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A rapid and accurate approach for Prediction of interactomes from co-elution data (PrInCE)

View ORCID ProfileR. Greg Stacey, Michael A. Skinnider, Nichollas E. Scott, Leonard J. Foster
doi: https://doi.org/10.1101/152355
R. Greg Stacey
1Michael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, Canada
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  • ORCID record for R. Greg Stacey
  • For correspondence: richard.greg.stacey@ubc.msl.ca foster@msl.ubc.ca
Michael A. Skinnider
1Michael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, Canada
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Nichollas E. Scott
1Michael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, Canada
2Doherty Institute, University of Melbourne, Melbourne, Australia
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Leonard J. Foster
1Michael Smith Laboratories, University of British Columbia, Vancouver, V6T 1Z4, Canada
3Department of Biochemistry, University of British Columbia, Vancouver, V6T 1Z3, Canada.
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  • For correspondence: richard.greg.stacey@ubc.msl.ca foster@msl.ubc.ca
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Abstract

Background An organism’s protein interactome, or complete network of protein-protein interactions, defines the protein complexes that drive cellular processes. Techniques for studying protein complexes have traditionally applied targeted strategies such as yeast two-hybrid or affinity purification-mass spectrometry to assess protein interactions. However, given the vast number of protein complexes, more scalable methods are necessary to accelerate interaction discovery and to construct whole interactomes. We recently developed a complementary technique based on the use of protein correlation profiling (PCP) and stable isotope labeling in amino acids in cell culture (SILAC) to assess chromatographic co-elution as evidence of interacting proteins. Importantly, PCP-SILAC is also capable of measuring protein interactions simultaneously under multiple biological conditions, allowing the detection of treatment-specific changes to an interactome. Given the uniqueness and high dimensionality of co-elution data, new tools are needed to compare protein elution profiles, control false discovery rates, and construct an accurate interactome.

Results Here we describe a freely available bioinformatics pipeline, PrInCE, for the analysis of co-elution data. PrInCE is a modular, open-source library that is computationally inexpensive, able to use label and label-free data, and capable of detecting tens of thousands of protein-protein interactions. Using a machine learning approach, PrInCE offers greatly reduced run time, better performance, prediction of protein complexes, and greater ease of use over previous bioinformatics tools for co-elution data. PrInCE is implemented in Matlab (version R2015b). Source code and standalone executable programs for Windows and Mac OSX are available at https://github.com/fosterlab/PrInCE, where usage instructions can be found. An example dataset and output are also provided for testing purposes.

Conclusions PrInCE is the first fast and easy-to-use data analysis pipeline that predicts interactomes and protein complexes from co-elution data. PrInCE allows researchers without bioinformatics proficiency to analyze high-throughput co-elution datasets.

Footnotes

  • Abbreviations
    PrInCE
    Predicting interactomes from co-elution
    PCP
    Protein correlation profiling
    SILAC
    Stable isotope labelling by amino acids in cell culture
    Y2H
    Yeast two-hybrid
    AP-MS
    Affinity purification mass spectrometry
    PPI
    Protein-protein interaction

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted June 20, 2017.
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A rapid and accurate approach for Prediction of interactomes from co-elution data (PrInCE)
R. Greg Stacey, Michael A. Skinnider, Nichollas E. Scott, Leonard J. Foster
bioRxiv 152355; doi: https://doi.org/10.1101/152355
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A rapid and accurate approach for Prediction of interactomes from co-elution data (PrInCE)
R. Greg Stacey, Michael A. Skinnider, Nichollas E. Scott, Leonard J. Foster
bioRxiv 152355; doi: https://doi.org/10.1101/152355

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