You are in the accessibility menu

Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/112895
Full metadata record
DC FieldValueLanguage
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-
dc.contributor.authorSpencer, Patrick-
dc.contributor.authorSchlueter, Hartmut-
dc.contributor.authorBetzel, Christian-
dc.date.accessioned2014-12-03T13:11:08Z-
dc.date.accessioned2016-10-25T20:12:15Z-
dc.date.available2014-12-03T13:11:08Z-
dc.date.available2016-10-25T20:12:15Z-
dc.date.issued2014-03-01-
dc.identifierhttp://dx.doi.org/10.3390/toxins6030850-
dc.identifier.citationToxins. Basel: Mdpi Ag, v. 6, n. 3, p. 850-868, 2014.-
dc.identifier.issn2072-6651-
dc.identifier.urihttp://hdl.handle.net/11449/112895-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/112895-
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.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.format.extent850-868-
dc.language.isoeng-
dc.publisherMdpi Ag-
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.typeoutro-
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.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.sponsorshipIdDeutsche ForschungsgemeinschaftBE 1443-18-1-
dc.description.sponsorshipIdDeutsche Forschungsgemeinschaft26-1-
dc.description.sponsorshipIdAlexander von Humboldt Foundation3.3-BUL/1073481 STP-
dc.identifier.doi10.3390/toxins6030850-
dc.identifier.wosWOS:000335755700005-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000335755700005.pdf-
dc.relation.ispartofToxins-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

There are no files associated with this item.
 

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.