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...
- 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/
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Repositorio UdeA |
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|
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 |
dc.type.hasversion.spa.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.coar.spa.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
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 |
dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by/2.5/co/ |
dc.rights.accessrights.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.creativecommons.spa.fl_str_mv |
https://creativecommons.org/licenses/by/4.0/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/2.5/co/ http://purl.org/coar/access_right/c_abf2 https://creativecommons.org/licenses/by/4.0/ |
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 http://bibliotecadigital.udea.edu.co/bitstream/10495/23809/3/license.txt http://bibliotecadigital.udea.edu.co/bitstream/10495/23809/2/license_rdf |
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Repositorio Institucional Universidad de Antioquia |
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andres.perez@udea.edu.co |
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1812173121245937664 |
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.coTk9URTogUExBQ0UgWU9VUiBPV04gTElDRU5TRSBIRVJFClRoaXMgc2FtcGxlIGxpY2Vuc2UgaXMgcHJvdmlkZWQgZm9yIGluZm9ybWF0aW9uYWwgcHVycG9zZXMgb25seS4KCk5PTi1FWENMVVNJVkUgRElTVFJJQlVUSU9OIExJQ0VOU0UKCkJ5IHNpZ25pbmcgYW5kIHN1Ym1pdHRpbmcgdGhpcyBsaWNlbnNlLCB5b3UgKHRoZSBhdXRob3Iocykgb3IgY29weXJpZ2h0Cm93bmVyKSBncmFudHMgdG8gRFNwYWNlIFVuaXZlcnNpdHkgKERTVSkgdGhlIG5vbi1leGNsdXNpdmUgcmlnaHQgdG8gcmVwcm9kdWNlLAp0cmFuc2xhdGUgKGFzIGRlZmluZWQgYmVsb3cpLCBhbmQvb3IgZGlzdHJpYnV0ZSB5b3VyIHN1Ym1pc3Npb24gKGluY2x1ZGluZwp0aGUgYWJzdHJhY3QpIHdvcmxkd2lkZSBpbiBwcmludCBhbmQgZWxlY3Ryb25pYyBmb3JtYXQgYW5kIGluIGFueSBtZWRpdW0sCmluY2x1ZGluZyBidXQgbm90IGxpbWl0ZWQgdG8gYXVkaW8gb3IgdmlkZW8uCgpZb3UgYWdyZWUgdGhhdCBEU1UgbWF5LCB3aXRob3V0IGNoYW5naW5nIHRoZSBjb250ZW50LCB0cmFuc2xhdGUgdGhlCnN1Ym1pc3Npb24gdG8gYW55IG1lZGl1bSBvciBmb3JtYXQgZm9yIHRoZSBwdXJwb3NlIG9mIHByZXNlcnZhdGlvbi4KCllvdSBhbHNvIGFncmVlIHRoYXQgRFNVIG1heSBrZWVwIG1vcmUgdGhhbiBvbmUgY29weSBvZiB0aGlzIHN1Ym1pc3Npb24gZm9yCnB1cnBvc2VzIG9mIHNlY3VyaXR5LCBiYWNrLXVwIGFuZCBwcmVzZXJ2YXRpb24uCgpZb3UgcmVwcmVzZW50IHRoYXQgdGhlIHN1Ym1pc3Npb24gaXMgeW91ciBvcmlnaW5hbCB3b3JrLCBhbmQgdGhhdCB5b3UgaGF2ZQp0aGUgcmlnaHQgdG8gZ3JhbnQgdGhlIHJpZ2h0cyBjb250YWluZWQgaW4gdGhpcyBsaWNlbnNlLiBZb3UgYWxzbyByZXByZXNlbnQKdGhhdCB5b3VyIHN1Ym1pc3Npb24gZG9lcyBub3QsIHRvIHRoZSBiZXN0IG9mIHlvdXIga25vd2xlZGdlLCBpbmZyaW5nZSB1cG9uCmFueW9uZSdzIGNvcHlyaWdodC4KCklmIHRoZSBzdWJtaXNzaW9uIGNvbnRhaW5zIG1hdGVyaWFsIGZvciB3aGljaCB5b3UgZG8gbm90IGhvbGQgY29weXJpZ2h0LAp5b3UgcmVwcmVzZW50IHRoYXQgeW91IGhhdmUgb2J0YWluZWQgdGhlIHVucmVzdHJpY3RlZCBwZXJtaXNzaW9uIG9mIHRoZQpjb3B5cmlnaHQgb3duZXIgdG8gZ3JhbnQgRFNVIHRoZSByaWdodHMgcmVxdWlyZWQgYnkgdGhpcyBsaWNlbnNlLCBhbmQgdGhhdApzdWNoIHRoaXJkLXBhcnR5IG93bmVkIG1hdGVyaWFsIGlzIGNsZWFybHkgaWRlbnRpZmllZCBhbmQgYWNrbm93bGVkZ2VkCndpdGhpbiB0aGUgdGV4dCBvciBjb250ZW50IG9mIHRoZSBzdWJtaXNzaW9uLgoKSUYgVEhFIFNVQk1JU1NJT04gSVMgQkFTRUQgVVBPTiBXT1JLIFRIQVQgSEFTIEJFRU4gU1BPTlNPUkVEIE9SIFNVUFBPUlRFRApCWSBBTiBBR0VOQ1kgT1IgT1JHQU5JWkFUSU9OIE9USEVSIFRIQU4gRFNVLCBZT1UgUkVQUkVTRU5UIFRIQVQgWU9VIEhBVkUKRlVMRklMTEVEIEFOWSBSSUdIVCBPRiBSRVZJRVcgT1IgT1RIRVIgT0JMSUdBVElPTlMgUkVRVUlSRUQgQlkgU1VDSApDT05UUkFDVCBPUiBBR1JFRU1FTlQuCgpEU1Ugd2lsbCBjbGVhcmx5IGlkZW50aWZ5IHlvdXIgbmFtZShzKSBhcyB0aGUgYXV0aG9yKHMpIG9yIG93bmVyKHMpIG9mIHRoZQpzdWJtaXNzaW9uLCBhbmQgd2lsbCBub3QgbWFrZSBhbnkgYWx0ZXJhdGlvbiwgb3RoZXIgdGhhbiBhcyBhbGxvd2VkIGJ5IHRoaXMKbGljZW5zZSwgdG8geW91ciBzdWJtaXNzaW9uLgo= |