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Team:TUDelft/Preliminary approaches
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='''Preliminary Approaches'''= | ='''Preliminary Approaches'''= | ||
| + | ===Negative transcriptional cascade=== | ||
| - | + | Based on the work of Hooshangi S et al 2005 [[https://2009.igem.org/Team:TUDelft/Module_3_References 4]] and the project requirements, the following scheme was proposed. | |
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| - | Based on the work of Hooshangi S et al 2005 | + | |
| - | [[Image:Figure4Delay.jpg|thumb|550px|Figure 4. Genes 1 and 3 are present in the cell and they are produced all the time (black). Genes 2 and 4 (green) are in the self destructive plasmid (SDP).]] | + | [[Image:Figure4Delay.jpg|center|thumb|550px|Figure 4. Genes 1 and 3 are present in the cell and they are produced all the time (black). Genes 2 and 4 (green) are in the self destructive plasmid (SDP).]] |
| - | Protein 1 starts the circuit activating (or repressing the repressor of) the promoter of gene 2, for proof of concept gene 1 can be changed for a signal molecule. The concentration of protein 2 will increase and achieve the threshold concentration to repress gene 3. At this point the production of protein 3 stops. As the concentration of protein 3 decreases due to its degradation, the repression of gene 4 will not longer exist and the production of protein 4 (restriction enzyme or fluorescent protein) starts. In order to make a longer or shorter delay the protein production and degradation rates have to be considered. For the former, we can “play” with the ribosome binding site (RBS) and promoter strength. The degradation can be controlled by protein stability, induction of degradation and up-down regulation of degradation enzymes. | + | Protein 1 starts the circuit, activating (or repressing the repressor of) the promoter of gene 2, for proof of concept gene 1 can be changed for a signal molecule. The concentration of protein 2 will increase and achieve the threshold concentration to repress gene 3. At this point the production of protein 3 stops. As the concentration of protein 3 decreases due to its degradation, the repression of gene 4 will not longer exist and the production of protein 4 (restriction enzyme or fluorescent protein) starts. In order to make a longer or shorter delay, the protein production and degradation rates have to be considered. For the former, we can “play” with the ribosome binding site (RBS) and promoter strength. The degradation can be controlled by protein stability, induction of degradation and up-down regulation of degradation enzymes. |
| - | + | ===Positive transcriptional cascade=== | |
| - | Based on the book of Uri Alone | + | Based on the book of Uri Alone [[https://2009.igem.org/Team:TUDelft/Module_3_References 5]] and the project requirements, the next scheme was proposed. |
| - | [[Image:Figure5Delay.jpg|thumb|550px|Figure 5. Genes 1 and 3 are present in the cell and they are produced all the time (black). Genes 2 and 4 (green) are in the self destructive plasmid (SDP).]] | + | [[Image:Figure5Delay.jpg|center|thumb|550px|Figure 5. Genes 1 and 3 are present in the cell and they are produced all the time (black). Genes 2 and 4 (green) are in the self destructive plasmid (SDP).]] |
| - | Protein 1 starts the circuit activating the promoter of gene 2, for proof of concept gene 1 can be changed | + | Protein 1 starts the circuit, activating the promoter of gene 2, for the proof of concept gene 1 can be changed to a signal molecule. The concentration of protein 2 will increase and achieve the threshold concentration to induce gene 3. As the concentration of protein 3 increases, the induction of gene 4 (restriction enzyme or fluorescent protein) starts. In order to make a longer or shorter delay the protein production and degradation rates have to be considered. For the former, we can “play” with the ribosome binding site (RBS) and promoter strength. The degradation can be controlled by protein stability, induction of degradation and up-down regulation of degradation enzymes. |
[https://2009.igem.org/Team:TUDelft/Synthetic_Transcriptional_Cascade Return] | [https://2009.igem.org/Team:TUDelft/Synthetic_Transcriptional_Cascade Return] | ||
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{{Template:TUDelftiGEM2009_end}} | {{Template:TUDelftiGEM2009_end}} | ||
Latest revision as of 00:18, 22 October 2009
Preliminary Approaches
Negative transcriptional cascade
Based on the work of Hooshangi S et al 2005 [4] and the project requirements, the following scheme was proposed.
Protein 1 starts the circuit, activating (or repressing the repressor of) the promoter of gene 2, for proof of concept gene 1 can be changed for a signal molecule. The concentration of protein 2 will increase and achieve the threshold concentration to repress gene 3. At this point the production of protein 3 stops. As the concentration of protein 3 decreases due to its degradation, the repression of gene 4 will not longer exist and the production of protein 4 (restriction enzyme or fluorescent protein) starts. In order to make a longer or shorter delay, the protein production and degradation rates have to be considered. For the former, we can “play” with the ribosome binding site (RBS) and promoter strength. The degradation can be controlled by protein stability, induction of degradation and up-down regulation of degradation enzymes.
Positive transcriptional cascade
Based on the book of Uri Alone [5] and the project requirements, the next scheme was proposed.
Protein 1 starts the circuit, activating the promoter of gene 2, for the proof of concept gene 1 can be changed to a signal molecule. The concentration of protein 2 will increase and achieve the threshold concentration to induce gene 3. As the concentration of protein 3 increases, the induction of gene 4 (restriction enzyme or fluorescent protein) starts. In order to make a longer or shorter delay the protein production and degradation rates have to be considered. For the former, we can “play” with the ribosome binding site (RBS) and promoter strength. The degradation can be controlled by protein stability, induction of degradation and up-down regulation of degradation enzymes.
