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Design of bioactive peptides derived from CART sequence isolated from the toadfish Thalassophryne nattereri

dc.contributor.authorConceição, Katia
dc.contributor.authorde Cena, Gabrielle L.
dc.contributor.authorda Silva, Verônica A.
dc.contributor.authorde Oliveira Neto, Xisto Antonio
dc.contributor.authorde Andrade, Vitor Martins
dc.contributor.authorTada, Dayane Batista
dc.contributor.authorRichardson, Michael
dc.contributor.authorde Andrade, Sonia A.
dc.contributor.authorDias, Susana
dc.contributor.authorCastanho, Miguel A. R. B.
dc.contributor.authorLopes-Ferreira, Mônica
dc.date.accessioned2023-04-21T13:51:34Z
dc.date.available2023-04-21T13:51:34Z
dc.date.issued2020
dc.description© King Abdulaziz City for Science and Technology 2020pt_PT
dc.description.abstractThe emergence of bacterial resistance due to the indiscriminate use of antibiotics warrants the need for developing new bioactive agents. In this context, antimicrobial peptides are highly useful for managing resistant microbial strains. In this study, we report the isolation and characterization of peptides obtained from the venom of the toadfish Thalassophryne nattereri. These peptides were active against Gram-positive and Gram-negative bacteria and fungi. The primary amino acid sequences showed similarity to Cocaine and Amphetamine Regulated Transcript peptides, and two peptide analogs—Tn CRT2 and Tn CRT3—were designed using the AMPA algorithm based on these sequences. The analogs were subjected to physicochemical analysis and antimicrobial screening and were biologically active at concentrations ranging from 2.1 to 13 μM. Zeta potential analysis showed that the peptide analogs increased the positive charge on the cell surface of Grampositive and Gram-negative bacteria. The toxicity of Tn CRT2 and Tn CRT3 were analyzed in vitro using a hemolytic assay and tetrazolium salt reduction in fibroblasts and was found to be significant only at high concentrations (up to 40 μM). These results suggest that this methodological approach is appropriate to design novel antimicrobial peptides to fight bacterial infections and represents a new and promising discovery in fish venom.pt_PT
dc.description.sponsorshipThis research was supported by FAPESP grant No. 2017/00032-0.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citation3 Biotech 10, 162 (2020)pt_PT
dc.identifier.doi10.1007/s13205-020-2151-4pt_PT
dc.identifier.eissn2190-5738
dc.identifier.issn2190-572X
dc.identifier.urihttp://hdl.handle.net/10451/57225
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSpringerpt_PT
dc.relation.publisherversionhttps://www.springer.com/journal/13205pt_PT
dc.subjectThalassophryne nattereript_PT
dc.subjectVenompt_PT
dc.subjectAntimicrobial peptidept_PT
dc.subjectCytotoxicitypt_PT
dc.titleDesign of bioactive peptides derived from CART sequence isolated from the toadfish Thalassophryne nattereript_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.issue4pt_PT
oaire.citation.startPage162pt_PT
oaire.citation.title3 Biotechpt_PT
oaire.citation.volume10pt_PT
person.familyNameDias
person.familyNameCastanho
person.givenNameSusana
person.givenNameMiguel
person.identifier.ciencia-idF61D-0A28-659A
person.identifier.orcid0000-0001-8910-5404
person.identifier.orcid0000-0001-7891-7562
person.identifier.scopus-author-id56605575600
rcaap.rightsrestrictedAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication6b2869fd-0474-4f6c-bf5d-5973ee423da7
relation.isAuthorOfPublicationf5e46f85-fabf-450a-9ee2-1c7b59410892
relation.isAuthorOfPublication.latestForDiscoveryf5e46f85-fabf-450a-9ee2-1c7b59410892

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