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Training Signaling Pathway Maps to Biochemical Data with Constrained Fuzzy Logic: Quantitative Analysis of Liver Cell Responses to Inflammatory Stimuli

Overview of attention for article published in PLoS Computational Biology, March 2011
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Title
Training Signaling Pathway Maps to Biochemical Data with Constrained Fuzzy Logic: Quantitative Analysis of Liver Cell Responses to Inflammatory Stimuli
Published in
PLoS Computational Biology, March 2011
DOI 10.1371/journal.pcbi.1001099
Pubmed ID
Authors

Melody K. Morris, Julio Saez-Rodriguez, David C. Clarke, Peter K. Sorger, Douglas A. Lauffenburger

Abstract

Predictive understanding of cell signaling network operation based on general prior knowledge but consistent with empirical data in a specific environmental context is a current challenge in computational biology. Recent work has demonstrated that Boolean logic can be used to create context-specific network models by training proteomic pathway maps to dedicated biochemical data; however, the Boolean formalism is restricted to characterizing protein species as either fully active or inactive. To advance beyond this limitation, we propose a novel form of fuzzy logic sufficiently flexible to model quantitative data but also sufficiently simple to efficiently construct models by training pathway maps on dedicated experimental measurements. Our new approach, termed constrained fuzzy logic (cFL), converts a prior knowledge network (obtained from literature or interactome databases) into a computable model that describes graded values of protein activation across multiple pathways. We train a cFL-converted network to experimental data describing hepatocytic protein activation by inflammatory cytokines and demonstrate the application of the resultant trained models for three important purposes: (a) generating experimentally testable biological hypotheses concerning pathway crosstalk, (b) establishing capability for quantitative prediction of protein activity, and (c) prediction and understanding of the cytokine release phenotypic response. Our methodology systematically and quantitatively trains a protein pathway map summarizing curated literature to context-specific biochemical data. This process generates a computable model yielding successful prediction of new test data and offering biological insight into complex datasets that are difficult to fully analyze by intuition alone.

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Geographical breakdown

Country Count As %
United States 12 4%
United Kingdom 4 1%
Netherlands 2 <1%
Germany 2 <1%
Italy 2 <1%
Switzerland 1 <1%
Brazil 1 <1%
France 1 <1%
Hungary 1 <1%
Other 1 <1%
Unknown 250 90%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 81 29%
Researcher 79 29%
Student > Master 23 8%
Professor > Associate Professor 16 6%
Student > Bachelor 16 6%
Other 43 16%
Unknown 19 7%
Readers by discipline Count As %
Agricultural and Biological Sciences 123 44%
Biochemistry, Genetics and Molecular Biology 43 16%
Engineering 26 9%
Computer Science 19 7%
Medicine and Dentistry 17 6%
Other 25 9%
Unknown 24 9%