Team:Aberdeen Scotland/parameters/invest 4

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=Relationship between K<sub>TetR</sub> and K<sub>CI</sub> when K<sub>P</sub> is 50 =
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=Relationship between K<sub>TetR</sub>, K<sub>CI</sub> and K<sub>LacI</sub> when K<sub>P</sub> is 50 =
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=Relationship between K<sub>TetR</sub> and K<sub>CI</sub> when K<sub>P</sub> is 50 and K<sub>LacI</sub> is 700 =
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We notice that K<sub>P</sub> must be around 50 molecules to let the system function. We will now explore the relationship between K<sub>TetR</sub> and K<sub>CI</sub> at the value of K<sub>P</sub>=50 molecules per cell.
We notice that K<sub>P</sub> must be around 50 molecules to let the system function. We will now explore the relationship between K<sub>TetR</sub> and K<sub>CI</sub> at the value of K<sub>P</sub>=50 molecules per cell.

Revision as of 15:08, 13 August 2009

University of Aberdeen iGEM 2009

Contents

The Input-dependent model

For this model, we no longer assume a trivial process of repression of lacI being liften and QS being turned on. The LacI repression is now a repression / induction hill function with a Kd of 1200 molecules per cell for IPGT forming IPGT lacI complexes. We assume IPGT leaks into the cell from outside. We only set the outside concentration of IPGT. For quorum sensing all we set is an elevated HSL concentration outside which is free to defuse in. We now include a feedback loop into the QS mechanism. To do this we attach a lux box onto the plasmid for producing luxR and luxI, like so:


Input Model Graph 1.jpg

However, we are taking the production strengths of this lux box to be reduced in comparison to our lux box for producing X, Y and cI. The strengths are

Production max for X, Y and cI = 0.44 pops

taken from the iGEM page of ***** and personal communication with **** on ****

Production min for X Y and cI = 0.013 pops

taken from *****

Production max for QS feedback = 0.002 pops

Production min for QS feedback = 0.00015 pops

These values are taken from the paper “ FIOADAOIDFJAOFJASDIOJASOIJADOAJSDAFOJAFOAJSD”

An important new parameter is KP. This is the dissociation constant for “P” activating the lux boxes. P is the luxR/HSL complex . To take a break from the wordy descriptions we will now show some small sections of results for this model, which should be easily interpretable after following the section about the Monte Carlo analysis

Level of KP required for system to function

here we use a Monte Carlo simulation to determine the value of KP in molecules per cell that is required for the system to function (note that the IPTG and HSL input levels added are both 10000 molecules)

Input Model Graph 10.jpg
Input Model Graph 11.jpg

Relationship between KTetR, KCI and KLacI when KP is 50

Input Model Graph 4.jpg


Relationship between KTetR and KCI when KP is 50 and KLacI is 700

We notice that KP must be around 50 molecules to let the system function. We will now explore the relationship between KTetR and KCI at the value of KP=50 molecules per cell. for this simulation we set the HSL and IPTG input levels to 50,000 molecules. In our next section we will try to calculate the minimum levels of HSL and IPTG required to activate the system correctly.


Input Model Graph 8.jpg
Input Model Graph 9.jpg

The graph shows a great deal of stochastic fluctuation, which shows this system is not very robust. Increasing KP above 50 greatly increases this problem, as does decreasing HSL outside below 50,000.

Our estimation for KTetR and KCI suggest that KTetR is less than KCI. We assume the worst case value for these two dissociation constants and set them equal to each other, at KTetR = KCI = 7000 molecules per cell.

Required input levels of IPTG and HSL

Input Model Graph 2.jpg


We start by going from 5,000 molecules to 100,000 molecules for HSL and from 10 molecules to 5,000 molecules for IPTG. we see that the sysem requires only around 2000 molecules of IPTG outside, although it benefits slighty when it is exposed to more. Note that the graphs color bar only extends from 55% of X production to 70% of X production. There appears to be no disernable effect in increasing the HSL outside, although when it is above 70,000 it seems to reduce the stochastic effects that stop the system lysing.

We now look at a graph showing HSL at values below 5000 molecules.

Input Model Graph 3.jpg

How we would like the system to run

Here are the following assumptions that need to make

KP has to be ~50 molecules per cell

KTetR has to be ~3000 molecules per cell

KCI has to be ~ 5000 molecules per cell

the input level of HSL has to be ~10,000 molecules

the input level of IPTG has to be ~5,000 molecules


Input Model Graph 12.jpg
Input Model Graph 13.jpg


How the system is expected to function

Input Model Graph 14.jpg