Team:TU-Delft/Timer-Sumo-KillSwitch

Timer-SUMO-KillSwitch

The separate modules: Timer plus SUMO and Kill Switch are combined to form the complete model of the system: Timer - SUMO - Kill Switch. For the final model, the kill switch module is converted in such a way so as the holin and antiholin to be activated by the Pci promoter.

Figure 1: Circuit of the kill switch

Differential Equations

Parameters

Parameter	Value	Description	Units	Reference
ca	1020	Translation rate per amino acid	min-1#a-1	[7]
cT7	4.16	Maximum transcription rate of T7	#m/min	[2]
cptet	2.79	Maximum transcription rate of Ptet	#m/min	[4]
cpconst	0.5	Transcription rate of Pconst	#m/min	Assumption
cci	1.79	Maximum transcription rate of Pci	#m/min	[3]
dmRNA	0.231	Degradation rate of mRNA	min-1	[8]
dH	0.0348	Degradation rate of holin / Antiholin	M/min	[17]
dTET	0.1386	Degradation rate of TET	min-1	[9]
dCI	0.042	Degradation rate of CI	min-1	[9]
kb,HAH	0.3*10-4	Backward rate		[17]
kf,HAH	11.7*10-4	Forward rate		[17]
dPEP	2.1*10-3	Degradation rate of the peptide	min-1	Assumed three times slower same as GFP
dPSU	6.3*10-3	Degradation rate of the peptide plus SUMO	min-1	Assumed the same as GFP
dUlp	1.263*10-2	Degradation rate of Ulp	min-1	Assumed twice the rate of GFP
lt7	0.002	Leakage factor of T7	-	Assumption
lptet	0.002	Leakage factor of Ptet	-	Assumption
lci	0.002	Leakage factor of Pci	-	Assumption
ktet	6	Dissociation constant of Ptet	#m	[10]
kci	20	Dissociation constant of Pci	#m	[10]
kcUlp	3	Turnover rate of Ulp	min-1	[6]
nci	3	Hills coefficient	-	[11]
ntet	3	Hills coefficient	-	[11]
s	0 or 1	Activation/Inactivation of T7 promoter	Binary	Assumption
sci	228	Length of CI	amino acids	[12]
sPSU	18 + 110	Length of peptide plus SUMO	amino acids	[12]
sTET	206	Length of TET	amino acids	[13]
sUlp	233	Length of Ulp1	amino acids	[13]
sH	219	Length of Holin	amino acids
sAH	103	Length of Antiholin	amino acids

Results

In Figure 1 the results of the simulation are shown.

Figure 1: Simulation Results

Conclusion/Discussion

In Figure 1 the behavior of the total circuit is seen, and the answers to the questions can be given:

1. How many minutes does the cell lysis take from the point of induction?
   After 165 minutes the Holin concentration passes 190 molecules per cell and cell lysis occurs.
2. How much peptides are produced by the circuit?
   The total concentration is 18000 peptides per cell.
3. How much peptides are still uncleaved by the SUMO at the point of cell lysis?
   The models shows that there is almost no SUMO-peptide uncleaved.

Sensitivity analysis

To asses the validity of the found answers a sensitivity analysis is performed. In this case the numerical derivative of the solution is taken with respect to the parameters of the model. This derivative represents the change of the solution upon changing the specific parameter. If this change is large, the solution is very sensitive for this parameter. Also, since the solution is highly non-linear this numerical derivative is taken in both directions, as they differ greatly in this model. To compare the found values of the derivative, they are normalized by the nominal value (the solution, e.g. the lyse time). In this way a percentual change is found. Mathematically this can be expressed as:

So, for the three answers the sensitivity analysis is done, yielding the follow results and conclusions:

1. The lysis time is not significantly affected by most parameters, only two are important. The degradation rate of cI has the most influence, the relative sensitivity is around 80%. This is logical, because this is of major influence on the timer, as the timer is determined by the time cI takes to degrade. In the same way, the CcI, the expression rate of the cI promotor also influences the lysis time. The cpconst also has a significant influence, a relative sensitivity of around %, which is explained by the fact that the expression rate changes the speed of the production of anti-holin and thus the lysis time. What is interesting is that the dimerization parameters do not hold a major influence, as well as the degradation rates of holin and anti-holin.
2. The total amount of produced peptide is influenced by almost every parameter. The most significant ones are the expression strength of the T7 promoter and the degradation rate of the mRNA, both having a relative sensitivity of over 100%.
3. The amount of uncleaved peptide is also influenced by a lot of parameters, however the relative sensitivity is always below 200%. This might seem a lot, but the concentration is virtually zero thus these influences can be neglected. It is safe to say that except for very large changes, the conclusion will hold that there is almost no uncleaved peptide.