The synthetic varespladib molecule is a multi-functional inhibitor for PLA2 and PLA2-like ophidic toxins
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , |
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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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:29462024-08-05T15:04:45.882716Repositório 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) |
repository.mail.fl_str_mv |
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1808128456091762688 |