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A multi-protease, multi-dissociation, bottom-up-to-top-down proteomic view of the Loxosceles intermedia venom.
Trevisan-Silva, Dilza; Bednaski, Aline V; Fischer, Juliana S G; Veiga, Silvio S; Bandeira, Nuno; Guthals, Adrian; Marchini, Fabricio K; Leprevost, Felipe V; Barbosa, Valmir C; Senff-Ribeiro, Andrea; Carvalho, Paulo C.
Affiliation
  • Trevisan-Silva D; Department of Cell Biology, Federal University of Paraná, Curitiba 81531-980, Brazil.
  • Bednaski AV; Department of Cell Biology, Federal University of Paraná, Curitiba 81531-980, Brazil.
  • Fischer JSG; Computational Mass Spectrometry &Proteomics Group, Carlos Chagas Institute, Fiocruz, Curitiba 81.350-010, Brazil.
  • Veiga SS; Department of Cell Biology, Federal University of Paraná, Curitiba 81531-980, Brazil.
  • Bandeira N; Center for Computational Mass Spectrometry, University of California, San Diego 92093-0404, USA.
  • Guthals A; Center for Computational Mass Spectrometry, University of California, San Diego 92093-0404, USA.
  • Marchini FK; Functional Genomics Laboratory, Carlos Chagas Institute, Fiocruz, Curitiba 81.350-010, Brazil.
  • Leprevost FV; Mass Spectrometry Facility RPT02H, Carlos Chagas Institute, Fiocruz, Curitiba 81.350-010, Brazil.
  • Barbosa VC; Computational Mass Spectrometry &Proteomics Group, Carlos Chagas Institute, Fiocruz, Curitiba 81.350-010, Brazil.
  • Senff-Ribeiro A; Systems Engineering and Computer Science Program, COPPE, Federal University of Rio de Janeiro, Rio de Janeiro 21941-914, Brazil.
  • Carvalho PC; Department of Cell Biology, Federal University of Paraná, Curitiba 81531-980, Brazil.
Sci Data ; 4: 170090, 2017 07 11.
Article in En | MEDLINE | ID: mdl-28696408
ABSTRACT
Venoms are a rich source for the discovery of molecules with biotechnological applications, but their analysis is challenging even for state-of-the-art proteomics. Here we report on a large-scale proteomic assessment of the venom of Loxosceles intermedia, the so-called brown spider. Venom was extracted from 200 spiders and fractioned into two aliquots relative to a 10 kDa cutoff mass. Each of these was further fractioned and digested with trypsin (4 h), trypsin (18 h), pepsin (18 h), and chymotrypsin (18 h), then analyzed by MudPIT on an LTQ-Orbitrap XL ETD mass spectrometer fragmenting precursors by CID, HCD, and ETD. Aliquots of undigested samples were also analyzed. Our experimental design allowed us to apply spectral networks, thus enabling us to obtain meta-contig assemblies, and consequently de novo sequencing of practically complete proteins, culminating in a deep proteome assessment of the venom. Data are available via ProteomeXchange, with identifier PXD005523.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spider Venoms / Spiders / Proteome Type of study: Prognostic_studies Limits: Animals Language: En Journal: Sci Data Year: 2017 Document type: Article Affiliation country: Brazil

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spider Venoms / Spiders / Proteome Type of study: Prognostic_studies Limits: Animals Language: En Journal: Sci Data Year: 2017 Document type: Article Affiliation country: Brazil