The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins

Detalhes bibliográficos
Autor(a) principal: Salvador, Guilherme H.M. [UNESP]
Data de Publicação: 2021
Outros Autores: Borges, Rafael J. [UNESP], Lomonte, Bruno, Lewin, Matthew R., Fontes, Marcos R.M. [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.bbagen.2021.129913
http://hdl.handle.net/11449/206214
Resumo: Background: The treatment for snakebites is early administration of antivenom, which can be highly effective in inhibiting the systemic effects of snake venoms, but is less effective in the treatment of extra-circulatory and local effects. To complement standard-of-care treatments such as antibody-based antivenoms, natural and synthetic small molecules have been proposed for the inhibition of key venom components such as phospholipase A2 (PLA2) and PLA2-like toxins. Varespladib (compound LY315920) is a synthetic molecule developed and clinically tested aiming to block inflammatory cascades of several diseases associated with high PLA2s. Recent studies have demonstrated this molecule is able to potently inhibit snake venom catalytic PLA2 and PLA2-like toxins. Methods: In vivo and in vitro techniques were used to evaluate the inhibitory effect of varespladib against MjTX-I. X-ray crystallography was used to reveal details of the interaction between these molecules. A new methodology that combines crystallography, mass spectroscopy and phylogenetic data was used to review its primary sequence. Results: Varespladib was able to inhibit the myotoxic and cytotoxic effects of MjTX-I. Structural analysis revealed a particular inhibitory mechanism of MjTX-I when compared to other PLA2-like myotoxin, presenting an oligomeric-independent function. Conclusion: Results suggest the effectiveness of varespladib for the inhibition of MjTX-I, in similarity with other PLA2 and PLA2-like toxins. General significance: Varespladib appears to be a promissory molecule in the treatment of local effects led by PLA2 and PLA2-like toxins (oligomeric dependent and independent), indicating that this is a multifunctional or broadly specific inhibitor for different toxins within this superfamily.
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spelling The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxinsLys49-phospholipases A2 proteinsMyotoxicity inhibitionPhospholipase A2 - like proteinsPhospholipase A2 inhibitorSnake venomVarespladib inhibitorBackground: The treatment for snakebites is early administration of antivenom, which can be highly effective in inhibiting the systemic effects of snake venoms, but is less effective in the treatment of extra-circulatory and local effects. To complement standard-of-care treatments such as antibody-based antivenoms, natural and synthetic small molecules have been proposed for the inhibition of key venom components such as phospholipase A2 (PLA2) and PLA2-like toxins. Varespladib (compound LY315920) is a synthetic molecule developed and clinically tested aiming to block inflammatory cascades of several diseases associated with high PLA2s. Recent studies have demonstrated this molecule is able to potently inhibit snake venom catalytic PLA2 and PLA2-like toxins. Methods: In vivo and in vitro techniques were used to evaluate the inhibitory effect of varespladib against MjTX-I. X-ray crystallography was used to reveal details of the interaction between these molecules. A new methodology that combines crystallography, mass spectroscopy and phylogenetic data was used to review its primary sequence. Results: Varespladib was able to inhibit the myotoxic and cytotoxic effects of MjTX-I. Structural analysis revealed a particular inhibitory mechanism of MjTX-I when compared to other PLA2-like myotoxin, presenting an oligomeric-independent function. Conclusion: Results suggest the effectiveness of varespladib for the inhibition of MjTX-I, in similarity with other PLA2 and PLA2-like toxins. General significance: Varespladib appears to be a promissory molecule in the treatment of local effects led by PLA2 and PLA2-like toxins (oligomeric dependent and independent), indicating that this is a multifunctional or broadly specific inhibitor for different toxins within this superfamily.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Departamento de Biofísica e Farmacologia Instituto de Biociências Universidade Estadual Paulista (UNESP)Instituto Clodomiro Picado Facultad de Microbiología Universidad de Costa RicaCenter for Exploration and Travel Health California Academy of SciencesDepartamento de Biofísica e Farmacologia Instituto de Biociências Universidade Estadual Paulista (UNESP)FAPESP: 2015/17286-0FAPESP: 2016/24191-8CNPq: 302883/2017-7Universidade Estadual Paulista (Unesp)Universidad de Costa RicaCalifornia Academy of SciencesSalvador, Guilherme H.M. [UNESP]Borges, Rafael J. [UNESP]Lomonte, BrunoLewin, Matthew R.Fontes, Marcos R.M. [UNESP]2021-06-25T10:28:22Z2021-06-25T10:28:22Z2021-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.bbagen.2021.129913Biochimica et Biophysica Acta - General Subjects, v. 1865, n. 7, 2021.1872-80060304-4165http://hdl.handle.net/11449/20621410.1016/j.bbagen.2021.1299132-s2.0-85104386648Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiochimica et Biophysica Acta - General Subjectsinfo:eu-repo/semantics/openAccess2021-10-22T22:24:12Zoai:repositorio.unesp.br:11449/206214Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-22T22:24:12Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins
title The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins
spellingShingle The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins
Salvador, Guilherme H.M. [UNESP]
Lys49-phospholipases A2 proteins
Myotoxicity inhibition
Phospholipase A2 - like proteins
Phospholipase A2 inhibitor
Snake venom
Varespladib inhibitor
title_short The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins
title_full The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins
title_fullStr The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins
title_full_unstemmed The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins
title_sort The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins
author Salvador, Guilherme H.M. [UNESP]
author_facet Salvador, Guilherme H.M. [UNESP]
Borges, Rafael J. [UNESP]
Lomonte, Bruno
Lewin, Matthew R.
