Difference between revisions of "Team:Czech Republic/Goals"
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* Monitored the dynamic binding of our receptors and their corresponding markers | * Monitored the dynamic binding of our receptors and their corresponding markers | ||
− | '''Module 4''' | + | '''Module 4 provided modeling and simulation support for other modules.''' |
* Developed a simulation environment CeCe to capture the complexity of cell-cell signal transmission | * Developed a simulation environment CeCe to capture the complexity of cell-cell signal transmission | ||
* Designed an IOD chemical reaction network model | * Designed an IOD chemical reaction network model | ||
Line 28: | Line 28: | ||
* Illustrated the robustness and efficiency of the IOD band design in CeCe simulations | * Illustrated the robustness and efficiency of the IOD band design in CeCe simulations | ||
− | '''Module 5''' | + | '''Module 5 allowed other modules to use microfluidics devices for their experiments.''' |
* Set of microfluidic devices fabricated by PDMS soft-lithography. | * Set of microfluidic devices fabricated by PDMS soft-lithography. | ||
* Characterization of signal transmission range between wildtype MATa and MATx Saccharomyces cerevisiae cells. | * Characterization of signal transmission range between wildtype MATa and MATx Saccharomyces cerevisiae cells. |
Revision as of 20:13, 18 September 2015
Goals
Module 1 builds synthetic haploid strains with refactored mating loci that are conjugated to make a functional IOD. These strains have the wild-type mating phenotype and differentially express a reprogrammed signalling pathway in their diploid state proving the feasibility of the clone-free assembly concept.
- Constructed a set of reporter promoters for yeast cells
- Characterized reporter promoters in all mating types
- Designed and materialized synthetic MATa and MATx strains
- Built a synthetic diploid strain with a functional yeast pheromone pathway
- Demonstrated the correct functionality of yeast pheromone pathway in synthetic diploids
Module 2 builds a set of orthogonal pheromones and receptors. These pheromone-receptor pairs enable specific localized signalling proving the feasibility of multichannel signal transmission underlying logic operations necessary for reliable diagnosis.
- Constructed a set of yeast plasmids with different mating pheromones and their receptors and contributed to the Registry with 6 BioBricks
- Verified the correct coupling of the receptors to the yeast pheromone mating pathway
- Verified the correct expression and secretion of the different pheromones
- Showed the orthogonality of the used receptors and pheromones
Module 3 builds a set of location tags that recognize common tumor surface markers and agglutinate cell populations. Location tags displayed in the correct conformation strengthen cell-cell interactions to enable localization of signal transmission.
- Expressed streptavidin, EpCAM, Anti-EpCAM scFv, c-Myc scFv and anti-HuA scFv on the surface of yeasts
- Demonstrated the ability of our receptors to bind chosen markers
- Monitored the dynamic binding of our receptors and their corresponding markers
Module 4 provided modeling and simulation support for other modules.
- Developed a simulation environment CeCe to capture the complexity of cell-cell signal transmission
- Designed an IOD chemical reaction network model
- Developed a schematic architecture for conceptual modeling of signal transmission networks
- Designed a two IOD signal transmission network suitable for the IOD band
- Illustrated the robustness and efficiency of the IOD band design in CeCe simulations
Module 5 allowed other modules to use microfluidics devices for their experiments.
- Set of microfluidic devices fabricated by PDMS soft-lithography.
- Characterization of signal transmission range between wildtype MATa and MATx Saccharomyces cerevisiae cells.
- Dynamic characterisation of signal transmission between synthetic MATa and MATx Saccharomyces cerevisiae cells.
- Comparison with mathematical model of signal transmission mechanism and estimation of the activation threshold for different cell concentrations.
- Demonstrated yeast induced blood agglutination on-chip by human antigen A displayed on cell surface by Yeast Surface Display.