Motivation: High-throughput protein identification experiments based on tandem mass spectrometry (MS/MS) often suffer from low sensitivity and low-confidence protein identifications. In a typical shotgun proteomics experiment, it is assumed that all proteins are equally likely to be present. However, there is often other evidence to suggest that a protein is present and confidence in individual protein identification can be updated accordingly. Results: We develop a method that analyzes MS/MS experiments in the larger context of the biological processes active in a cell. Our method, MSNet, improves protein identification in shotgun proteomics experiments by considering information on functional associations from a gene functional network. MSNet substantially increases the number of proteins identified in the sample at a given error rate. We identify 8-29% more proteins than the original MS experiment when applied to yeast grown in different experimental conditions analyzed on different MS/MS instruments, and 37% more proteins in a human sample. We validate up to 94% of our identifications in yeast by presence in ground-truth reference sets. © The Author(s) 2009. Published by Oxford University Press.
CITATION STYLE
Ramakrishnan, S. R., Vogel, C., Kwon, T., Penalva, L. O., Marcotte, E. M., & Miranker, D. P. (2009). Mining gene functional networks to improve mass-spectrometry-based protein identification. Bioinformatics, 25(22), 2955–2961. https://doi.org/10.1093/bioinformatics/btp461
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