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Integrating Protein Localization with Automated Signaling Pathway Reconstruction

دمج توطين البروتين مع إعادة بناء مسار الإشارات الآلي
Authors: Ibrahim Youssef; Jeffrey Law; Anna Ritz;

Integrating Protein Localization with Automated Signaling Pathway Reconstruction

Abstract

AbstractUnderstanding cellular responses via signal transduction is a core focus in systems biology. Tools to automatically reconstruct signaling pathways from protein-protein interactions (PPIs) can help biologists generate testable hypotheses about signaling. However, automatic reconstruction of signaling pathways suffers from many interactions with the same confidence score leading to many equally good candidates. Further, some reconstructions are biologically misleading due to ignoring protein localization information. We proposeLocPL, a method to improve the automatic reconstruction of signaling pathways from PPIs by incorporating information about protein localization in the reconstructions. The method relies on a dynamic program to ensure that the proteins in a reconstruction are localized in cellular compartments that are consistent with signal transduction from the membrane to the nucleus.LocPLand existing reconstruction algorithms are applied to two PPI networks and assessed using both global and local definitions of accuracy.LocPLproduces more accurate and biologically meaningful reconstructions on a versatile set of signaling pathways.LocPLis a powerful tool to automatically reconstruct signaling pathways from PPIs that leverages cellular localization information about proteins. The underlying dynamic program and signaling model are flexible enough to study cellular signaling under different settings of signaling flow across the cellular compartments.

Keywords

FOS: Computer and information sciences, Cell signaling, Artificial intelligence, Signaling pathways, Interactome, Protein-Protein Interaction Networks, Signal transduction, Gene, Computational biology, Automation, Protein-protein interaction, Protein Interaction Mapping, Biology (General), Biological pathway, Biological networks, Physics, Life Sciences, Focus (optics), Analysis of Gene Interaction Networks, Programming language, Stochasticity in Gene Regulatory Networks, Protein Transport, Medicine, Algorithms, Protein Binding, Signal Transduction, Cell biology, QH301-705.5, Bioinformatics, Computer applications to medicine. Medical informatics, R858-859.7, Pathway Analysis, Set (abstract data type), Biochemistry, Genetics and Molecular Biology, Health Sciences, Genetics, Humans, Molecular Biology, Biology, Pharmacology, Signaling proteins, Protein Structure Prediction and Analysis, Protein localization, Research, Metabolic Engineering and Synthetic Biology, Computational Biology, Proteins, Natural Products as Sources of New Drugs, Optics, Computer science, Biological Network Integration, FOS: Biological sciences, Gene expression

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
4
Average
Average
Average
Green
gold