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On the Reversible and Irreversible Inhibition of Rhodesain by Curcumin

Previously, it was suggested that the natural compound curcumin is an irreversible inhibitor of rhodesain, the major lysosomal cysteine protease of the protozoan parasite Trypanosoma brucei. The suggestion was based on a time-dependent inhibition of the enzyme by curcumin and a lack of recovery of a...

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Detalles Bibliográficos
Autor principal: Steverding, Dietmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983121/
https://www.ncbi.nlm.nih.gov/pubmed/31905815
http://dx.doi.org/10.3390/molecules25010143
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author Steverding, Dietmar
author_facet Steverding, Dietmar
author_sort Steverding, Dietmar
collection PubMed
description Previously, it was suggested that the natural compound curcumin is an irreversible inhibitor of rhodesain, the major lysosomal cysteine protease of the protozoan parasite Trypanosoma brucei. The suggestion was based on a time-dependent inhibition of the enzyme by curcumin and a lack of recovery of activity of the enzyme after pre-incubation with curcumin. This study provides clear evidence that curcumin is a reversible, non-competitive inhibitor of rhodesain. In addition, the study also shows that the apparent irreversible inhibition of curcumin is only observed when no thiol-reducing reagent is included in the measuring buffer and insufficient solubilising agent is added to fully dissolve curcumin in the aqueous solution. Thus, the previous observation that curcumin acts as an irreversible inhibitor for rhodesain was based on a misinterpretation of experimental findings.
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spelling pubmed-69831212020-02-06 On the Reversible and Irreversible Inhibition of Rhodesain by Curcumin Steverding, Dietmar Molecules Article Previously, it was suggested that the natural compound curcumin is an irreversible inhibitor of rhodesain, the major lysosomal cysteine protease of the protozoan parasite Trypanosoma brucei. The suggestion was based on a time-dependent inhibition of the enzyme by curcumin and a lack of recovery of activity of the enzyme after pre-incubation with curcumin. This study provides clear evidence that curcumin is a reversible, non-competitive inhibitor of rhodesain. In addition, the study also shows that the apparent irreversible inhibition of curcumin is only observed when no thiol-reducing reagent is included in the measuring buffer and insufficient solubilising agent is added to fully dissolve curcumin in the aqueous solution. Thus, the previous observation that curcumin acts as an irreversible inhibitor for rhodesain was based on a misinterpretation of experimental findings. MDPI 2019-12-30 /pmc/articles/PMC6983121/ /pubmed/31905815 http://dx.doi.org/10.3390/molecules25010143 Text en © 2019 by the author. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Steverding, Dietmar
On the Reversible and Irreversible Inhibition of Rhodesain by Curcumin
title On the Reversible and Irreversible Inhibition of Rhodesain by Curcumin
title_full On the Reversible and Irreversible Inhibition of Rhodesain by Curcumin
title_fullStr On the Reversible and Irreversible Inhibition of Rhodesain by Curcumin
title_full_unstemmed On the Reversible and Irreversible Inhibition of Rhodesain by Curcumin
title_short On the Reversible and Irreversible Inhibition of Rhodesain by Curcumin
title_sort on the reversible and irreversible inhibition of rhodesain by curcumin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6983121/
https://www.ncbi.nlm.nih.gov/pubmed/31905815
http://dx.doi.org/10.3390/molecules25010143
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