Team:University of Lethbridge/Modeling

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Latest revision as of 01:00, 30 October 2008

	[http://2008.igem.org/wiki/index.php?title=Team:University_of_Lethbridge&Home ]	[http://2008.igem.org/Team:University_of_Lethbridge/Team ]	[http://2008.igem.org/Team:University_of_Lethbridge/Project ]	[http://2008.igem.org/Team:University_of_Lethbridge/Parts ]	[http://2008.igem.org/Team:University_of_Lethbridge/Modeling ]	[http://2008.igem.org/Team:University_of_Lethbridge/Notebook ]

Our Project

For our project, we decided to create a synthetic bacterium which could move towards and degrade an environmental pollutant. To direct the movement of our modified "Bacuum Cleaner," we reprogrammed the chemotaxis pathway by using a toxin-responsive riboswitch to control expression of the motility protein CheZ. CheZ catalyzes the dephosphorylation of the motility protein CheY, which promotes directed movement (chemotaxis) over the "tumbling" state of the bacterium.

We used the modeling program [http://www.pdn.cam.ac.uk/groups/comp-cell/BCT.html BCT] (Bray et al, 1993, 2007; Bray and Bourret, 1995) to verify that CheZ expression levels can be manipulated to control bacterial movement. The program [http://www.pdn.cam.ac.uk/groups/comp-cell/BCT.html BCT] simulates the chemotaxis signalling pathway in Escherichia coli and is extensively supported by [http://www.pdn.cam.ac.uk/groups/comp-cell/Mutants.html experimental data]. We used the program to demonstrate that controlling CheZ expression will control bacterial motility and to determine the amount of CheZ necessary to dephosphorylate CheY in high enough levels to produce directed movement. We modeled the E. coli strain RP437 in BCT, which is the same strain our group used as the chassis for our iGEM project.

Increasing intracellular amounts of CheZ led to increased concentration of CheY in the unphosphorylated state (Figure 1). Motility also increased, from a relative state of 0 (no movement or the tumbling state) to the relative state of 1 (continually moving in a directed manner).

Figure 1

References

Bray, D., Bourret, R. B., and Simon, M. I. 1993. Computer simulation of the phosphorylation cascade controlling bacterial chemotaxis. Mol. Biol. Cell 4, 469-482.

Bray, D., and Bourret, R. B. 1995. Computer analysis of the binding reactions leading to a transmembrane receptor-linked multiprotein complex involved in bacterial chemotaxis. Mol. Biol. Cell 6, 1367-1380.

Bray, D., Levin, M. D., and Lipkow, K. 2007. The chemotactic behavior of computer-based surrogate bacteria. Curr. Biol. 17, 12-19.

	[http://2008.igem.org/wiki/index.php?title=Team:University_of_Lethbridge&Home ]	[http://2008.igem.org/Team:University_of_Lethbridge/Team ]	[http://2008.igem.org/Team:University_of_Lethbridge/Project ]	[http://2008.igem.org/Team:University_of_Lethbridge/Parts ]	[http://2008.igem.org/Team:University_of_Lethbridge/Modeling ]	[http://2008.igem.org/Team:University_of_Lethbridge/Notebook ]

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@@ Line 36: / Line 36: @@
 For our project, we decided to create a synthetic bacterium which could move towards and degrade an environmental pollutant. To direct the movement of our modified "Bacuum Cleaner," we reprogrammed the chemotaxis pathway by using a toxin-responsive riboswitch to control expression of the motility protein CheZ. CheZ catalyzes the dephosphorylation of the motility protein CheY, which promotes directed movement (chemotaxis) over the "tumbling" state of the bacterium.
-We used the modeling program BCT (ref) to determine the level of ''CheZ'' gene expression necessary to produce dephosphorylated CheY and directed movement. Increasing intracellular concentrations of CheZ leads to increased CheY in the unphosphorylated state (Figure 1)...
+We used the modeling program [http://www.pdn.cam.ac.uk/groups/comp-cell/BCT.html <font color=yellow>BCT</font>] (Bray et al, 1993, 2007; Bray and Bourret, 1995) to verify that CheZ expression levels can be manipulated to control bacterial movement.  The program [http://www.pdn.cam.ac.uk/groups/comp-cell/BCT.html <font color=yellow>BCT</font>] simulates the chemotaxis signalling pathway in ''Escherichia coli'' and is extensively supported by [http://www.pdn.cam.ac.uk/groups/comp-cell/Mutants.html <font color=yellow>experimental data</font>]. We used the program to demonstrate that controlling CheZ expression will control bacterial motility and to determine the amount of CheZ necessary to dephosphorylate CheY in high enough levels to produce directed movement. We modeled the E. coli strain RP437 in BCT, which is the same strain our group used as the chassis for our iGEM project.
+Increasing intracellular amounts of CheZ led to increased concentration of CheY in the unphosphorylated state (Figure 1). Motility also increased, from a relative state of 0 (no movement or the tumbling state) to the relative state of 1 (continually moving in a directed manner).
 ----
-[[Image:Chez_hjfigure.jpg|400px]]
+[[Image:Chez_hj_black.gif|400px]]
 <font color=white> Figure 1
+==<span style="background-color:#000000; color:white">References</span>==
+Bray, D., Bourret, R. B., and Simon, M. I. 1993. Computer simulation of the phosphorylation cascade controlling bacterial chemotaxis. ''Mol. Biol. Cell'' 4, 469-482.
+Bray, D., and Bourret, R. B. 1995. Computer analysis of the binding reactions leading to a transmembrane receptor-linked multiprotein complex involved in bacterial chemotaxis. ''Mol. Biol. Cell'' 6, 1367-1380.
+Bray, D., Levin, M. D., and Lipkow, K. 2007. The chemotactic behavior of computer-based surrogate bacteria. ''Curr. Biol.'' 17, 12-19.
+----
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