Molecular interaction assays in silico of crotapotin from Crotalus durissus terrificus against the molecular target trypanothione reductase from Leishmania braziliensis

Abstract Background: Leishmaniasis is a neglected disease that mainly affects impoverished populations and receives limited attention from governments and research institutions. Current treatments are based on antimonial therapies, which present high toxicity and cause significant side effects, su...

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Main Authors: Jamile Mariano Macedo, Mateus Farias Souza, Anderson Maciel Lima, Aleff Ferreira Francisco, Anderson Makoto Kayano, Maria Elisabeth Moreira de Lima Gusmão, Erika Crhistina Santos de Araújo, Guilherme Henrique Marchi Salvador, Marcos Roberto de Mattos Fontes, Juliana Pavan Zuliani, Andreimar Martins Soares
Format: Article
Language:English
Published: SciELO 2025-04-01
Series:Journal of Venomous Animals and Toxins including Tropical Diseases
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Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992025000100306&lng=en&tlng=en
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author Jamile Mariano Macedo
Mateus Farias Souza
Anderson Maciel Lima
Aleff Ferreira Francisco
Anderson Makoto Kayano
Maria Elisabeth Moreira de Lima Gusmão
Erika Crhistina Santos de Araújo
Guilherme Henrique Marchi Salvador
Marcos Roberto de Mattos Fontes
Juliana Pavan Zuliani
Andreimar Martins Soares
author_facet Jamile Mariano Macedo
Mateus Farias Souza
Anderson Maciel Lima
Aleff Ferreira Francisco
Anderson Makoto Kayano
Maria Elisabeth Moreira de Lima Gusmão
Erika Crhistina Santos de Araújo
Guilherme Henrique Marchi Salvador
Marcos Roberto de Mattos Fontes
Juliana Pavan Zuliani
Andreimar Martins Soares
author_sort Jamile Mariano Macedo
collection DOAJ
description Abstract Background: Leishmaniasis is a neglected disease that mainly affects impoverished populations and receives limited attention from governments and research institutions. Current treatments are based on antimonial therapies, which present high toxicity and cause significant side effects, such as cardiotoxicity and hepatotoxicity. This study proposes using crotapotin, isolated from Crotalus durissus terrificus venom, as a potential inhibitor of the enzyme trypanothione reductase from Leishmania braziliensis (LbTR). Methods: In silico assays were conducted to evaluate the interaction of crotapotin with LbTR using molecular docking and molecular dynamics techniques. Recombinant LbTR was expressed in E. coli, and its enzymatic activity was confirmed. The inhibitory action of crotapotin on LbTR was then tested in enzymatic assays. Results: The stability of these interactions was confirmed over 200 ns molecular dynamics simulations, with a clustering analysis using the GROMACS method revealing a total of 12 distinct clusters. The five most representative clusters showed low RMSD values, indicating high structural stability of the LbTR-crotapotin complex. In particular, cluster 1, with 3,398 frames and an average RMSD of 0.189 nm from the centroid, suggests a dominant stable conformation of the complex. Additional clusters maintained average RMSD values between 0.173 nm and 0.193 nm, further reinforcing the robustness of the complex under physiological conditions. Recombinant LbTR expression was successful, yielding 4.8 mg/L with high purity, as verified by SDS-PAGE. In the enzymatic assays, crotapotin partially inhibited LbTR activity, with an IC50 of 223.4 μM. Conclusion: The in silico findings suggest a stable and structured interaction between crotapotin and LbTR, with low structural fluctuation, although the inhibition observed in in vitro assays was moderate. These results indicate the potential of crotapotin as a promising basis for developing specific LbTR inhibitors, contributing to the bioprospecting of new antiparasitic agents.
