Team:ETH Zurich/Achievements
From 2011.igem.org
(Difference between revisions)
(→Modeling) |
|||
Line 9: | Line 9: | ||
=Modeling= | =Modeling= | ||
- | * We made a [[Team:ETH_Zurich/Modeling/Microfluidics|reaction-diffusion model]] for the toxic molecule gradient formation in a channel and got a feeling about the feasibility of our ideas and channel dimensions. | + | * We made a [[Team:ETH_Zurich/Modeling/Microfluidics|'''reaction-diffusion model''']] for the toxic molecule gradient formation in a channel and got a feeling about the feasibility of our ideas and channel dimensions. |
- | * We approximated the gradient analytically and checked that it almost coincides with the numerically obtained one. | + | * We approximated the '''gradient analytically''' and checked that it almost coincides with the '''numerically''' obtained one. |
- | * We made a [[Team:ETH_Zurich/Modeling/SingleCell|single cell model]] describing our circuit and verified its operation. | + | * We made a [[Team:ETH_Zurich/Modeling/SingleCell|'''single cell model''']] describing our circuit and verified its operation. |
- | * We performed a [[Team:ETH_Zurich/Modeling/Analysis|robustness analysis]] of our system to see how the band behaves upon parameter variations and concluded that it is robust and monostable. | + | * We performed a [[Team:ETH_Zurich/Modeling/Analysis|'''robustness analysis''']] of our system to see how the band behaves upon parameter variations and concluded that it is robust and monostable. |
- | * We performed [[Team:ETH_Zurich/Modeling/Stochastic|stochastic analysis]] to see how the GFP band reacts upon noise and confirmed one more time its robustness | + | * We performed [[Team:ETH_Zurich/Modeling/Stochastic|'''stochastic analysis''']] to see how the GFP band reacts upon noise and confirmed one more time its robustness |
- | * We integrated the single cell model and the reaction-diffusion model in a [[Team:ETH_Zurich/Modeling/Combined|combined 3D spatiotemporal reaction-diffusion model]], simulated for various channel dimensions to get a feeling how the GFP band will move and how the alarm is activated | + | * We integrated the single cell model and the reaction-diffusion model in a [[Team:ETH_Zurich/Modeling/Combined|'''combined 3D spatiotemporal reaction-diffusion model''']], simulated for various channel dimensions to get a feeling how the GFP band will move and how the alarm is activated |
* We extracted some information about the channel dimensions from the model and [[Team:ETH Zurich/Process/Microfluidics|used this information in the actual channel design]]. | * We extracted some information about the channel dimensions from the model and [[Team:ETH Zurich/Process/Microfluidics|used this information in the actual channel design]]. | ||
{{:Team:ETH Zurich/Templates/SectionEnd}} | {{:Team:ETH Zurich/Templates/SectionEnd}} |
Revision as of 15:15, 28 October 2011
SmoColi - Achievements
Modeling
- We made a reaction-diffusion model for the toxic molecule gradient formation in a channel and got a feeling about the feasibility of our ideas and channel dimensions.
- We approximated the gradient analytically and checked that it almost coincides with the numerically obtained one.
- We made a single cell model describing our circuit and verified its operation.
- We performed a robustness analysis of our system to see how the band behaves upon parameter variations and concluded that it is robust and monostable.
- We performed stochastic analysis to see how the GFP band reacts upon noise and confirmed one more time its robustness
- We integrated the single cell model and the reaction-diffusion model in a combined 3D spatiotemporal reaction-diffusion model, simulated for various channel dimensions to get a feeling how the GFP band will move and how the alarm is activated
- We extracted some information about the channel dimensions from the model and used this information in the actual channel design.
Biology
- We improved the pSB6A1 Plasmid to standard 5: [http://partsregistry.org/Part:BBa_K625005 pSB6A5]
- We created the [http://partsregistry.org/Part:BBa_K625000 BioBrick LacIM1] which is a codon modified LacI for multiplasmid operations
- We created two improved version of the PU BioBrick
- We successfully tested the channel in terms of cell viability and GFP synthesis
- We could established a gradient of a small molecule (IPTG and arabinose) in a tube and also in the microfluidic channel
Microfluidics
- We sistematically came up with the current channel design through a process of developing and refining chain of ideas for different designs.
- Modeling help to improved the channel design
- We participated in the PDMS channel construction.
Human Practices
- We presented Synthetic Biology and iGEM to our fellow students in the CBB get together afternoon.
- We presented iGEM and our project to the general public on the BSSE Open House Day through a poster and a slide show.
- We also made a survey with critical questions related to Synthetic Biology and iGEM, asked people to fill it out and analyzed the results.
- ETH GLOBE and NZZ (Neue Zeitung Zürich) will write about our participation at iGEM World Championship Jamboree
- We helped the Edinburgh 2011 iGEM team with debugging their MATLAB cellulase model.
Personal achievements
- xx managed to move the Dropbox folder to another location, thus making it look empty for the others.
- xx accidentally modified an other teams wiki for 1 min
- xx and xy slept the whole boat trip in Amsterdam
- xy found a mistake in the PowerPoint in the morning before the presentation ("And the channel turns read")
- xy managed to sleep at two chairs in the lab
- We had fun!