Abstract
In modeling whole cells we try to understand complex properties of cells by combining interlocking transport and regulatory mechanisms. We use a modular approach and develop models of each individual process separately using available experimental data. We then construct progressively more complete models by combining components to understand how they work together. Sometimes, we proceed in the opposite order, beginning with a comprehensive model, which we simplify in order to determine the minimal essential elements. One particularly useful simplification technique is to exploit separation of time scales to set fast processes to equilibrium as described in Chapter 4.
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Suggestions for Further Reading
Ryanodine receptor adaptation and Ca2+-induced Ca2+ release-dependent Ca2+ oscillations, Joel Keizer and Leslie Levine. This paper is the original source for the Keizer-Levine model (Keizer and Levine 1996).
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Contributions of modeling to understanding stimulus-secretion coupling in pancreatic β-cells, Arthur Sherman. A review of β-cell modeling oriented toward biologists (Sherman 1996).
Calcium and membrane potential oscillations in pancreatic β-cells, Arthur Sherman. A mathematical tutorial centered on β-cell models with some connections to general modeling of bursting. Covers phase plane and bifurcation analysis (Sherman 1997).
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© 2002 Springer-Verlag New York, Inc.
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Sherman, A.S., Li, YX., Keizer, J.E. (2002). Whole—Cell Models. In: Fall, C.P., Marland, E.S., Wagner, J.M., Tyson, J.J. (eds) Computational Cell Biology. Interdisciplinary Applied Mathematics, vol 20. Springer, New York, NY. https://doi.org/10.1007/978-0-387-22459-6_5
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DOI: https://doi.org/10.1007/978-0-387-22459-6_5
Publisher Name: Springer, New York, NY
Print ISBN: 978-0-387-95369-4
Online ISBN: 978-0-387-22459-6
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