Please use this identifier to cite or link to this item: https://doi.org/10.1021/pr201185r
Title: SAINT-MS1: Protein-protein interaction scoring using label-free intensity data in affinity purification-mass spectrometry experiments
Authors: Choi, H. 
Glatter, T.
Gstaiger, M.
Nesvizhskii, A.I.
Keywords: affinity purification
intensity
interaction scoring
mass spectrometry
protein-protein interaction
spectral counts
Issue Date: 6-Apr-2012
Citation: Choi, H., Glatter, T., Gstaiger, M., Nesvizhskii, A.I. (2012-04-06). SAINT-MS1: Protein-protein interaction scoring using label-free intensity data in affinity purification-mass spectrometry experiments. Journal of Proteome Research 11 (4) : 2619-2624. ScholarBank@NUS Repository. https://doi.org/10.1021/pr201185r
Abstract: We present a statistical method SAINT-MS1 for scoring protein-protein interactions based on the label-free MS1 intensity data from affinity purification-mass spectrometry (AP-MS) experiments. The method is an extension of Significance Analysis of INTeractome (SAINT), a model-based method previously developed for spectral count data. We reformulated the statistical model for log-transformed intensity data, including adequate treatment of missing observations, that is, interactions identified in some but not all replicate purifications. We demonstrate the performance of SAINT-MS1 using two recently published data sets: a small LTQ-Orbitrap data set with three replicate purifications of single human bait protein and control purifications and a larger drosophila data set targeting insulin receptor/target of rapamycin signaling pathway generated using an LTQ-FT instrument. Using the drosophila data set, we also compare and discuss the performance of SAINT analysis based on spectral count and MS1 intensity data in terms of the recovery of orthologous and literature-curated interactions. Given rapid advances in high mass accuracy instrumentation and intensity-based label-free quantification software, we expect that SAINT-MS1 will become a useful tool allowing improved detection of protein interactions in label-free AP-MS data, especially in the low abundance range. © 2012 American Chemical Society.
Source Title: Journal of Proteome Research
URI: http://scholarbank.nus.edu.sg/handle/10635/108799
ISSN: 15353893
DOI: 10.1021/pr201185r
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