Novel neuroprotective peptides in the venom of the solitary scoliid wasp Scolia decorata ventralis

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dc.contributorLab. Imunoquímicapt_BR
dc.contributor.authorAlberto-Silva, Carlospt_BR
dc.contributor.authorPortaro, Fernanda Calheta Vieirapt_BR
dc.contributor.authorKodama, Roberto Tadashipt_BR
dc.contributor.authorPantaleão, Halyne Queirozpt_BR
dc.contributor.authorRangel, Marisapt_BR
dc.contributor.authorNihei, Ken-ichipt_BR
dc.contributor.authorKonno, Katsuhiropt_BR
dc.date.accessioned2021-07-08T18:39:15Z-
dc.date.available2021-07-08T18:39:15Z-
dc.date.issued2021pt_BR
dc.identifier.citationAlberto-Silva C, Portaro FCV, Kodama RT, Pantaleão HQ, Rangel M, Nihei K-, et al. Novel neuroprotective peptides in the venom of the solitary scoliid wasp Scolia decorata ventralis. J. Venom. Anim. Toxins Incl. Trop. Dis.. 2021 June;27:e20200171pt_BR
dc.identifier.urihttps://repositorio.butantan.gov.br/handle/butantan/3883-
dc.description.abstractBackground Solitary wasp venoms may be a rich source of neuroactive substances, since their venoms are used for paralyzing preys. We have been exploring bioactive constituents of solitary wasp venoms and, in this study, the component profile of the venom from a solitary scoliid wasp, Scolia decorata ventralis, was investigated through a comprehensive analysis using LC-MS. Two peptides were synthesized, and their neuroprotective properties were evaluated. Methods A reverse-phase HPLC connected to ESI-MS was used for LC-MS analyses. Online mass fingerprinting was performed from TIC, and data-dependent tandem mass spectrometry gave the MS/MS spectra. The sequences of two major peptide components were determined by MALDI-TOF/TOF MS analysis, confirmed by solid phase synthesis. Using the synthetic peptides, biological activities were assessed. Cell integrity tests and neuroprotection analyzes using H2O2 as an oxidative stress inducer were performed for both peptides. Results Online mass fingerprinting revealed that the venom contains 123 components, and the MS/MS analysis resulted in 33 full sequences of peptide components. The two main peptides, α-scoliidine (DYVTVKGFSPLR) and β-scoliidine (DYVTVKGFSPLRKA), present homology with the bradykinin C-terminal. Despite this, both peptides did not behave as substrates or inhibitors of ACE, indicating that they do not interact with this metallopeptidase. In further studies, β-scoliidine, but not α -scoliidine, showed protective effects against oxidative stress-induced neurotoxicity in PC12 cells through integrity and metabolism cell assays. Interestingly, β-scoliidine has the extension of the KA dipeptide at the C-terminal in comparison with α-scoliidine. Conclusion Comprehensive LC-MS and MS/MS analyses from the Scolia decorata ventralis venom displayed the component profile of this venom. β-scoliidine showed an effective cytoprotective effect, probably due to the observed increase in the number of cells. This is the first report of solitary wasp venom peptides showing neuroprotective activity.pt_BR
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)pt_BR
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)pt_BR
dc.format.extente20200171pt_BR
dc.language.isoEnglishpt_BR
dc.relation.ispartofJournal of Venomous Animals and Toxins Including Tropical Diseasespt_BR
dc.rightsOpen accesspt_BR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/pt_BR
dc.titleNovel neuroprotective peptides in the venom of the solitary scoliid wasp Scolia decorata ventralispt_BR
dc.typeArticlept_BR
dc.rights.licenseCC BYpt_BR
dc.identifier.doi10.1590/1678-9199-JVATITD-2020-0171pt_BR
dc.identifier.urlhttps://doi.org/10.1590/1678-9199-JVATITD-2020-0171pt_BR
dc.contributor.externalUniversidade Federal do ABC (UFABC)pt_BR
dc.contributor.externalUtsunomiya Universitypt_BR
dc.contributor.externalUniversity of Toyamapt_BR
dc.identifier.citationvolume27pt_BR
dc.subject.keywordComprehensive analysispt_BR
dc.subject.keywordLC-ESI-MSpt_BR
dc.subject.keywordSolitary wasppt_BR
dc.subject.keywordVenompt_BR
dc.subject.keywordNeuroprotective peptidept_BR
dc.relation.ispartofabbreviatedJ. Venom. Anim. Toxins Incl. Trop. Dis.pt_BR
dc.identifier.citationabntv. 27, e20200171, jun. 2021pt_BR
dc.identifier.citationvancouver2021 June;27:e20200171pt_BR
dc.contributor.butantanPortaro, Fernanda Calheta Vieira|:Pesquisador:Docente permanente PPGTOX|:Lab. Imunoquímicapt_BR
dc.contributor.butantanKodama, Roberto Tadashi|:Aluno|:Lab. Imunoquímicapt_BR
dc.contributor.butantanRangel, Marisa|:Pesquisador|:Lab. Imunoquímicapt_BR
dc.sponsorship.butantanFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)¦¦pt_BR
dc.sponsorship.butantanCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)¦¦001pt_BR
dc.identifier.bvsccBR78.1pt_BR
dc.identifier.bvsdbIBProdpt_BR
dc.description.dbindexedYespt_BR
item.languageiso639-1English-
item.fulltextCom Texto completo-
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