Figure 1
From: Venom composition and pain-causing toxins of the Australian great carpenter bee Xylocopa aruana

The venom composition of X. aruana. (a) Adult female X. aruana (the specimen that was used in this study). (b) Total ion chromatogram from LC–MS/MS analysis of X. aruana venom with peaks corresponding to identified venom peptides labelled. Additional proteins were detected in the reduced, alkylated and trypsin-digested venom sample. The signal corresponding to XYTX1-Xa1a is saturated. Asterisks mark derivatives of XYTX1-Xa1a. (c) Complete CID-MS/MS spectrum of the [M + 4H]+4 precursor ion of XYTX1-Xa1a. Inset: [M + 4H]+4 MS spectrum (theoretical [M + 4H]+4 = 483.075). (d) Complete CID-MS/MS spectrum of the [M + 6H]+6 precursor ion of XYTX2-Xa2a (in the reduced and alkylated venom sample). Inset: [M + 6H]+6 MS spectrum (theoretical [M + 6H]+6 = 449.734). b-, y- and internal ions (#) are labelled (for clarity, other ions are not labelled). Inset: MS spectrum. (e) Venom component-encoding transcripts (i.e., those encoding peptides detected in the venom by MS) comprised 74.1% of total transcript expression. Of these, transcripts encoding XYTX1-Xa1a, XYTX2-Xa2a, PLA2, and other venom proteins comprised 93.4, 3.0, 3.4, and 0.2%, respectively, of venom component expression. (f) Venom component-encoding transcripts (highlighted in yellow) are found exclusively in the highly expressed portion of the venom apparatus transcriptome. TPM transcripts per million.