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Gel-Free Tools for Quick and Simple Screening of Anti-Topoisomerase 1 Compounds

With the increasing need for effective compounds against cancer or pathogen-borne diseases, the development of new tools to investigate the enzymatic activity of biomarkers is necessary. Among these biomarkers are DNA topoisomerases, which are key enzymes that modify DNA and regulate DNA topology du...

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Autores principales: Keller, Josephine Geertsen, Petersen, Kamilla Vandsø, Mizielinski, Karol, Thiesen, Celine, Bjergbæk, Lotte, Reguera, Rosa M., Pérez-Pertejo, Yolanda, Balaña-Fouce, Rafael, Trejo, Angela, Masdeu, Carme, Alonso, Concepcion, Knudsen, Birgitta R., Tesauro, Cinzia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221459/
https://www.ncbi.nlm.nih.gov/pubmed/37242440
http://dx.doi.org/10.3390/ph16050657
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author Keller, Josephine Geertsen
Petersen, Kamilla Vandsø
Mizielinski, Karol
Thiesen, Celine
Bjergbæk, Lotte
Reguera, Rosa M.
Pérez-Pertejo, Yolanda
Balaña-Fouce, Rafael
Trejo, Angela
Masdeu, Carme
Alonso, Concepcion
Knudsen, Birgitta R.
Tesauro, Cinzia
author_facet Keller, Josephine Geertsen
Petersen, Kamilla Vandsø
Mizielinski, Karol
Thiesen, Celine
Bjergbæk, Lotte
Reguera, Rosa M.
Pérez-Pertejo, Yolanda
Balaña-Fouce, Rafael
Trejo, Angela
Masdeu, Carme
Alonso, Concepcion
Knudsen, Birgitta R.
Tesauro, Cinzia
author_sort Keller, Josephine Geertsen
collection PubMed
description With the increasing need for effective compounds against cancer or pathogen-borne diseases, the development of new tools to investigate the enzymatic activity of biomarkers is necessary. Among these biomarkers are DNA topoisomerases, which are key enzymes that modify DNA and regulate DNA topology during cellular processes. Over the years, libraries of natural and synthetic small-molecule compounds have been extensively investigated as potential anti-cancer, anti-bacterial, or anti-parasitic drugs targeting topoisomerases. However, the current tools for measuring the potential inhibition of topoisomerase activity are time consuming and not easily adaptable outside specialized laboratories. Here, we present rolling circle amplification-based methods that provide fast and easy readouts for screening of compounds against type 1 topoisomerases. Specific assays for the investigation of the potential inhibition of eukaryotic, viral, or bacterial type 1 topoisomerase activity were developed, using human topoisomerase 1, Leishmania donovani topoisomerase 1, monkeypox virus topoisomerase 1, and Mycobacterium smegmatis topoisomerase 1 as model enzymes. The presented tools proved to be sensitive and directly quantitative, paving the way for new diagnostic and drug screening protocols in research and clinical settings.
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spelling pubmed-102214592023-05-28 Gel-Free Tools for Quick and Simple Screening of Anti-Topoisomerase 1 Compounds Keller, Josephine Geertsen Petersen, Kamilla Vandsø Mizielinski, Karol Thiesen, Celine Bjergbæk, Lotte Reguera, Rosa M. Pérez-Pertejo, Yolanda Balaña-Fouce, Rafael Trejo, Angela Masdeu, Carme Alonso, Concepcion Knudsen, Birgitta R. Tesauro, Cinzia Pharmaceuticals (Basel) Article With the increasing need for effective compounds against cancer or pathogen-borne diseases, the development of new tools to investigate the enzymatic activity of biomarkers is necessary. Among these biomarkers are DNA topoisomerases, which are key enzymes that modify DNA and regulate DNA topology during cellular processes. Over the years, libraries of natural and synthetic small-molecule compounds have been extensively investigated as potential anti-cancer, anti-bacterial, or anti-parasitic drugs targeting topoisomerases. However, the current tools for measuring the potential inhibition of topoisomerase activity are time consuming and not easily adaptable outside specialized laboratories. Here, we present rolling circle amplification-based methods that provide fast and easy readouts for screening of compounds against type 1 topoisomerases. Specific assays for the investigation of the potential inhibition of eukaryotic, viral, or bacterial type 1 topoisomerase activity were developed, using human topoisomerase 1, Leishmania donovani topoisomerase 1, monkeypox virus topoisomerase 1, and Mycobacterium smegmatis topoisomerase 1 as model enzymes. The presented tools proved to be sensitive and directly quantitative, paving the way for new diagnostic and drug screening protocols in research and clinical settings. MDPI 2023-04-27 /pmc/articles/PMC10221459/ /pubmed/37242440 http://dx.doi.org/10.3390/ph16050657 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Keller, Josephine Geertsen
Petersen, Kamilla Vandsø
Mizielinski, Karol
Thiesen, Celine
Bjergbæk, Lotte
Reguera, Rosa M.
Pérez-Pertejo, Yolanda
Balaña-Fouce, Rafael
Trejo, Angela
Masdeu, Carme
Alonso, Concepcion
Knudsen, Birgitta R.
Tesauro, Cinzia
Gel-Free Tools for Quick and Simple Screening of Anti-Topoisomerase 1 Compounds
title Gel-Free Tools for Quick and Simple Screening of Anti-Topoisomerase 1 Compounds
title_full Gel-Free Tools for Quick and Simple Screening of Anti-Topoisomerase 1 Compounds
title_fullStr Gel-Free Tools for Quick and Simple Screening of Anti-Topoisomerase 1 Compounds
title_full_unstemmed Gel-Free Tools for Quick and Simple Screening of Anti-Topoisomerase 1 Compounds
title_short Gel-Free Tools for Quick and Simple Screening of Anti-Topoisomerase 1 Compounds
title_sort gel-free tools for quick and simple screening of anti-topoisomerase 1 compounds
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10221459/
https://www.ncbi.nlm.nih.gov/pubmed/37242440
http://dx.doi.org/10.3390/ph16050657
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