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. 2021 Jun 14;20(7):3559–3566. doi: 10.1021/acs.jproteome.1c00169

Figure 1.

Figure 1

Mass spectrometry-based de novo sequencing of the monoclonal antibody herceptin. The variable regions of the heavy (A) and light chains (B) are shown. The MS-based sequence is shown alongside the known herceptin sequence, with differences highlighted by asterisks (*). Exemplary MS/MS spectra supporting the assigned sequences of the heavy- and light-chain CDRs are shown below the alignments with protease, precursor charge state, and fragmentation type indicated. Peptide sequence and fragment coverage are indicated on top of the spectra, with b/c ions indicated in blue/teal and y/z ions in red/orange. The same coloring is used to annotate peaks in the spectra, with additional peaks such as intact/charge reduced precursors, neutral losses, and immonium ions indicated in green. Note that to prevent overlapping peak labels, only a subset of successfully matched peaks are annotated.