Model for tRNA amber diffusion system

Summary

The tRNA amber diffusion design is the design we have using the smallest molecule we want to diffuse through nanotubes: tRNA. The emitter cell produces this tRNA amber which is transfered through nanotubes and serves to translate the so-called mRNA amber (mRNA for T7 RNA polymerase with two amber mutations). This mRNA amber can be translated only in presence of our mutant tRNA and is therefore our receptor construct. Having two amber mutations in the T7 RNA polymerase gene in the receiver cell should prevent any leakiness from the receiver construct. The auto-amplification is obtained through the same T7 auto-amplification loop used in the T7 RNA polymerase diffusion design.

The behaviour expected is to have an ON/OFF switch activating when a certain number of tRNA amber have entered the cell. To be certain this activation was possible, we ran additionnal simulation of tRNA diffusion in one cell. Our conclusion was that a delay of a less than 10 minutes might be observed in the receiver cell if very few tRNA amber arrive in the receiver cell. You can find more about this sub-model here.

You will find below the results for a simple simulation with every part of the design in one cell. All of our components are in one cell. Between t=7500s and t=12500s, IPTG is added to the cell, lifting repression by LacI. RFP is the reporter for the emitting construct and GFP for the receiving construct.

Fig1: Matlab simulation for the tRNA amber construct (all in one cell, only reporters molecules and IPTG input)

Our simulation exhibits the behaviour we expected. The model shows that in our experimental conditions the cell should produce a significant response in a reasonable time (approximately 20 to 30 minutes after the tRNA amber appears in the cell). Once started, the auto-amplification loop can not be stopped, as we can see with the GFP staying at its maximum even when RFP levels decrease. The major limit of this model could come from leakiness of promoters. If the pT7 is not as reliable as we thought, the auto-amplification loop could trigger itself all the time.

Even though the timescale for tRNA amber diffusion in the receiver cell is reasonable, we tried several possible stable states of tRNA amber input for the receiver construct. This stable state hypothesis for tRNA amber is justified by the recycling of tRNA in the cells.

Design

The tRNA amber diffusion design is the design we have using the smallest molecule we want to diffuse through nanotubes: tRNA. The emitter construct produces tRNA amber a tRNA which is complementary to amber stop codons but transports an amino-acid (TO BE COMPLETED) instead of stopping translation. tRNA amber is then transfered through the nanotubes and into the receiver cell.

In the receiver cell, a T7 RNA polymerase amber gene constitutively produces the so-called mRNA amber (mRNA for T7 RNA polymerase with two amber mutations) which is our receiver construct. This mRNA amber can be translated into functional T7 RNA polymerase only in presence of our mutant tRNA amber. We note the functional polymerases expressed from this gene T7 amber.

The amplifier construct is then a T7 auto-amplifying loop identical to the one in the T7 RNA polymerase diffusion design. The T7 amber activates this loop which is also where our reporter GFP is expressed.

This construction was put in two different settings. One is what we just described, where the emitting gene network is in one cell and the receiving gene network is in another. In the other construction, everything is in one cell. We use the second construct as a control to really see the impact of the cell-to-cell communication on the behaviour of the cells.

We ran our models for those two configurations. We used a steady flow of signaling molecules in the receiver cell for the "one emitting cell - one receiving cell" construction. You can find our justifications about this assumption here.

Model

LacI

We use LacI as a repressor for the emitter gene construct. LacI repression can be cancelled by IPTG. This way we can induce production of RFP and tRNA amber by adding IPTG on the cells.

Inactivated LacI can not repress the pLAC promoter anymore. Note that we consider that the reaction between IPTG and LacI fires without any delay. This assumption is justified by the fact that this reaction is much faster than any other in our gene network.

Emitter gene construct - tRNA amber

The emitter gene construct is modeled by the following equations:

The reporter for the emitter gene construct (RFP) is modeled by the following equations:

Receiver gene construct - T7 amber

The receiver gene construct is modeled by the following equations:

You will remark that activated mRNA amber is noted mRNA^* amber. This corresponds simply to mRNA_amber being translated into functional T7 RNA polymerase using two tRNA amber. Since we have hints that tRNA amber are used pretty quickly in the translation process (see tRNA diffusion in one cell) we used a very simple equation to model this:

Amplifier gene construct - T7 auto-amplification loop

The amplifier gene construct is modeled by the following equations:

The reporter for the amplification (and indirectly for the receiver) gene construct (GFP) is modeled by the following equations:

Parameters

This design relies on tRNA amber as the signaling molecule going through the nanotubes.

The parameters used in this model are:

Description	Value	Unit	Reference
Active LacI concentration (LacI which is not inactivated by IPTG)	NA	molecules per cell	Notation convention
IPTG concentration	NA	molecules per cell	Notation convention
Inactivated LacI concentration	NA	molecules per cell	Notation convention
Total LacI concentration	TBD	molecules per cell	Steady state for equation
tRNA amber concentration	NA	molecules per cell	Notation convention
mRNA amber concentration	NA	molecules per cell	Notation convention
Translated mRNA amber concentration	NA	molecules per cell	Notation convention
T7 amber concentration	NA	molecules per cell	Notation convention
mRNA associated with T7 (non amber, amplification) concentration	NA	molecules per cell	Notation convention
T7 (non amber, amplification) concentration	NA	molecules per cell	Notation convention
Maximal production rate of pVeg promoter (constitutive)	0.02	molecules.s^-1 or pops	Estimated, see the justification
Maximal production rate of pLac promoter	0.02	molecules.s^-1 or pops	Estimated, see the justification
Maximal production rate of pT7 promoter	0.02	molecules.s^-1 or pops	Estimated, see the justification
Dissociation constant for IPTG to LacI	1200	molecules per cell	Aberdeen 2009 wiki
Dissociation constant for LacI to LacO (pLac)	700	molecules per cell	Aberdeen 2009 wiki
Dissociation constant for T7 RNA polymerase to pT7	10	molecules per cell	We used the classic assumption 1nM=1 molecule per cell and http://www.ncbi.nlm.nih.gov/pmc/articles/PMC309671/pdf/nar00061-0090.pdf
Translation rate of proteins	0.9	s^-1	Estimated, see the justification
Dilution rate in exponential phase	2.88x10^-4	s^-1	Calculated with a 40 min generation time. See explanation
Degradation rate of mRNA	2.88x10^-3	s^-1	Uri Alon (To Be Confirmed)
Delay due tT7 RNA polymerase production and maturation	300	s	http://mol-biol4masters.masters.grkraj.org/html/Prokaryotic_DNA_Replication13-T7_Phage_DNA_Replication.htm
Delay due to mRNA production	30	s	http://bionumbers.hms.harvard.edu/bionumber.aspx?s=y&id=104902&ver=5&hlid=58815 2kb/(50b/s) --> approximation: all our contructs are around 2kb