Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experiments

ABSTRACT: Small molecule inhibitors of snake venom metalloproteinases (SVMPs) could provide a means to rapidly halt the progression of local tissue damage following viperid snake envenomations. In this study, we examine the ability of candidate compounds based on a pentacyclic triterpene skeleton to...

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Autores:
Preciado Rojo, Lina María
Pereañez Jiménez, Jaime Andrés
Azhagiya Singam, Ettayapuram Ramaprasad
Comer, Jeffrey
Tipo de recurso:
Article of investigation
Fecha de publicación:
2018
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/23809
Acceso en línea:
http://hdl.handle.net/10495/23809
Palabra clave:
Venenos de Serpiente
Snake Venoms
Simulación de Dinámica Molecular
Molecular Dynamics Simulation
Triterpenos
Triterpenes
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
id UDEA2_0079f4a90f68fc2ee62a37a7e97e9501
oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/23809
network_acronym_str UDEA2
network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experiments
title Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experiments
spellingShingle Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experiments
Venenos de Serpiente
Snake Venoms
Simulación de Dinámica Molecular
Molecular Dynamics Simulation
Triterpenos
Triterpenes
title_short Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experiments
title_full Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experiments
title_fullStr Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experiments
title_full_unstemmed Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experiments
title_sort Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experiments
dc.creator.fl_str_mv Preciado Rojo, Lina María
Pereañez Jiménez, Jaime Andrés
Azhagiya Singam, Ettayapuram Ramaprasad
Comer, Jeffrey
dc.contributor.author.none.fl_str_mv Preciado Rojo, Lina María
Pereañez Jiménez, Jaime Andrés
Azhagiya Singam, Ettayapuram Ramaprasad
Comer, Jeffrey
dc.subject.decs.none.fl_str_mv Venenos de Serpiente
Snake Venoms
Simulación de Dinámica Molecular
Molecular Dynamics Simulation
Triterpenos
Triterpenes
topic Venenos de Serpiente
Snake Venoms
Simulación de Dinámica Molecular
Molecular Dynamics Simulation
Triterpenos
Triterpenes
description ABSTRACT: Small molecule inhibitors of snake venom metalloproteinases (SVMPs) could provide a means to rapidly halt the progression of local tissue damage following viperid snake envenomations. In this study, we examine the ability of candidate compounds based on a pentacyclic triterpene skeleton to inhibit SVMPs. We leverage molecular dynamics simulations to estimate the free energies of the candidate compounds for binding to BaP1, a P-I type SVMP, and compare these results with experimental assays of proteolytic activity inhibition in a homologous enzyme (Batx-I). Both simulation and experiment suggest that betulinic acid is the most active candidate, with the simulations predicting a standard binding free energy of DG = 11.0 1.4 kcal/mol. The simulations also reveal the atomic interactions that underlie binding between the triterpenic acids and BaP1, most notably the electrostatic interaction between carboxylate groups of the compounds and the zinc cofactor of BaP1. Together, our simulations and experiments suggest that occlusion of the S10 subsite is essential for inhibition of proteolytic activity. While all active compounds make hydrophobic contacts in the S10 site, b-boswellic acid, with its distinct carboxylate position, does not occlude the S10 site in simulation and exhibits negligible activity in experiment.