Fontes, Marcos R.M. [UNESP]
author_role author
author2 Borges, Rafael J. [UNESP]
Lomonte, Bruno
Lewin, Matthew R.
Fontes, Marcos R.M. [UNESP]
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
Universidad de Costa Rica
California Academy of Sciences
dc.contributor.author.fl_str_mv Salvador, Guilherme H.M. [UNESP]
Borges, Rafael J. [UNESP]
Lomonte, Bruno
Lewin, Matthew R.
Fontes, Marcos R.M. [UNESP]
dc.subject.por.fl_str_mv Lys49-phospholipases A2 proteins
Myotoxicity inhibition
Phospholipase A2 - like proteins
Phospholipase A2 inhibitor
Snake venom
Varespladib inhibitor
topic Lys49-phospholipases A2 proteins
Myotoxicity inhibition
Phospholipase A2 - like proteins
Phospholipase A2 inhibitor
Snake venom
Varespladib inhibitor
description Background: The treatment for snakebites is early administration of antivenom, which can be highly effective in inhibiting the systemic effects of snake venoms, but is less effective in the treatment of extra-circulatory and local effects. To complement standard-of-care treatments such as antibody-based antivenoms, natural and synthetic small molecules have been proposed for the inhibition of key venom components such as phospholipase A2 (PLA2) and PLA2-like toxins. Varespladib (compound LY315920) is a synthetic molecule developed and clinically tested aiming to block inflammatory cascades of several diseases associated with high PLA2s. Recent studies have demonstrated this molecule is able to potently inhibit snake venom catalytic PLA2 and PLA2-like toxins. Methods: In vivo and in vitro techniques were used to evaluate the inhibitory effect of varespladib against MjTX-I. X-ray crystallography was used to reveal details of the interaction between these molecules. A new methodology that combines crystallography, mass spectroscopy and phylogenetic data was used to review its primary sequence. Results: Varespladib was able to inhibit the myotoxic and cytotoxic effects of MjTX-I. Structural analysis revealed a particular inhibitory mechanism of MjTX-I when compared to other PLA2-like myotoxin, presenting an oligomeric-independent function. Conclusion: Results suggest the effectiveness of varespladib for the inhibition of MjTX-I, in similarity with other PLA2 and PLA2-like toxins. General significance: Varespladib appears to be a promissory molecule in the treatment of local effects led by PLA2 and PLA2-like toxins (oligomeric dependent and independent), indicating that this is a multifunctional or broadly specific inhibitor for different toxins within this superfamily.
publishDate 2021
dc.date.none.fl_str_mv 2021-06-25T10:28:22Z
2021-06-25T10:28:22Z
2021-07-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.bbagen.2021.129913
Biochimica et Biophysica Acta - General Subjects, v. 1865, n. 7, 2021.
1872-8006
0304-4165
http://hdl.handle.net/11449/206214
10.1016/j.bbagen.2021.129913
2-s2.0-85104386648
url http://dx.doi.org/10.1016/j.bbagen.2021.129913
http://hdl.handle.net/11449/206214
identifier_str_mv Biochimica et Biophysica Acta - General Subjects, v. 1865, n. 7, 2021.
1872-8006
0304-4165
10.1016/j.bbagen.2021.129913
2-s2.0-85104386648
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biochimica et Biophysica Acta - General Subjects
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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