Latest revision as of 16:50, 27 October 2010

Combined Models

Combined model. Coupled individual models for the simulation of the entire process and their interfaces. The concentration of CheYp determines the movement bias.

Interface

To create the complete model of E. lemming, the individual modules chemotaxis pathway, light switch and movement model were coupled, by defining input - output interfaces. The combination was achieved in two steps:

First, the deterministic light switch and chemotaxis models were combined corresponding to the different devices: PhyB/PIF3 light switch and ALR light switch.
Second, the stochastic movement model was combined with the light switch - chemotaxis model. The interface was defined as the dependency CheYp - directed movement probability (or the bias). At every time point of the simulation, the next state (directed movement/tumbling) of the bacterium was selected, based on the value of the input bias.

PhyB/PIF3 light switch - Chemotaxis

Schematical overview of the chemotaxis pathway. MCPs refers to the membrane receptor proteins and Che to the intracellular chemotaxis proteins.

The following assumptions have been made according to the molecular mechanism to link the light switch and chemotaxis models: Upon red light pulse induction, the two light-sensitive proteins dimerize and thus the coupled Che protein is spatially dislocated. This means

CheR is not able to methylate the MCPs anymore,
CheY can't be phosphorylated and interact with the motor anymore; nevertheless, it still can be dephosphorylated.
Since CheB and CheZ regulate the chemotactic receptor pathway inverse compared to CheR and CheY, they repress tumbling
CheB is not able to demethylate the MCPs and can't be phosphorylated anymore, but still can be dephosphorylated,
CheZ can't dephosphorylate CheY anymore (This assumption is very unsteady, since CheY is not strictly located).

All of these assumptions will lead to a decrease of tumbling / directed movement ratio upon red light induction and an increase of corresponding far-red light induction.

Archeal light receptor - Chemotaxis

Schematical overview of the chimeric chemotaxis pathway. ALR refers to the archeal light receptor, MCPs to the membrane receptor proteins and Che to the intracellular chemotaxis proteins.

We replaced the usual chemo receptor in E. coli with a receptor that receives light and gives rise to the same down stream activity of the chemotaxis path way, thus giving birth to the E. lemming - the E. coli that can be controlled by light inputs.

This idea was modeled & simulated as described in Archeal light receptor. Then it was successfully implemented in the laboratory. Click here to see the E. lemming in action, at ETH Zurich!

Chemotaxis - Movement

The combination of the deterministic and probabilistic models was (first) the biggest challenge and (afterwards) the biggest accomplishment in combining the models. Besides its theoretical complexity, the complete coupling is also conceptually very important. It closes the loop of our E. lemming modeling and it combines two different types of models: deterministic and stochastic, under the same global approach. The two models have different timesteps, the molecular one being much faster than the stochastic one, therefore their combination has been done via Simulink interface. Both models have been independently numerically integrated and the output of the deterministic model was passed as an input to the stochastic one, at every slower time-step. The main assumption we used in the complete coupling was that the mean run length is a function of the bias, while mean tumbling length is bias - independent.

Download

The combined model is included within the Matlab Toolbox and can be downloaded there.

