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Team:ETHZ Basel/Modeling
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= Mathematical Modeling Overview = | = Mathematical Modeling Overview = | ||
| - | [[Image:ETHZ_Basel_molecular_comb.png|thumb|400px|'''Schematical overview of the devices and change upon light pulse induction.''' LSP refers to light switch protein, AP to anchor protein, anchor to the plasmid anchor and Che to the attacked protein of the chemotaxis pathway.]] | + | [[Image:ETHZ_Basel_molecular_comb.png|thumb|400px|'''Schematical overview of the devices and change upon light pulse induction.''' LSP refers to light switch protein, AP to anchor protein, anchor to the plasmid anchor and Che to the attacked protein of the chemotaxis pathway. The core component of E. lemming is the fusion of one light-sensitive protein (LSP1) to a protein of the chemotaxis pathway (Che). Upon change of wavelength of light pulses, this component will dimerize with the corresponding light-sensitive protein (LSP2), which is linked to an anchor protein, bound to an anchor (plasmid). The result is a change of the spatial localization of Che and perturbation of the chemotaxis pathway, which ultimately leads to a different tumbling/directed movement state ratio. |
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| - | In order to support [[Team:ETHZ_Basel/Biology|wet laboratory experiments]] and to create a test bench for the [[Team:ETHZ_Basel/InformationProcessing|information processing]] part, a | + | In order to support [[Team:ETHZ_Basel/Biology|wet laboratory experiments]] and to create a test bench for the [[Team:ETHZ_Basel/InformationProcessing|information processing]] part, a mathematical model of E. lemming was created. This goal was achieved by implementing and combining deterministic molecular models of the individual parts and probabilistic model for the bacterial movement. |
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== Implementation of mathematical models == | == Implementation of mathematical models == | ||
| - | === Individual molecular models === | + | === Individual molecular and mathematical models === |
| - | In a first step, we implemented individual molecular models of subdevices. | + | In a first step, we implemented individual molecular models of the subdevices and a mathematical model of the bacterial movement. |
* [[Team:ETHZ_Basel/Modeling/Light_Switch|'''Light Switch''']]: based upon the light-sensitive dimerizing Arabidopsis proteins PhyB and PIF3. | * [[Team:ETHZ_Basel/Modeling/Light_Switch|'''Light Switch''']]: based upon the light-sensitive dimerizing Arabidopsis proteins PhyB and PIF3. | ||
* [[Team:ETHZ_Basel/Modeling/Chemotaxis|'''Chemotaxis''']]: two similar models of the chemotactic receptor pathway. | * [[Team:ETHZ_Basel/Modeling/Chemotaxis|'''Chemotaxis''']]: two similar models of the chemotactic receptor pathway. | ||
| - | * [[Team:ETHZ_Basel/Modeling/Movement|'''Movement''']]: a probabilistic model of E. coli movement, determined by distribution of input bias. | + | * [[Team:ETHZ_Basel/Modeling/Movement|'''Bacterial Movement''']]: a probabilistic model of E. coli movement, determined by distribution of input bias. |
| - | === Combined molecular models === | + | === Combined molecular and mathematical models === |
[[Image:ETHZ_Basel_models_overview_comb.png|thumb|400px|'''Combined models.''' Coupled individual models for the simulation of the whole process and their interfaces.]] | [[Image:ETHZ_Basel_models_overview_comb.png|thumb|400px|'''Combined models.''' Coupled individual models for the simulation of the whole process and their interfaces.]] | ||
The next step, combination of the individual molecular models to a comprehensive model of E. lemming was achieved in two substeps: | The next step, combination of the individual molecular models to a comprehensive model of E. lemming was achieved in two substeps: | ||
Revision as of 11:52, 19 October 2010
Mathematical Modeling Overview
In order to support wet laboratory experiments and to create a test bench for the information processing part, a mathematical model of E. lemming was created. This goal was achieved by implementing and combining deterministic molecular models of the individual parts and probabilistic model for the bacterial movement.
Implementation of mathematical models
Individual molecular and mathematical models
In a first step, we implemented individual molecular models of the subdevices and a mathematical model of the bacterial movement.
- Light Switch: based upon the light-sensitive dimerizing Arabidopsis proteins PhyB and PIF3.
- Chemotaxis: two similar models of the chemotactic receptor pathway.
- Bacterial Movement: a probabilistic model of E. coli movement, determined by distribution of input bias.
Combined molecular and mathematical models
The next step, combination of the individual molecular models to a comprehensive model of E. lemming was achieved in two substeps:
- Light switch - Chemotaxis: used to provide support for wet laboratory.
- Chemotaxis - Movement: complete mathematical model.
Interworking: From mathematical modeling to biology and back
Insights for wet laboratory
To create the biological implementation of E. lemming, the parts of the core components had to be chosen in an order to improve chances to result in a functioning ensemble. By using the combined molecular models for in silico evaluation of the best possible parts, it was possible to reduce the amount of different combinations to be tested.
Wet laboratory evaluation results have showed, that molecular modeling and experimental biology can collaborate to gain new insight for both perceptions of the problem.
Insights for information processing
In order to adjust the controller to have optimal light pulse rates, the combined molecular model has been used to determine the corresponding time constants.
Information processing evaluation results provide further information how this has been accomplished.
Test bench for information processing
In order to create a first test bench for the information processing pipeline, the combined molecular models have been used to create and evaluate the controller. By providing an input port for light pulse and an output port for movement, it was possible to close the loop and simulate the whole system.
