Schittmayer Matthias, Fritz Katarina, Liesinger Laura, Griss Johannes, Birner-Gruenberger Ruth
Research Unit Functional Proteomics and Metabolic Pathways, Institute of Pathology, Medical University of Graz , 8010 Graz, Austria.
Omics Center Graz, BioTechMed-Graz , 8010 Graz, Austria.
J Proteome Res. 2016 Apr 1;15(4):1222-9. doi: 10.1021/acs.jproteome.5b01105. Epub 2016 Mar 22.
Chemically modified trypsin is a standard reagent in proteomics experiments but is usually not considered in database searches. Modification of trypsin is supposed to protect the protease against autolysis and the resulting loss of activity. Here, we show that modified trypsin is still subject to self-digestion, and, as a result, modified trypsin-derived peptides are present in standard digests. We depict that these peptides commonly lead to false-positive assignments even if native trypsin is considered in the database. Moreover, we present an easily implementable method to include modified trypsin in the database search with a minimal increase in search time and search space while efficiently avoiding these false-positive hits.
化学修饰的胰蛋白酶是蛋白质组学实验中的标准试剂,但在数据库搜索中通常未被考虑。胰蛋白酶的修饰旨在保护蛋白酶不发生自溶并避免由此导致的活性丧失。在此,我们表明修饰后的胰蛋白酶仍会发生自我消化,因此,标准消化物中存在修饰胰蛋白酶衍生的肽段。我们描述了即使在数据库中考虑了天然胰蛋白酶,这些肽段通常也会导致假阳性匹配。此外,我们提出了一种易于实施的方法,可将修饰的胰蛋白酶纳入数据库搜索,同时搜索时间和搜索空间的增加最小,且能有效避免这些假阳性匹配。