publishDate 2018
dc.date.issued.none.fl_str_mv 2018
dc.date.accessioned.none.fl_str_mv 2021-11-05T23:34:49Z
dc.date.available.none.fl_str_mv 2021-11-05T23:34:49Z
dc.type.spa.fl_str_mv info:eu-repo/semantics/article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
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dc.type.redcol.spa.fl_str_mv https://purl.org/redcol/resource_type/ART
dc.type.local.spa.fl_str_mv Artículo de investigación
format http://purl.org/coar/resource_type/c_2df8fbb1
status_str publishedVersion
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10495/23809
dc.identifier.doi.none.fl_str_mv 10.3390/toxins10100397
dc.identifier.eissn.none.fl_str_mv 2072-6651
url http://hdl.handle.net/10495/23809
identifier_str_mv 10.3390/toxins10100397
2072-6651
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Toxins
dc.rights.spa.fl_str_mv info:eu-repo/semantics/openAccess
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dc.rights.accessrights.spa.fl_str_mv http://purl.org/coar/access_right/c_abf2
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dc.format.extent.spa.fl_str_mv 20
dc.format.mimetype.spa.fl_str_mv application/pdf
dc.publisher.spa.fl_str_mv MDPI
dc.publisher.group.spa.fl_str_mv Toxinología Alternativas Terapéuticas y Alimentarias
dc.publisher.place.spa.fl_str_mv Basilea, Suiza
institution Universidad de Antioquia
bitstream.url.fl_str_mv http://bibliotecadigital.udea.edu.co/bitstream/10495/23809/1/PreciadoLina_2018_InteractionsBetweenTriterpenesTypeSnake.pdf
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spelling Preciado Rojo, Lina MaríaPereañez Jiménez, Jaime AndrésAzhagiya Singam, Ettayapuram RamaprasadComer, Jeffrey2021-11-05T23:34:49Z2021-11-05T23:34:49Z2018http://hdl.handle.net/10495/2380910.3390/toxins101003972072-6651ABSTRACT: Small molecule inhibitors of snake venom metalloproteinases (SVMPs) could provide a means to rapidly halt the progression of local tissue damage following viperid snake envenomations. In this study, we examine the ability of candidate compounds based on a pentacyclic triterpene skeleton to inhibit SVMPs. We leverage molecular dynamics simulations to estimate the free energies of the candidate compounds for binding to BaP1, a P-I type SVMP, and compare these results with experimental assays of proteolytic activity inhibition in a homologous enzyme (Batx-I). Both simulation and experiment suggest that betulinic acid is the most active candidate, with the simulations predicting a standard binding free energy of DG = 11.0 1.4 kcal/mol. The simulations also reveal the atomic interactions that underlie binding between the triterpenic acids and BaP1, most notably the electrostatic interaction between carboxylate groups of the compounds and the zinc cofactor of BaP1. Together, our simulations and experiments suggest that occlusion of the S10 subsite is essential for inhibition of proteolytic activity. While all active compounds make hydrophobic contacts in the S10 site, b-boswellic acid, with its distinct carboxylate position, does not occlude the S10 site in simulation and exhibits negligible activity in experiment.COL001447620application/pdfengMDPIToxinología Alternativas Terapéuticas y AlimentariasBasilea, Suizainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARTArtículo de investigaciónhttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/2.5/co/http://purl.org/coar/access_right/c_abf2https://creativecommons.org/licenses/by/4.0/Interactions between triterpenes and a P-I type snake venom metalloproteinase: Molecular simulations and experimentsVenenos de SerpienteSnake VenomsSimulación de Dinámica MolecularMolecular Dynamics SimulationTriterpenosTriterpenesToxinsToxins1201010ORIGINALPreciadoLina_2018_InteractionsBetweenTriterpenesTypeSnake.pdfPreciadoLina_2018_InteractionsBetweenTriterpenesTypeSnake.pdfArtículo de investigaciónapplication/pdf6360475http://bibliotecadigital.udea.edu.co/bitstream/10495/23809/1/PreciadoLina_2018_InteractionsBetweenTriterpenesTypeSnake.pdf9ea5d038cab6788e07fd5c2c35b8309dMD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748http://bibliotecadigital.udea.edu.co/bitstream/10495/23809/3/license.txt8a4605be74aa9ea9d79846c1fba20a33MD53CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8927http://bibliotecadigital.udea.edu.co/bitstream/10495/23809/2/license_rdf1646d1f6b96dbbbc38035efc9239ac9cMD5210495/23809oai:bibliotecadigital.udea.edu.co:10495/238092021-11-05 18:34:49.788Repositorio Institucional Universidad de Antioquiaandres.perez@udea.edu.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