Oral Sessions
(Day1, Day2, Day3, Day4)
Poster Presentations
(Day1, Day2, Day3, Day4)
Luncheon Seminars
(Day1, Day2, Day3, Day4)
Poster Presentations
- Day 1, May 15(Tue.) Poster
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1P-01 PDF
A novel and simple database search strategy to prevent false-positive identification by using a spectral library of unexpected peptides from chemically modified trypsin
Chemically modified trypsin by reductive methylation is a standard reagent in protein identification by mass spectrometry. The reductive methylation of trypsin is supposed to protect the enzyme against autolysis. However, it has been reported that peptides with mono- or di-methylated Lys, or Asn residue at their C-termini were observed in autolysis products of chemically modified trypsin. In most cases, the chemical modification of trypsin is not considered in database searches. Modified trypsin-derived spectral data might be incorrectly assigned to peptides of other proteins, making false-positive identification. In this paper, we will present a novel and simple database search strategy to prevent false-positive identification by using a spectral library of unexpected peptides from chemically modified trypsin.