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Cloning and Identification of a Complete cDNA Coding for a Bactericidal and Antitumoral Acidic Phospholipase A(2) from Bothrops jararacussu Venom

dc.contributor.authorRoberto, Patricia G.
dc.contributor.authorKashima, Simone
dc.contributor.authorMarcussi, Silvana
dc.contributor.authorPereira, Jose O.
dc.contributor.authorAstolfi-Filho, Spartaco
dc.contributor.authorNomizo, Auro
dc.contributor.authorGiglio, Jose R.
dc.contributor.authorFontes, Marcos R. M. [UNESP]
dc.contributor.authorSoares, Andreimar M.
dc.contributor.authorFranca, Suzelei C.
dc.contributor.institutionUniv Ribeirao Preto
dc.contributor.institutionUniversidade Federal do Amazonas (UFAM)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:49:25Z
dc.date.available2014-05-20T13:49:25Z
dc.date.issued2004-05-01
dc.description.abstractIn order to better understand the function of acidic phospholipases A(2) (PLA(2)s) from snake venoms, expressed sequence tags (ESTs) that code for acidic PLA(2)s were isolated from a cDNA library prepared from the poly(A) + RNA of venomous glands of Bothrops jararacussu. The complete nucleotide sequence (366 bp), named BOJU-III, encodes the BthA-I-PLA(2) precursor, which includes a signal peptide and the mature protein with 16 and 122 amino acid residues, respectively. Multiple comparison of both the nucleotide and respective deduced amino acid sequence with EST and protein sequences from databases revealed that the full-length cDNA identified (BOJU III - AY145836) is related to an acidic PLA(2) sharing similarity, within the range 55-81%, with acidic phospholipases from snake venoms. Moreover, phylogenetic analysis of amino acid sequences of acidic PLA(2)s from several pit viper genera showed close evolutionary relationships among acidic PLA(2)s from Bothrops, Crotalus, and Trimeresurus. The molecular modeling showed structural similarity with other dimeric class II PLA(2)s from snake venoms. The native protein BthA-I-PLA(2), a nontoxic acidic PLA(2) directly isolated from Bothrops jararacussu snake venom, was purified and submitted to various bioassays. BthA-I-PLA(2) displayed high catalytic activity and induced Ca(2+)-dependent liposome disruption. Edema induced by this PLA(2) was inhibited by indomethacin and dexamethasone, thus suggesting involvement of the cyclo-oxygenase pathway. BthA-I-PLA(2) showed anticoagulant activity upon human plasma and inhibited phospholipid-dependent platelet aggregation induced by collagen or ADP. In addition, it displayed bactericidal activity against Escherichia coli and Staphylococcus aureus and antitumoral effect upon breast adrenocarcinoma as well as upon human leukemia T and Erlich ascitic tumor. Following chemical modification with p-bromophenacyl bromide, total loss of the enzymatic and pharmacological activities were observed. This is the first report on the isolation and identification of a cDNA encoding a complete acidic PLA(2) from Bothrops venom, exhibiting bactericidal and antitumoral effects.en
dc.description.affiliationUniv Ribeirao Preto, UNAERP, Unidade Biotecnol, Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv Fed Amazonas, Fac Ciências Agr, Manaus, Amazonas, Brazil
dc.description.affiliationUniv São Paulo, FCFRP, Dept Anal Clin Toxicol & Bromatol, BR-14049 Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv São Paulo, FMRP, Dept Bioquim & Imunol, BR-14049 Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv Estadual Paulista, IB, Dept Fis & Biofis, Botucatu, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, IB, Dept Fis & Biofis, Botucatu, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipUniversidade de Ribeirao Preto (UNAERP)
dc.format.extent273-285
dc.identifierhttp://dx.doi.org/10.1023/B:JOPC.0000027852.92208.60
dc.identifier.citationProtein Journal. New York: Springer, v. 23, n. 4, p. 273-285, 2004.
dc.identifier.doi10.1023/B:JOPC.0000027852.92208.60
dc.identifier.issn1572-3887
dc.identifier.urihttp://hdl.handle.net/11449/17615
dc.identifier.wosWOS:000208031900005
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofProtein Journal
dc.relation.ispartofjcr1.133
dc.relation.ispartofsjr0,451
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectAcidic phospholipases A(2)pt
dc.subjectantitumoral effectpt
dc.subjectbactericidalpt
dc.subjectBothrops jararacussupt
dc.subjectBPB-chemical modificationpt
dc.subjectcDNApt
dc.subjectstructural analysispt
dc.titleCloning and Identification of a Complete cDNA Coding for a Bactericidal and Antitumoral Acidic Phospholipase A(2) from Bothrops jararacussu Venomen
dc.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
dspace.entity.typePublication
unesp.author.orcid0000-0003-4864-430X[10]
unesp.author.orcid0000-0002-4634-6221[8]
unesp.author.orcid0000-0002-1487-0141[2]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentFísica e Biofísica - IBBpt

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