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spelling doaj-art-79a7efcc5bb7499a86aeee85ef8afec22025-08-20T02:08:40ZengSciELOJournal of Venomous Animals and Toxins including Tropical Diseases1678-91992025-04-013110.1590/1678-9199-jvatitd-2024-0049Molecular interaction assays in silico of crotapotin from Crotalus durissus terrificus against the molecular target trypanothione reductase from Leishmania braziliensisJamile Mariano Macedohttps://orcid.org/0000-0002-9420-6282Mateus Farias Souzahttps://orcid.org/0000-0001-5834-3389Anderson Maciel Limahttps://orcid.org/0000-0001-9755-7929Aleff Ferreira Franciscohttps://orcid.org/0000-0002-6492-5729Anderson Makoto Kayanohttps://orcid.org/0000-0003-4418-7850Maria Elisabeth Moreira de Lima Gusmãohttps://orcid.org/0009-0003-8235-6181Erika Crhistina Santos de Araújohttps://orcid.org/0000-0002-1928-9196Guilherme Henrique Marchi Salvadorhttps://orcid.org/0000-0001-7459-7637Marcos Roberto de Mattos Fonteshttps://orcid.org/0000-0002-4634-6221Juliana Pavan Zulianihttps://orcid.org/0000-0001-9221-7749Andreimar Martins Soareshttps://orcid.org/0000-0003-1032-2188Abstract Background: Leishmaniasis is a neglected disease that mainly affects impoverished populations and receives limited attention from governments and research institutions. Current treatments are based on antimonial therapies, which present high toxicity and cause significant side effects, such as cardiotoxicity and hepatotoxicity. This study proposes using crotapotin, isolated from Crotalus durissus terrificus venom, as a potential inhibitor of the enzyme trypanothione reductase from Leishmania braziliensis (LbTR). Methods: In silico assays were conducted to evaluate the interaction of crotapotin with LbTR using molecular docking and molecular dynamics techniques. Recombinant LbTR was expressed in E. coli, and its enzymatic activity was confirmed. The inhibitory action of crotapotin on LbTR was then tested in enzymatic assays. Results: The stability of these interactions was confirmed over 200 ns molecular dynamics simulations, with a clustering analysis using the GROMACS method revealing a total of 12 distinct clusters. The five most representative clusters showed low RMSD values, indicating high structural stability of the LbTR-crotapotin complex. In particular, cluster 1, with 3,398 frames and an average RMSD of 0.189 nm from the centroid, suggests a dominant stable conformation of the complex. Additional clusters maintained average RMSD values between 0.173 nm and 0.193 nm, further reinforcing the robustness of the complex under physiological conditions. Recombinant LbTR expression was successful, yielding 4.8 mg/L with high purity, as verified by SDS-PAGE. In the enzymatic assays, crotapotin partially inhibited LbTR activity, with an IC50 of 223.4 μM. Conclusion: The in silico findings suggest a stable and structured interaction between crotapotin and LbTR, with low structural fluctuation, although the inhibition observed in in vitro assays was moderate. These results indicate the potential of crotapotin as a promising basis for developing specific LbTR inhibitors, contributing to the bioprospecting of new antiparasitic agents.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992025000100306&lng=en&tlng=enSnake venomsInhibitionNeglected tropical diseasesMolecular dynamicsRecombinant expression
spellingShingle Jamile Mariano Macedo
Mateus Farias Souza
Anderson Maciel Lima
Aleff Ferreira Francisco
Anderson Makoto Kayano
Maria Elisabeth Moreira de Lima Gusmão
Erika Crhistina Santos de Araújo
Guilherme Henrique Marchi Salvador
Marcos Roberto de Mattos Fontes
Juliana Pavan Zuliani
Andreimar Martins Soares
Molecular interaction assays in silico of crotapotin from Crotalus durissus terrificus against the molecular target trypanothione reductase from Leishmania braziliensis
Journal of Venomous Animals and Toxins including Tropical Diseases
Snake venoms
Inhibition
Neglected tropical diseases
Molecular dynamics
Recombinant expression
title Molecular interaction assays in silico of crotapotin from Crotalus durissus terrificus against the molecular target trypanothione reductase from Leishmania braziliensis
title_full Molecular interaction assays in silico of crotapotin from Crotalus durissus terrificus against the molecular target trypanothione reductase from Leishmania braziliensis
title_fullStr Molecular interaction assays in silico of crotapotin from Crotalus durissus terrificus against the molecular target trypanothione reductase from Leishmania braziliensis
title_full_unstemmed Molecular interaction assays in silico of crotapotin from Crotalus durissus terrificus against the molecular target trypanothione reductase from Leishmania braziliensis
title_short Molecular interaction assays in silico of crotapotin from Crotalus durissus terrificus against the molecular target trypanothione reductase from Leishmania braziliensis
title_sort molecular interaction assays in silico of crotapotin from crotalus durissus terrificus against the molecular target trypanothione reductase from leishmania braziliensis
topic Snake venoms
Inhibition
Neglected tropical diseases
Molecular dynamics
Recombinant expression
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1678-91992025000100306&lng=en&tlng=en
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