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dc.contributor.authorKöksal, Ali Sinan
dc.contributor.authorBeck, Kirsten
dc.contributor.authorCronin, Dylan R.
dc.contributor.authorCamp, Nathan D.
dc.contributor.authorMacGilvray, Matthew E.
dc.contributor.authorBodík, Rastislav
dc.contributor.authorFisher, Jasmin
dc.contributor.authorMcKenna, Aaron
dc.contributor.authorSrivastava, Saurabh
dc.contributor.authorWolf Yadlin, Alejandro Marcelo
dc.contributor.authorFraenkel, Ernest
dc.contributor.authorGitter, Anthony
dc.date.accessioned2018-10-22T18:08:46Z
dc.date.available2018-10-22T18:08:46Z
dc.date.issued2018-09
dc.identifier.issn22111247
dc.identifier.urihttp://hdl.handle.net/1721.1/118655
dc.description.abstractWe present a method for automatically discovering signaling pathways from time-resolved phosphoproteomic data. The Temporal Pathway Synthesizer (TPS) algorithm uses constraint-solving techniques first developed in the context of formal verification to explore paths in an interaction network. It systematically eliminates all candidate structures for a signaling pathway where a protein is activated or inactivated before its upstream regulators. The algorithm can model more than one hundred thousand dynamic phosphosites and can discover pathway members that are not differentially phosphorylated. By analyzing temporal data, TPS defines signaling cascades without needing to experimentally perturb individual proteins. It recovers known pathways and proposes pathway connections when applied to the human epidermal growth factor and yeast osmotic stress responses. Independent kinase mutant studies validate predicted substrates in the TPS osmotic stress pathway. Köksal et al. present a computational technique, the temporal pathway synthesizer (TPS), that combines time series global phosphoproteomic data and protein-protein interaction networks to reconstruct the vast signaling pathways that control post-translational modifications.en_US
dc.description.sponsorshipNational Science Foundation (U.S.) ( grant DBI-1553206)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (training grant T32-HL007312)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant U01-CA184898)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant U54-NS09104)en_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.celrep.2018.08.085en_US
dc.rightsCreative Commons Attribution 4.0 International Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceElsevieren_US
dc.titleSynthesizing Signaling Pathways from Temporal Phosphoproteomic Dataen_US
dc.typeArticleen_US
dc.identifier.citationKöksal, Ali Sinan, Kirsten Beck, Dylan R. Cronin, Aaron McKenna, Nathan D. Camp, Saurabh Srivastava, Matthew E. MacGilvray, et al. “Synthesizing Signaling Pathways from Temporal Phosphoproteomic Data.” Cell Reports 24, no. 13 (September 2018): 3607–3618.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratoryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.mitauthorMcKenna, Aaron
dc.contributor.mitauthorSrivastava, Saurabh
dc.contributor.mitauthorWolf Yadlin, Alejandro Marcelo
dc.contributor.mitauthorFraenkel, Ernest
dc.contributor.mitauthorGitter, Anthony
dc.relation.journalCell Reportsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-10-22T17:07:41Z
dspace.orderedauthorsKöksal, Ali Sinan; Beck, Kirsten; Cronin, Dylan R.; McKenna, Aaron; Camp, Nathan D.; Srivastava, Saurabh; MacGilvray, Matthew E.; Bodík, Rastislav; Wolf-Yadlin, Alejandro; Fraenkel, Ernest; Fisher, Jasmin; Gitter, Anthonyen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9249-8181
dc.identifier.orcidhttps://orcid.org/0000-0002-5324-9833
mit.licensePUBLISHER_CCen_US


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