Maximum Entropy Reconstructions of Dynamic Signaling Networks from Quantitative Proteomics Data

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Maximum Entropy Reconstructions of Dynamic Signaling Networks from Quantitative Proteomics Data

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Title: Maximum Entropy Reconstructions of Dynamic Signaling Networks from Quantitative Proteomics Data
Author: Wolf-Yadlin, Alejandro; Nussinov, Ruth; Locasale, Jason Wei

Note: Order does not necessarily reflect citation order of authors.

Citation: Locasale, Jason W., and Alejandro Wolf-Yadlin. 2009. Maximum entropy reconstructions of dynamic signaling networks from quantitative proteomics data. PLoS ONE 4(8): e6522.
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Abstract: Advances in mass spectrometry among other technologies have allowed for quantitative, reproducible, proteome-wide measurements of levels of phosphorylation as signals propagate through complex networks in response to external stimuli under different conditions. However, computational approaches to infer elements of the signaling network strictly from the quantitative aspects of proteomics data are not well established. We considered a method using the principle of maximum entropy to infer a network of interacting phosphotyrosine sites from pairwise correlations in a mass spectrometry data set and derive a phosphorylation-dependent interaction network solely from quantitative proteomics data. We first investigated the applicability of this approach by using a simulation of a model biochemical signaling network whose dynamics are governed by a large set of coupled differential equations. We found that in a simulated signaling system, the method detects interactions with significant accuracy. We then analyzed a growth factor mediated signaling network in a human mammary epithelial cell line that we inferred from mass spectrometry data and observe a biologically interpretable, small-world structure of signaling nodes, as well as a catalog of predictions regarding the interactions among previously uncharacterized phosphotyrosine sites. For example, the calculation places a recently identified tumor suppressor pathway through ARHGEF7 and Scribble, in the context of growth factor signaling. Our findings suggest that maximum entropy derived network models are an important tool for interpreting quantitative proteomics data.
Published Version: doi:10.1371/journal.pone.0006522
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2728537/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:4633210

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