E-Book, Englisch, 360 Seiten
Reihe: Chapman & Hall/CRC Mathematical & Computational Biology
Demin / Goryanin Kinetic Modelling in Systems Biology
1. Auflage 2008
ISBN: 978-1-4200-1166-1
Verlag: Taylor & Francis
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)
E-Book, Englisch, 360 Seiten
Reihe: Chapman & Hall/CRC Mathematical & Computational Biology
ISBN: 978-1-4200-1166-1
Verlag: Taylor & Francis
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)
With more and more interest in how components of biological systems interact, it is important to understand the various aspects of systems biology. Kinetic Modelling in Systems Biology focuses on one of the main pillars in the future development of systems biology. It explores both the methods and applications of kinetic modeling in this emerging field.
The book introduces the basic biological cellular network concepts in the context of cellular functioning, explains the main aspects of the Edinburgh Pathway Editor (EPE) software package, and discusses the process of constructing and verifying kinetic models. It presents the features, user interface, and examples of DBSolve as well as the principles of modeling individual enzymes and transporters. The authors describe how to construct kinetic models of intracellular systems on the basis of models of individual enzymes. They also illustrate how to apply the principles of kinetic modeling to collect all available information on the energy metabolism of whole organelles, construct a kinetic model, and predict the response of the organelle to changes in external conditions. The final chapter focuses on applications of kinetic modeling in biotechnology and biomedicine.
Encouraging readers to think about future challenges, this book will help them understand the kinetic modeling approach and how to apply it to solve real-life problems.
CD-ROM Features
Extensively used throughout the text for pathway visualization and illustration, the EPE software is available on the accompanying CD-ROM. The CD also includes pathway diagrams in several graphical formats, DBSolve installation with examples, and all models from the book with dynamic visualization of simulation results, allowing readers to perform in silico simulations and use the models as templates for further applications.
Zielgruppe
Students, researchers, and practitioners in bioinformatics and computational biology; biologists; and biophysicists.
Autoren/Hrsg.
Weitere Infos & Material
Introduction
Systems Biology, Biological Knowledge, and Kinetic Modelling
Dependence of enzyme reaction rate on the substrate concentration
What are the model limitations? Or, in other words, what can be modeled?
Cellular Networks Reconstruction and Static Modelling
Pathway reconstruction
The high-quality network reconstruction: description of the process
Visual notations: three categories
Edinburgh Pathway Editor (EPE)
Introduction
Feature summary of EPE
A flexible visual representation
Conclusion
Construction and Verification of Kinetic Models
Introduction
Basic principles of kinetic model construction
Basic principles of kinetic model verification
Study of dynamic and regulatory properties of the kinetic model
Introduction to DBSolve
Creation and analysis of the models using DBSolve: functional description
Enzyme Kinetics Modelling
Introduction
Basic principles of modeling individual enzymes and transporters
"Hyperbolic" enzymes
Allosteric enzymes
Transporters
Kinetic Models of Biochemical Pathways
Modelling of the mitochondrial Krebs cycle
Modelling of the Escherichia coli branched-chain amino acid biosynthesis
Modelling of Mitochondrial Energy Metabolism
Oxidative phosphorylation and superoxide production in mitochondria
Development of kinetic models
Description of individual processes of the model
Model predictions
Application of the Kinetic Modelling Approach to Problems in Biotechnology and Biomedicine
Study of the mechanisms of salicylate-hepatotoxic effect
Multiple target identification analysis for antituberculosis drug discovery
Application of the kinetic model of E. coli branched-chain amino acid biosynthesis to optimize production of isoleucine and valine
Conclusion and Discussion
References
Index