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Elapid Snake Venom Analyses Show the Specificity of the Peptide Composition at the Level of Genera Naja and Notechis

dc.contributor.authorMunawar, Aisha
dc.contributor.authorTrusch, Maria
dc.contributor.authorGeorgieva, Dessislava
dc.contributor.authorHildebrand, Diana
dc.contributor.authorKwiatkowski, Marcel
dc.contributor.authorBehnken, Henning
dc.contributor.authorHarder, Soenke
dc.contributor.authorArni, Raghuvir [UNESP]
dc.contributor.authorSpencer, Patrick
dc.contributor.authorSchlueter, Hartmut
dc.contributor.authorBetzel, Christian
dc.contributor.institutionUniv Hamburg
dc.contributor.institutionUniv Engn & Technol
dc.contributor.institutionUniv Med Ctr Hamburg Eppendorf UKE
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionInstituto de Pesquisas Energéticas e Nucleares (IPEN)
dc.date.accessioned2014-12-03T13:11:08Z
dc.date.available2014-12-03T13:11:08Z
dc.date.issued2014-03-01
dc.description.abstractElapid snake venom is a highly valuable, but till now mainly unexplored, source of pharmacologically important peptides. We analyzed the peptide fractions with molecular masses up to 10 kDa of two elapid snake venoms-that of the African cobra, N. m. mossambica (genus Naja), and the Peninsula tiger snake, N. scutatus, from Kangaroo Island (genus Notechis). A combination of chromatographic methods was used to isolate the peptides, which were characterized by combining complimentary mass spectrometric techniques. Comparative analysis of the peptide compositions of two venoms showed specificity at the genus level. Three-finger (3-F) cytotoxins, bradykinin-potentiating peptides (BPPs) and a bradykinin inhibitor were isolated from the Naja venom. 3-F neurotoxins, Kunitz/basic pancreatic trypsin inhibitor (BPTI)-type inhibitors and a natriuretic peptide were identified in the N. venom. The inhibiting activity of the peptides was confirmed in vitro with a selected array of proteases. Cytotoxin 1 (P01467) from the Naja venom might be involved in the disturbance of cellular processes by inhibiting the cell 20S-proteasome. A high degree of similarity between BPPs from elapid and viperid snake venoms was observed, suggesting that these molecules play a key role in snake venoms and also indicating that these peptides were recruited into the snake venom prior to the evolutionary divergence of the snakes.en
dc.description.affiliationUniv Hamburg, Inst Biochem & Mol Biol, Lab Struct Biol Infect & Inflammat, DESY, D-22603 Hamburg, Germany
dc.description.affiliationUniv Engn & Technol, Dept Chem, Lahore 54890, Pakistan
dc.description.affiliationUniv Hamburg, Inst Organ Chem, D-20146 Hamburg, Germany
dc.description.affiliationUniv Med Ctr Hamburg Eppendorf UKE, Inst Clin Chem, D-20246 Hamburg, Germany
dc.description.affiliationIBILCE UNESP, Dept Phys, BR-15054000 Sao Jose Do Rio Preto, SP, Brazil
dc.description.affiliationInst Pesquisas Energet & Nucl, Ctr Biotecnol, BR-05508000 Sao Paulo, Brazil
dc.description.affiliationUnespIBILCE UNESP, Dept Phys, BR-15054000 Sao Jose Do Rio Preto, SP, Brazil
dc.description.sponsorshipDeutsche Forschungsgemeinschaft
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipHigher Education Commission of Pakistan
dc.description.sponsorshipGerman Academic Exchange Service (DAAD), Germany
dc.description.sponsorshipAlexander von Humboldt Foundation
dc.description.sponsorshipIdDeutsche ForschungsgemeinschaftBE 1443-18-1
dc.description.sponsorshipIdDeutsche Forschungsgemeinschaft26-1
dc.description.sponsorshipIdAlexander von Humboldt Foundation3.3-BUL/1073481 STP
dc.format.extent850-868
dc.identifierhttp://dx.doi.org/10.3390/toxins6030850
dc.identifier.citationToxins. Basel: Mdpi Ag, v. 6, n. 3, p. 850-868, 2014.
dc.identifier.doi10.3390/toxins6030850
dc.identifier.fileWOS000335755700005.pdf
dc.identifier.issn2072-6651
dc.identifier.lattes9162508978945887
dc.identifier.orcid0000-0003-2460-1145
dc.identifier.urihttp://hdl.handle.net/11449/112895
dc.identifier.wosWOS:000335755700005
dc.language.isoeng
dc.publisherMdpi Ag
dc.relation.ispartofToxins
dc.relation.ispartofjcr3.273
dc.relation.ispartofsjr0,955
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectnatriuretic peptidesen
dc.subjectNotechis scutatus from Kangaroo Islanden
dc.subjectNaja mossambica mossambicaen
dc.subjectSnake venomen
dc.subjectpharmacologically active peptidesen
dc.subjectBradykinin potentiating peptidesen
dc.subjectKunitz-type inhibitoren
dc.subjectneurotoxinen
dc.subjectcytotoxinen
dc.titleElapid Snake Venom Analyses Show the Specificity of the Peptide Composition at the Level of Genera Naja and Notechisen
dc.typeArtigo
dcterms.rightsHolderMdpi Ag
dspace.entity.typePublication
unesp.author.lattes9162508978945887[8]
unesp.author.orcid0000-0003-2460-1145[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt
unesp.departmentFísica - IBILCEpt

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