Combined Peptidomic and Proteomic Analysis of Electrically Stimulated and Manually Dissected Venom from the South American Bullet Ant Paraponera clavata (original) (raw)

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dc.contributor.author Aili, SR en_US
dc.contributor.author Touchard, A en_US
dc.contributor.author Petitclerc, F en_US
dc.contributor.author Dejean, A en_US
dc.contributor.author Orivel, J en_US
dc.contributor.author Padula, MP ORCID badge https://orcid.org/0000-0002-8283-0643 en_US
dc.contributor.author Escoubas, P en_US
dc.contributor.author Nicholson, GM ORCID badge https://orcid.org/0000-0002-4277-4296 en_US
dc.date.issued 2017-03-03 en_US
dc.identifier.citation Journal of Proteome Research, 2017, 16 (3), pp. 1339 - 1351 en_US
dc.identifier.issn 1535-3893 en_US
dc.identifier.uri http://hdl.handle.net/10453/123916
dc.description.abstract © 2017 American Chemical Society. Ants have evolved venoms rich in peptides and proteins used for predation, defense, and communication. However, they remain extremely understudied due to the minimal amount of venom secreted by each ant. The present study investigated the differences in the proteome and peptidome of the venom from the bullet ant, Paraponera clavata. Venom samples were collected from a single colony either by manual venom gland dissection or by electrical stimulation and were compared using proteomic methods. Venom proteins were separated by 2D-PAGE and identified by nanoLC-ESI-QTOF MS/MS. Venom peptides were initially separated using C18 reversed-phase high-performance liquid chromatography, then analyzed by MALDI-TOF MS. The proteomic analysis revealed numerous proteins that could be assigned a biological function (total 94), mainly as toxins, or roles in cell regulation and transport. This investigation found that ca. 73% of the proteins were common to venoms collected by the two methods. The peptidomic analysis revealed a large number of peptides (total 309) but with <20% shared by the two collection methods. There was also a marked difference between venoms obtained by venom gland dissection from different ant colonies. These findings demonstrate the rich composition and variability of P. clavata venom. en_US
dc.relation.ispartof Journal of Proteome Research en_US
dc.relation.isbasedon 10.1021/acs.jproteome.6b00948 en_US
dc.subject.classification Biochemistry & Molecular Biology en_US
dc.subject.mesh Animals en_US
dc.subject.mesh Ants en_US
dc.subject.mesh Peptides en_US
dc.subject.mesh Insect Proteins en_US
dc.subject.mesh Ant Venoms en_US
dc.subject.mesh Electrophoresis, Gel, Two-Dimensional en_US
dc.subject.mesh Proteomics en_US
dc.subject.mesh Tandem Mass Spectrometry en_US
dc.title Combined Peptidomic and Proteomic Analysis of Electrically Stimulated and Manually Dissected Venom from the South American Bullet Ant Paraponera clavata en_US
dc.type Journal Article
utslib.citation.volume 3 en_US
utslib.citation.volume 16 en_US
utslib.for 0601 Biochemistry and Cell Biology en_US
utslib.for 0301 Analytical Chemistry en_US
utslib.for 03 Chemical Sciences en_US
utslib.for 06 Biological Sciences en_US
pubs.embargo.period Not known en_US
pubs.organisational-group /University of Technology Sydney
pubs.organisational-group /University of Technology Sydney/Faculty of Science
pubs.organisational-group /University of Technology Sydney/Faculty of Science/School of Life Sciences
pubs.organisational-group /University of Technology Sydney/Strength - CHT - Health Technologies
utslib.copyright.status open_access
pubs.issue 3 en_US
pubs.publication-status Published en_US
pubs.volume 16 en_US