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. 2015 Dec 2;7(12):5236–5253. doi: 10.3390/toxins7124875

Figure 3.

Figure 3

Chromatograms of the MRM signal intensities derived from the y8 ions of the analyte decapeptides from tryptic digests of human serum showing no matrix interference with the y8 ion of the analyte decapeptides from Stx1 and Stx2 subtypes. The signals corresponding to the y8 ion of the analyte decapeptides from Stx1 (YNDDDTFTVK, YNDDDSFTVK, or YNDDDTFTAK); or Stx2a and Stx2f (YNEDDTFTVK); Stx2b, Stx2c, or Stx2d, (YNENDTFTVK); Stx2g (YNGDDTFTVK) or Stx2e (YNEDNTFTVK) are shown in each graph (i). Each sample was spiked with the corresponding 15N-labeled internal standard (ii). The signals for the y8 ions from the corresponding 15N-labeled internal standards (ii) are normalized to 500 to allow the signal from the analyte decapeptide to be viewed on the same plot. The other signals are not normalized.