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Structural and functional characterization of two novel peptide toxins isolated from the venom of the social wasp Polybia paulista

dc.contributor.authorSouza, B. M.
dc.contributor.authorMendes, M. A.
dc.contributor.authorSantos, L. D.
dc.contributor.authorMarques, M. R.
dc.contributor.authorCesar, LMM
dc.contributor.authorAlmeida, RNA
dc.contributor.authorPagnocca, F. C.
dc.contributor.authorKonno, K.
dc.contributor.authorPalma, Mario Sergio [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionInstitute Butantan
dc.date.accessioned2014-05-20T13:54:38Z
dc.date.available2014-05-20T13:54:38Z
dc.date.issued2005-11-01
dc.description.abstractTwo novel inflammatory peptides were isolated from the venom of the social wasp Polybia paulista. They had their molecular masses determined by ESI-MS and their primary sequences were elucidated by Edman degradation chemistry as:Polybia-MPI: I D W K K L L D A A K Q I L-NH2 (1654.09 Da),Polybia-CP: I L G T I L G L L K S L-NH2 (1239.73 Da).Both peptides were functionally characterized by using Wistar rat cells. Polybia-MPI is a mast cell lytic peptide, which causes no hemolysis to rat erythrocytes and presents chemotaxis for polymorphonucleated leukocytes (PMNL) and with potent antimicrobial action both against Gram-positive and Gram-negative bacteria. Polybia-CP was characterized as a chemotactic peptide for PMNL cells, presenting antimicrobial action against Gram-positive bacteria, but causing no hemolysis to rat erythrocytes and no mast cell degranulation activity at physiological concentrations. (c) 2005 Elsevier B.V. All rights reserved.en
dc.description.affiliationUNESP, CEIS, Dept Biol,IBRC,CAT CEPID FAPESP, Inst Immunol Invest,Millennium Inst,MCT CNPq, BR-13506900 Rio Claro, SP, Brazil
dc.description.affiliationUNESP, IBRC, Dept Biochem & Microbiol, Rio Claro, SP, Brazil
dc.description.affiliationFAPESP, CAT, CEPID, Inst Butantan, São Paulo, Brazil
dc.description.affiliationUnespUNESP, CEIS, Dept Biol,IBRC,CAT CEPID FAPESP, Inst Immunol Invest,Millennium Inst,MCT CNPq, BR-13506900 Rio Claro, SP, Brazil
dc.description.affiliationUnespUNESP, IBRC, Dept Biochem & Microbiol, Rio Claro, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.format.extent2157-2164
dc.identifierhttp://dx.doi.org/10.1016/j.peptides.2005.04.026
dc.identifier.citationPeptides. New York: Elsevier B.V., v. 26, n. 11, p. 2157-2164, 2005.
dc.identifier.doi10.1016/j.peptides.2005.04.026
dc.identifier.issn0196-9781
dc.identifier.lattes8302605179522059
dc.identifier.lattes2901888624506535
dc.identifier.urihttp://hdl.handle.net/11449/19558
dc.identifier.wosWOS:000233373100016
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofPeptides
dc.relation.ispartofjcr2.851
dc.relation.ispartofsjr1,001
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectPolybia paulistapt
dc.subjecthymenoptera insectpt
dc.subjectpolycationic peptidept
dc.subjectwasp venompt
dc.subjectmastoparanspt
dc.subjectchemotactic peptidespt
dc.titleStructural and functional characterization of two novel peptide toxins isolated from the venom of the social wasp Polybia paulistaen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.lattes8302605179522059[7]
unesp.author.lattes2901888624506535
unesp.author.orcid0000-0002-2078-9286[2]
unesp.author.orcid0000-0001-5832-1825[3]
unesp.author.orcid0000-0002-7363-8211[9]
unesp.author.orcid0000-0002-5026-1933[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Rio Claropt
unesp.departmentBiologia - IBpt
unesp.departmentBioquímica e Microbiologia - IBpt

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