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dc.contributor.authorReverté, Jaume
dc.contributor.authorAlkassar, Mounira
dc.contributor.authorRambla Alegre, Maria
dc.contributor.authorSanchez Henao, Julian Andres
dc.contributor.authorMandalakis, Manolis
dc.contributor.authorParisteraki, Panagiota
dc.contributor.authorSureda, Francesc X.
dc.contributor.authorDiogène, Jorge
dc.contributor.authorCampàs, Mònica
dc.contributor.otherProducció Animalca
dc.date.accessioned2025-12-18T10:17:59Z
dc.date.available2025-12-18T10:17:59Z
dc.date.issued2025-12-10
dc.identifier.issn0009-2797ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/4911
dc.description.abstractTetrodotoxins (TTXs) pose significant food safety risks due to their potent neurotoxicity. Growing concerns about the impact of these toxins on public health have driven the development of new detection methods, with immunoassays showing strong potential. However, limited knowledge of the cross-reactivity of anti-TTX antibodies with analogues may compromise the reliability of these assays in food safety applications. To address this, cross-reactivity factors (CRFs) for five TTX analogues (i.e., 11-norTTX-6(S)-ol, 11-deoxyTTX, 6,11-dideoxyTTX, 5,11-dideoxyTTX, and 5,6,11-trideoxyTTX) were assessed using a magnetic bead-based immunoassay. In parallel, the antibody's ability to neutralise the toxicity of TTX analogues was evaluated in Neuro-2a cells using automated patch clamp, a single-cell biosensing platform specifically designed for in vitro toxicity assessment and characterisation. Antibody cross-reactivity towards the tested analogues correlated with their relative toxicity, enabling a selective detection of the most hazardous compounds. These findings highlight the dual role of molecular structure in dictating both toxicological potency and immunological recognition, and support the use of immunoassays as effective tools for TTX monitoring in food safety applications.ca
dc.description.sponsorshipThis research was funded by the Ministerio de Ciencia e Innovación (MICIN) and the Agencia Estatal de Investigación (AEI) (Spain) through the CELLECTRA (PID2020-112976RB-C21 and PID2020-112976RB-C22) and the BiOCEANsing (PID2023-149899OB-C21 and PID2023-149899OB-C22) projects. Jaume Reverté acknowledges IRTA for his PhD grant (CPI0422). Mounira Alkassar acknowledges MICIN and AEI for her PhD grant (PRE2019-088181). Andres Sanchez-Henao acknowledges the Canary Islands Research Agency (ACIISI) for his research staff training aid through the Catalina Ruiz Program (APCR2022010011). The authors also acknowledge the support from CERCA Programme/Generalitat de Catalunya.ca
dc.format.extent10ca
dc.language.isoengca
dc.publisherElsevierca
dc.relation.ispartofChemico-Biological Interactionsca
dc.rightsAttribution 4.0 Internationalca
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleMechanistic insights into antibody recognition of tetrodotoxin analogues: Implications for neurotoxicological assessmentca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.relation.projectIDMICINNPrograma Estatal de generación del conocimiento y fortalecimiento científico y tecnológico del sistema I+D+I y Programa Estatal de I+D+I orientada a los retos de la sociedad/PID2020-112976RB-C21/ES/Herramientas biotecnológicas basadas en células y receptores para la detección de ciguatoxinas y tetrodotoxinas/CELLECTRAca
dc.relation.projectIDMICINN/Programa Estatal de generación del conocimiento y fortalecimiento científico y tecnológico del sistema I+D+I y Programa Estatal de I+D+I orientada a los retos de la sociedad/PID2020-112976RB-C22/ES/Herramientas biotecnológicas basadas en células y aptámeros para la detección de ciguatoxinas y tetrodotoxinas/CELLECTRAca
dc.relation.projectIDMICINN/Programa Estatal para impulsar la investigación científico-técnica y su transferencia/PID2023-149899OB-C21/ES/Tecnologías bio-analíticas basadas en anticuerpos, células y espectrometría de masas para explorar las fronteras de las toxinas marinas/BiOCEANsingca
dc.relation.projectIDMICINN/Programa Estatal para impulsar la investigación científico-técnica y su transferencia/PID2023-149899OB-C22/ES/Tecnologías bio-analíticas basadas en pequeñas proteínas combinatorias, canales iónicos artificiales y células para explorar las fronteras de las toxinas marinas/BiOCEANsingca
dc.subject.udc574ca
dc.identifier.doihttps://doi.org/10.1016/j.cbi.2025.111871ca
dc.contributor.groupAigües Marines i Continentalsca


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