@@ Line 5: / Line 5: @@
 [[Image:ETHZ_Basel_molecular.png|thumb|400px|'''Combined model.''' Coupled individual models for the simulation of the entire process and their interfaces. The concentration of CheYp determines the movement bias.]]
-To create the complete model of E. lemming, the individual modules [[Team:ETHZ_Basel/Modeling/Chemotaxis| chemotaxis pathway]], [[Team:ETHZ_Basel/Modeling/Light_switch| light switch]] and [[Team:ETHZ_Basel/Modeling/Movement| movement model]] were coupled, by defining input - output interfaces. The combination was achieved in two steps:
+== Interface ==
+To create the complete model of E. lemming, the individual modules chemotaxis pathway, light switch and movement model were coupled, by defining input - output interfaces. The combination was achieved in two steps:
-* First, the deterministic light switch and chemotaxis models were combined by two different ways: The archeal light receptor is linked to the chemotaxis model by replacing the aspartate input. The PhyB/PIF3 is linked by the common LSP1-Che species.
+*First, the deterministic light switch and chemotaxis models were combined corresponding to the different devices: PhyB/PIF3 light switch and ALR light switch.
+*Second, the stochastic movement model was combined with the light switch - chemotaxis model. The interface was defined as the dependency CheYp - directed movement probability (or the bias). At every time point of the simulation, the next state (directed movement/tumbling) of the bacterium was selected, based on the value of the input bias.
-* Second, the stochastic movement model was combined with the light switch - chemotaxis model. The interface was defined as the dependency CheYp - directed movement probability (or the bias). At every time point of the simulation, the next state (directed movement/tumbling) of the bacterium was selected, based on the value of the input bias.
+== PhyB/PIF3 light switch - Chemotaxis ==
+[[Image:ETHZ_Basel_chemotactical_network.png|thumb|400px|'''Schematical overview of the chemotaxis pathway.''' MCPs refers to the membrane receptor proteins and Che to the intracellular chemotaxis proteins.]]
-== PhyB/PIF3 light switch - Chemotaxis - Movement ==
+The following assumptions have been made according to the molecular mechanism to link the light switch and chemotaxis models:
-[[Image:ETHZ_Basel_chemotactical_network.png|thumb|400px|'''Schematical overview on the chemotaxis pathway.''' MCPs refers to the membrane receptor proteins and Che are the intracellular proteins of the chemotaxis pathway.]]
+Upon red light pulse induction, the two light-sensitive proteins dimerize and thus the coupled Che protein is spatially dislocated. This means
+*CheR is not able to methylate the MCPs anymore,
+*CheY can't be phosphorylated and interact with the motor anymore; nevertheless, it still can be dephosphorylated.
+*Since CheB and CheZ regulate the chemotactic receptor pathway inverse compared to CheR and CheY, they repress tumbling
+*CheB is not able to demethylate the MCPs and can't be phosphorylated anymore, but still can be dephosphorylated,
+*CheZ can't dephosphorylate CheY anymore (This assumption is very unsteady, since CheY is not strictly located).
+All of these assumptions will lead to a decrease of tumbling / directed movement ratio upon red light induction and an increase of corresponding far-red light induction.
-* First, the deterministic light switch and chemotaxis models were combined by assuming a complete removal of a selected Che protein species by the light switch. The interface was defined as the concentration ([LSP1-Che]) of this linked device.
+== Archeal light receptor - Chemotaxis ==
+[[Image:ETHZ_Basel_archean_chemotactical_network.png|thumb|400px|'''Schematical overview of the chimeric chemotaxis pathway. '''ALR refers to the archeal light receptor, MCPs to the membrane receptor proteins and Che to the intracellular chemotaxis proteins.]] We replaced the usual chemo receptor in E. coli with a receptor that receives light and gives rise to the same down stream activity of the chemotaxis path way, thus giving birth to the E. lemming - the E. coli that can be controlled by light inputs.
-* Second, the stochastic movement model was combined with the light switch - chemotaxis model. The interface was defined as the dependency CheYp - directed movement probability (or the bias). At every time point of the simulation, the next state (directed movement/tumbling) of the bacterium was selected, based on the value of the input bias.
+This idea was modeled & simulated as described in [[Team:ETHZ_Basel/Modeling/Light_Switch#Archeal_light_receptor|Archeal light receptor]]. Then it was [[Team:ETHZ_Basel/Biology|successfully implemented in the laboratory]]. [[Team:ETHZ_Basel/Achievements/E_lemming|Click here]] to see the E. lemming in action, at ETH Zurich!
+== Chemotaxis - Movement ==
 The combination of the deterministic and probabilistic models was (first) the biggest challenge and (afterwards) the biggest accomplishment in combining the models. Besides its theoretical complexity, the complete coupling is also conceptually very important. It closes the loop of our E. lemming modeling and it combines two different types of models: deterministic and stochastic, under the same global approach.
+The two models have different timesteps, the molecular one being much faster than the stochastic one, therefore their combination has been done via Simulink interface. Both models have been independently numerically integrated and the output of the deterministic model was passed as an input to the stochastic one, at every slower time-step.
-The two models have different timesteps, the molecular one being much faster than the stochastic one, therefore their combination has been done via Simulink interface. Both models have been independently numerically integrated and the output of the deterministic model was passed as an input to the stochastic one, at every slower time-step.
-The main assumption we used in the complete coupling was that the mean run length is a function of the bias, while mean tumbling length is bias - independent.
-[[Image:ETHZ_Basel_models_overview_comb.png|thumb|left|400px|'''Combined model.''' Coupled individual models for the simulation of the entire process and their interfaces.]]
-<br clear="all" />
-== Archeal light switch - Chemotaxis ==
-[[Image:ETHZ_Basel_archean_chemotactical_network.png|thumb|400px|'''Schematical overview of the chimeric chemotaxis pathway. '''ALR refers to the archeal light receptor, MCPs to the membrane receptor proteins and Che to the intracellular chemotaxis proteins.]]
-== Chemotaxis - Movement ==
-The combination of the deterministic and probabilistic models was (first) the biggest challenge and (afterwards) the biggest accomplishment in combining the models. Besides its theoretical complexity, the complete coupling is also conceptually very important. It closes the loop of our E. lemming modeling and it combines two different types of models: deterministic and stochastic, under the same global approach.
-The two models have different timesteps, the molecular one being much faster than the stochastic one, therefore their combination has been done via Simulink interface. Both models have been independently numerically integrated and the output of the deterministic model was passed as an input to the stochastic one, at every slower time-step.
 The main assumption we used in the complete coupling was that the mean run length is a function of the bias, while mean tumbling length is bias - independent.
 == Download ==
 The combined model is included within the [[Team:ETHZ_Basel/Achievements/Matlab_Toolbox|Matlab Toolbox]] and can be downloaded there.

Team:ETHZ Basel/Modeling/Combined

From 2010.igem.org