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Mapping possible interaction sites for crotoxin in CNF, a gamma PLA2 inhibitor from Crotalus durissus terrificus rattle snake, using SPOT synthesis

dc.contributor.authorCampos, Patricia Cota
dc.contributor.authorOliveira, Hamine Cristina de [UNESP]
dc.contributor.authorOrtolani, Paula Ladeira
dc.contributor.authorAmaral de Melo, Lutiana
dc.contributor.authorFontes, Marcos R.M. [UNESP]
dc.contributor.authorFortes-Dias, Consuelo Latorre
dc.contributor.institutionFundação Ezequiel Dias
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T18:43:14Z
dc.date.issued2023-10-01
dc.description.abstractPhospholipases A2 (PLA2s) are main components of snake venoms. Several snake species possess endogenous PLA2 inhibitors in their circulating blood, which are generally known as sbPLIs (an acronym for snake blood phospholipase A2 inhibitors). The sbPLIs are categorized in three classes (alpha, beta or gamma) depending on the existence of distinguishing protein domains in their structure. The Crotalus durrissus terrificus venom has a highly neurotoxic PLA2 - crotoxin (CTX) - in its composition and the self-protection of the snake is mainly ensured by a sbγPLI named CNF (standing for Crotalus neutralizing factor). In an attempt to find smaller molecules able to inhibit the catalytic activity of CTX, in the present study we used linear peptide arrays to identify CNF segments possibly involved in the interaction with the toxin. Five reacting segments were identified as possible interacting regions. The target peptides were synthesized and located in the in silico CNF structure. Although all of them are exposed to the solvent, high concentrations were needed to inhibit the PLA2 activity of the whole venom or CTX. Limitations of the methodology employed and particular characteristics of CTX inhibition by CNF are discussed.en
dc.description.affiliationDiretoria de Pesquisa e Desenvolvimento Fundação Ezequiel Dias, Minas Gerais
dc.description.affiliationDepartamento de Biofísica e Farmacologia Instituto de Biociências Universidade Estadual Paulista (UNESP), Botucatu
dc.description.affiliationInstituto de Estudos Avançados do Mar (IEAMar) Universidade Estadual Paulista (UNESP), São Vicente
dc.description.affiliationUnespDepartamento de Biofísica e Farmacologia Instituto de Biociências Universidade Estadual Paulista (UNESP), Botucatu
dc.description.affiliationUnespInstituto de Estudos Avançados do Mar (IEAMar) Universidade Estadual Paulista (UNESP), São Vicente
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.identifierhttp://dx.doi.org/10.1016/j.toxicon.2023.107267
dc.identifier.citationToxicon, v. 234.
dc.identifier.doi10.1016/j.toxicon.2023.107267
dc.identifier.issn1879-3150
dc.identifier.issn0041-0101
dc.identifier.scopus2-s2.0-85172260458
dc.identifier.urihttps://hdl.handle.net/11449/299706
dc.language.isoeng
dc.relation.ispartofToxicon
dc.sourceScopus
dc.subjectCNF
dc.subjectCrotalus
dc.subjectCrotoxin
dc.subjectPhospholipase A2
dc.subjectPhospholipase A2 inhibitor
dc.subjectSPOT synthesis
dc.titleMapping possible interaction sites for crotoxin in CNF, a gamma PLA2 inhibitor from Crotalus durissus terrificus rattle snake, using SPOT synthesisen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationab63624f-c491-4ac7-bd2c-767f17ac838d
relation.isOrgUnitOfPublication.latestForDiscoveryab63624f-c491-4ac7-bd2c-767f17ac838d
unesp.author.orcid0000-0002-9016-8979[2]
unesp.author.orcid0000-0002-4494-5108[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Estudos Avançados do Mar, São Vicentept

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