis‐Indole Substituents Determines Their Interactions with G‐Quadruplex DNA |
title | The Relation Between Position and Chemical Composition of Bis‐Indole Substituents Determines Their Interactions with G‐Quadruplex DNA |
title_full | The Relation Between Position and Chemical Composition of Bis‐Indole Substituents Determines Their Interactions with G‐Quadruplex DNA |
title_fullStr | The Relation Between Position and Chemical Composition of Bis‐Indole Substituents Determines Their Interactions with G‐Quadruplex DNA |
title_full_unstemmed | The Relation Between Position and Chemical Composition of Bis‐Indole Substituents Determines Their Interactions with G‐Quadruplex DNA |
title_short | The Relation Between Position and Chemical Composition of Bis‐Indole Substituents Determines Their Interactions with G‐Quadruplex DNA |
title_sort | relation between position and chemical composition of bis‐indole substituents determines their interactions with g‐quadruplex dna |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497243/ https://www.ncbi.nlm.nih.gov/pubmed/32187406 http://dx.doi.org/10.1002/chem.202000579 |
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