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Protease Inhibition—An Established Strategy to Combat Infectious Diseases

Therapeutic agents with novel mechanisms of action are urgently needed to counter the emergence of drug-resistant infections. Several decades of research into proteases of disease agents have revealed enzymes well suited for target-based drug development. Among them are the three recently validated...

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Detalles Bibliográficos
Autores principales: Sojka, Daniel, Šnebergerová, Pavla, Robbertse, Luïse
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197795/
https://www.ncbi.nlm.nih.gov/pubmed/34071206
http://dx.doi.org/10.3390/ijms22115762
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author Sojka, Daniel
Šnebergerová, Pavla
Robbertse, Luïse
author_facet Sojka, Daniel
Šnebergerová, Pavla
Robbertse, Luïse
author_sort Sojka, Daniel
collection PubMed
description Therapeutic agents with novel mechanisms of action are urgently needed to counter the emergence of drug-resistant infections. Several decades of research into proteases of disease agents have revealed enzymes well suited for target-based drug development. Among them are the three recently validated proteolytic targets: proteasomes of the malarial parasite Plasmodium falciparum, aspartyl proteases of P. falciparum (plasmepsins) and the Sars-CoV-2 viral proteases. Despite some unfulfilled expectations over previous decades, the three reviewed targets clearly demonstrate that selective protease inhibitors provide effective therapeutic solutions for the two most impacting infectious diseases nowadays—malaria and COVID-19.
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spelling pubmed-81977952021-06-14 Protease Inhibition—An Established Strategy to Combat Infectious Diseases Sojka, Daniel Šnebergerová, Pavla Robbertse, Luïse Int J Mol Sci Review Therapeutic agents with novel mechanisms of action are urgently needed to counter the emergence of drug-resistant infections. Several decades of research into proteases of disease agents have revealed enzymes well suited for target-based drug development. Among them are the three recently validated proteolytic targets: proteasomes of the malarial parasite Plasmodium falciparum, aspartyl proteases of P. falciparum (plasmepsins) and the Sars-CoV-2 viral proteases. Despite some unfulfilled expectations over previous decades, the three reviewed targets clearly demonstrate that selective protease inhibitors provide effective therapeutic solutions for the two most impacting infectious diseases nowadays—malaria and COVID-19. MDPI 2021-05-28 /pmc/articles/PMC8197795/ /pubmed/34071206 http://dx.doi.org/10.3390/ijms22115762 Text en © 2021 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 Review
Sojka, Daniel
Šnebergerová, Pavla
Robbertse, Luïse
Protease Inhibition—An Established Strategy to Combat Infectious Diseases
title Protease Inhibition—An Established Strategy to Combat Infectious Diseases
title_full Protease Inhibition—An Established Strategy to Combat Infectious Diseases
title_fullStr Protease Inhibition—An Established Strategy to Combat Infectious Diseases
title_full_unstemmed Protease Inhibition—An Established Strategy to Combat Infectious Diseases
title_short Protease Inhibition—An Established Strategy to Combat Infectious Diseases
title_sort protease inhibition—an established strategy to combat infectious diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8197795/
https://www.ncbi.nlm.nih.gov/pubmed/34071206
http://dx.doi.org/10.3390/ijms22115762
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