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Targeting L-Proline Uptake as New Strategy for Anti-chagas Drug Development
L-Proline is an important amino acid for the pathogenic protists belonging to Trypanosoma and Leishmania genera. In Trypanosoma cruzi, the etiological agent of Chagas disease, this amino acid is involved in fundamental biological processes such as ATP production, differentiation of the insect and in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477874/ https://www.ncbi.nlm.nih.gov/pubmed/33195007 http://dx.doi.org/10.3389/fchem.2020.00696 |
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author | Fargnoli, Lucía Panozzo-Zénere, Esteban A. Pagura, Lucas Barisón, María Julia Cricco, Julia A. Silber, Ariel M. Labadie, Guillermo R. |
author_facet | Fargnoli, Lucía Panozzo-Zénere, Esteban A. Pagura, Lucas Barisón, María Julia Cricco, Julia A. Silber, Ariel M. Labadie, Guillermo R. |
author_sort | Fargnoli, Lucía |
collection | PubMed |
description | L-Proline is an important amino acid for the pathogenic protists belonging to Trypanosoma and Leishmania genera. In Trypanosoma cruzi, the etiological agent of Chagas disease, this amino acid is involved in fundamental biological processes such as ATP production, differentiation of the insect and intracellular stages, the host cell infection and the resistance to a variety of stresses. In this study, we explore the L-Proline uptake as a chemotherapeutic target for T. cruzi. Novel inhibitors have been proposed containing the amino acid with a linker and a variable region able to block the transporter. A series of sixteen 1,2,3-triazolyl-proline derivatives have been prepared for in vitro screening against T. cruzi epimastigotes and proline uptake assays. We successfully obtained inhibitors that interfere with the amino acid internalization, which validated our design targeting the metabolite's transport. The presented structures are one of few examples of amino acid transporter inhibitors. The unprecedent application of this strategy on the development of new chemotherapy against Chagas disease, opens a new horizon on antiparasitic drug development against parasitic diseases and other pathologies. |
format | Online Article Text |
id | pubmed-7477874 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74778742020-11-12 Targeting L-Proline Uptake as New Strategy for Anti-chagas Drug Development Fargnoli, Lucía Panozzo-Zénere, Esteban A. Pagura, Lucas Barisón, María Julia Cricco, Julia A. Silber, Ariel M. Labadie, Guillermo R. Front Chem Chemistry L-Proline is an important amino acid for the pathogenic protists belonging to Trypanosoma and Leishmania genera. In Trypanosoma cruzi, the etiological agent of Chagas disease, this amino acid is involved in fundamental biological processes such as ATP production, differentiation of the insect and intracellular stages, the host cell infection and the resistance to a variety of stresses. In this study, we explore the L-Proline uptake as a chemotherapeutic target for T. cruzi. Novel inhibitors have been proposed containing the amino acid with a linker and a variable region able to block the transporter. A series of sixteen 1,2,3-triazolyl-proline derivatives have been prepared for in vitro screening against T. cruzi epimastigotes and proline uptake assays. We successfully obtained inhibitors that interfere with the amino acid internalization, which validated our design targeting the metabolite's transport. The presented structures are one of few examples of amino acid transporter inhibitors. The unprecedent application of this strategy on the development of new chemotherapy against Chagas disease, opens a new horizon on antiparasitic drug development against parasitic diseases and other pathologies. Frontiers Media S.A. 2020-08-25 /pmc/articles/PMC7477874/ /pubmed/33195007 http://dx.doi.org/10.3389/fchem.2020.00696 Text en Copyright © 2020 Fargnoli, Panozzo-Zénere, Pagura, Barisón, Cricco, Silber and Labadie. 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 Fargnoli, Lucía Panozzo-Zénere, Esteban A. Pagura, Lucas Barisón, María Julia Cricco, Julia A. Silber, Ariel M. Labadie, Guillermo R. Targeting L-Proline Uptake as New Strategy for Anti-chagas Drug Development |
title | Targeting L-Proline Uptake as New Strategy for Anti-chagas Drug Development |
title_full | Targeting L-Proline Uptake as New Strategy for Anti-chagas Drug Development |
title_fullStr | Targeting L-Proline Uptake as New Strategy for Anti-chagas Drug Development |
title_full_unstemmed | Targeting L-Proline Uptake as New Strategy for Anti-chagas Drug Development |
title_short | Targeting L-Proline Uptake as New Strategy for Anti-chagas Drug Development |
title_sort | targeting l-proline uptake as new strategy for anti-chagas drug development |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7477874/ https://www.ncbi.nlm.nih.gov/pubmed/33195007 http://dx.doi.org/10.3389/fchem.2020.00696 |
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