Title:
Computational modeling of a metabolic pathway in ceramide de novo synthesis

dc.contributor.author Dhingra, Shobhika en_US
dc.contributor.author Freedenberg, Melissa en_US
dc.contributor.author Quo, Chang Feng en_US
dc.contributor.author Merrill, Alfred H. en_US
dc.contributor.author Wang, May Dongmei en_US
dc.contributor.corporatename Georgia Institute of Technology. Dept. of Biomedical Engineering en_US
dc.contributor.corporatename Emory University. Dept. of Biomedical Engineering en_US
dc.contributor.corporatename Georgia Institute of Technology. School of Biology en_US
dc.date.accessioned 2012-01-06T19:40:58Z
dc.date.available 2012-01-06T19:40:58Z
dc.date.issued 2007-08
dc.description ©2007 IEEE. Personal use of this material is permitted. Permission from IEEE must be obtained for all other users, including reprinting/ republishing this material for advertising or promotional purposes, creating new collective works for resale or redistribution to servers or lists, or reuse of any copyrighted components of this work in other works en_US
dc.description DOI: 10.1109/IEMBS.2007.4352561
dc.description Presented at the 29th Annual International Conference of the IEEE EMBS, Cité Internationale, Lyon, France , August 23-26, 2007.
dc.description.abstract Studies have implicated ceramide as a key molecular agent in regulating programmed cell death, or apoptosis. Consequently, there is significant potential in targeting intracellular ceramide as a cancer therapeutic agent. The cell’s major ceramide source is the ceramide de novo synthesis pathway, which consists of a complex network of interdependent enzyme-catalyzed biochemical reactions. To understand how ceramide works, we have initiated the study of the ceramide de novo synthesis pathway using computational modeling based on fundamental principles of biochemical kinetics. Specifically, we designed and developed the model in MATLAB SIMULINK for the behavior of dihydroceramide desaturase. Dihydroceramide desaturase is one of three key enzymes in the ceramide de novo synthesis pathway, and it converts a relatively inert precursor molecule, dihydroceramide into biochemically reactive ceramide. A major issue in modeling is parameter estimation. We solved this problem by adopting a heuristic strategy based on a priori knowledge from literature and experimental data. We evaluated model accuracy by comparing the model prediction results with interpolated experimental data. Our future work includes more experimental validation of the model, dynamic rate constants assessment, and expansion of the model to include additional enzymes in the ceramide de novo synthesis pathway. en
dc.identifier.citation Dhingra, S.; Freedenberg, M.; Quo, C.F.; Merrill, A.H.; Wang, M.D., "Computational Modeling of A Metabolic Pathway in Ceramide de novo Synthesis," Engineering in Medicine and Biology Society, 2007. EMBS 2007. 29th Annual International Conference of the IEEE , 2007, 1405-1408. en_US
dc.identifier.doi 10.1109/IEMBS.2007.4352561
dc.identifier.isbn 978-1-4244-0787-3
dc.identifier.issn 1557-170X
dc.identifier.uri http://hdl.handle.net/1853/42166
dc.language.iso en_US en
dc.publisher Georgia Institute of Technology en
dc.publisher.original Institute of Electrical and Electronics Engineers
dc.subject Computational modeling en
dc.subject De novo synthesis en
dc.subject Dihydroceramide desaturase en
dc.subject Enzyme-catalyzed biochemical reaction en
dc.subject Enzymes en
dc.subject Metabolic pathway en
dc.subject Molecular agent en
dc.subject Programmed cell death regulation en
dc.title Computational modeling of a metabolic pathway in ceramide de novo synthesis en
dc.type Text
dc.type.genre Proceedings
dspace.entity.type Publication
local.contributor.author Merrill, Alfred H.
local.contributor.author Wang, May Dongmei
local.contributor.corporatename College of Sciences
local.contributor.corporatename School of Biological Sciences
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