Table 2 |
||||
|
Improved Peptide Sequence Assignment via De-isotoped MS/MS Spectra. |
||||
|
Experiment |
# Peptides Before Deisotoping |
# Peptides After Deisotoping |
# New Peptides |
% New Peptides |
|
|
||||
|
1 |
218 |
271 |
53 |
31% |
|
|
||||
|
2 |
178 |
208 |
30 |
17% |
|
|
||||
|
3 |
204 |
250 |
46 |
33% |
|
|
||||
|
4 |
379 |
442 |
63 |
34% |
|
|
||||
|
5 |
320 |
391 |
71 |
35% |
|
|
||||
|
Average |
259.8 |
312.4 |
52.6 |
30% |
|
|
||||
|
High resolution Orbitrap HCD MS/MS spectra of high charge state (z > 2+) precursors were frequently not assigned to a peptide sequence due to the presence of multiple isotope peaks per fragment ion. We processed the peak lists (MGF format) using an .mz script to only retain mono-isotopic and singly charged fragment ion peaks. Subsequent research of these data provided an average increase of 30% in the number of high-confidence (Mascot score > 30) peptide assignments across 5 LC-MS runs. |
||||
|
Parikh et al. BMC Bioinformatics 2009 10:364 doi:10.1186/1471-2105-10-364 |
||||