Tokyo/Works

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(4.<span style="color:#ff33cc;">Wet </span>:  Assay2 on "Cell-produced" AHL and Expression comparison)
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このように、ある遺伝子回路をシミュレーションを行いながらつくっていくと交換というこ必要性が増してくると思われる。そこで、我々は交換のために有用な手段を提案する。(⇒アダプター)-->
このように、ある遺伝子回路をシミュレーションを行いながらつくっていくと交換というこ必要性が増してくると思われる。そこで、我々は交換のために有用な手段を提案する。(⇒アダプター)-->
Through the experiments mentioned above, we have found that our model can be completed by changing some of the parts employed so far. Continuing such simulation oriented construction of genetic circuit, it will be increasingly necessary to exchange parts. Here we would like to offer useful means for part exchanges.  
Through the experiments mentioned above, we have found that our model can be completed by changing some of the parts employed so far. Continuing such simulation oriented construction of genetic circuit, it will be increasingly necessary to exchange parts. Here we would like to offer useful means for part exchanges.  
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<br><br>'''Based on the results from wet experiments, the next dry approach - analysis and simulation - should be performed, which will in turn be testified and confirmed by wet experiments. Continueing these processes, if time permits, would further sophisticate and complete our model.'''([[Tokyo/Works/Future works |See more.]])
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<br><br>'''Based on the results from wet experiments, the next dry approach - analysis and simulation - should be performed, which will in turn be testified and confirmed by wet experiments. Continueing these processes, if time permits, would further sophisticate and complete our model. '''([[Tokyo/Works/Future works |See more.]])

Revision as of 12:12, 25 October 2007


Abstract  Concept & Model  Requirements  Genetic_circuit  Works  About_our_team

  0. Hybrid promoter  1. Formulation  2. Assay1  3. Simulation  4. Assay2  5. Future works

以下Worksのアブストとなる文章に。上下との話のつながりも明記。

How to reach our goal

We have alternatly implemented Wet and Dry experiments to achieve our goal

Our purpose is the construction and development of genetic circuit to establish "coexistence stability" model. We have alternately employed Dry and Wet approaches. We have drew a navigational chart on our project, which has been confirmed and reinforced by the data from Wet approaches.

0. Wet : Hybrid promoter

First, the newly devised promoter sensed the Two inputs is necessary for the Genetic_circuit.

We have created a new hybrid promoter and did its functional check. This newly devised hybrid promoter regulated by two inputs is essential to the genetic circuit in our project. Since there are no parts available that meet required conditions - activated by AHL and repressed by LacI - among previous publishments as well as BioBrick parts, we started with the design of its sequence.  (See more.)
Hybridgraph.JPGHybridpromoter.JPG

1.Dry :  Formulation

Second, we tired to mathmatically express our model.
From simple equations, the equations necessary for our model have been deviated step by step. In the final step a stochastic differential equation is used.(See more.)
Expression4-1.jpg

2.Wet :  Assay1 using "Externally added" materials

To determine the parameter of Hill coefficients, promoter assays were conducted. (See more.)
Hill AHL.JPG|Hill IPTG.JPG

3.Dry :  Simulation

Using the data from actual experiments, we simulated behaviors of our model.
Based on stochastic simulation using parameters obtained from our wet experiments, we have confirmed that the whole system becomes unstable when there are only idlers left, and then, they become either of workers and idlers. Also we have determined other parameters necessary for the desired behavior of this system. (See more.)



Tokyo simulation s2.jpg

4.Wet :  Assay2 on "Cell-produced" AHL and Expression comparison

Here the simulation results were tested by actual wet experiments.
Whether the parameters obtained in 3 is feasible in actual Wet experiments was tested by focusing on the amount of cell-produced AHL as well as the strength of the promoters. Indication from the result is applied for the next work.(See more.)

5.Future works

Through the experiments mentioned above, we have found that our model can be completed by changing some of the parts employed so far. Continuing such simulation oriented construction of genetic circuit, it will be increasingly necessary to exchange parts. Here we would like to offer useful means for part exchanges.

Based on the results from wet experiments, the next dry approach - analysis and simulation - should be performed, which will in turn be testified and confirmed by wet experiments. Continueing these processes, if time permits, would further sophisticate and complete our model. (See more.)