| Literature DB >> 29578715 |
Stefan K Solntsev, Michael R Shortreed, Brian L Frey, Lloyd M Smith.
Abstract
Correct identification of protein post-translational modifications (PTMs) is crucial to understanding many aspects of protein function in biological processes. G-PTM-D is a recently developed technique for global identification and localization of PTMs. Spectral file calibration prior to applying G-PTM-D, and algorithmic enhancements in the peptide database search significantly increase the accuracy, speed, and scope of PTM identification. We enhance G-PTM-D by using multinotch searches and demonstrate its effectiveness in identification of numerous types of PTMs including high-mass modifications such as glycosylations. The changes described in this work lead to a 20% increase in the number of identified modifications and an order of magnitude decrease in search time. The complete workflow is implemented in MetaMorpheus, a software tool that integrates the database search procedure, identification of coisolated peptides, spectral calibration, and the enhanced G-PTM-D workflow. Multinotch searches are also shown to be useful in contexts other than G-PTM-D by producing superior results when used instead of standard narrow-window and open database searches.Keywords: G-PTM-D; calibration; coisolation; database search; post-translational modification; post-translational modification discovery; proteomics
Mesh:
Year: 2018 PMID: 29578715 DOI: 10.1021/acs.jproteome.7b00873
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466