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Team:KULeuven/Model/Overview
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==== Position in the system ==== | ==== Position in the system ==== | ||
| - | For each of the subsystems (compartments) we started with the idea of what it was supposed to do, considering it as a black-box system (as described in the [https://2008.igem.org/Team:KULeuven/Project project page]). . | + | For each of the subsystems (compartments) we started with the idea of what it was supposed to do, considering it as a black-box system (as described in the [https://2008.igem.org/Team:KULeuven/Project project page]). To make sure that Dr. Coli was able to do his work properly, we had to design several subsystems and be well aware of the different interfaces between these subsystems. |
==== Describing the system ==== | ==== Describing the system ==== | ||
Revision as of 21:34, 17 August 2008
Introduction
As an introduction to modeling we've made a small presentation for the workout sessions of the first meeting. This presentation handles the following items:
- some definitions
- the difference between white box and black box models with an example
- focus on the role of ODE's
- the need for modeling
- some modeling tools
- and iGEM modeling
This presentation is mainly based on the wiki of ETH Zürich 2006/2007.
Why modeling?
Modeling steps
Position in the system
For each of the subsystems (compartments) we started with the idea of what it was supposed to do, considering it as a black-box system (as described in the project page). To make sure that Dr. Coli was able to do his work properly, we had to design several subsystems and be well aware of the different interfaces between these subsystems.
Describing the system
We first searched for existing components which could be able to perform the requested task ... (todo: ODE/parameters)
Models
We implemented these subsystems in both [http://www.systems-biology.org/cd/ Celldesigner] and the [http://www.mathworks.com/access/helpdesk/help/toolbox/simbio/ MATLAB Symbiology Toolbox]. A nice tutorial for modeling in Celldesigner can be found on [http://openwetware.org/wiki/Imperial_College/Courses/Spring2008/Synthetic_Biology/Computer_Modelling_Practicals Imperial College Computer Modelling Practicals Spring 2008]. These 2 environments offer a grapical user-interface which makes it easy to implement biochemical pathways (and the kinetic laws which govern these). In the pictures in each of the subsytems you can see clearly the influence of the different species: activation, repression, complexation, ... We also provide links to the actual implemented diagrams which can be freely downloaded to simulate the subsystems yourself.
Simulation(s)
...
Sensitivity Analysis
Good modeling practice requires that the modeler provides an evaluation of the confidence in the model, possibly assessing the uncertainties associated with the modeling process and with the outcome of the model itself. Uncertainty and Sensitivity Analysis offer valid tools for characterizing the uncertainty associated with a model. Uncertainty analysis (UA) quantifies the uncertainty in the outcome of a model. Sensitivity Analysis has the complementary role of ordering by importance the strength and relevance of the inputs in determining the variation in the output. Sensitivity analysis lets you calculate the time-dependent sensitivities of all the species states with respect to species initial conditions and parameter values in the model.
A sensitivity analysis is needed e.g. when some of the parameter values are not known. The true value of a parameter is unimportant when the most essential species states are insensitive to the unknown parameter. Only for the sensitive unknown parameters are experiments needed to determine their true values. In our project we have been able to find hypothetical values for all used parameters, but a sensitivity analyses is nevertheless always valuable to detect critical parameters. These are the parameter values on which our project critically depends and which should be analyzed/characterized as exact as possible.
todo: add (search?) formula with which these anaylises are performed.
Important notes
1. The idea of a pulsgenerator as reset mechanism has been cancelled for the following reasons:
- it takes too long before the proposed system generates a pulse-like event
- the pulse itself is too long
- a constant lactonase production sequence generates enough lactonase to reset the timer
More information about this problem and the solution can be found on Reset-page.
2. A mathematical analyses of the memory has been done to prove that it has 2 stable states and to describe the boundary which separates the trajectories leading to one of the steady states.
More information about this problem and the solution can be found on Memory-page.
