Team:Paris/DryLab

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DryLab

Main

Questions

Our Message in a Bubble project aims at developing a communication system between bacteria. Among the various problems raised during the design phase, we investigated 3 of them with modeling and simulation:

• What is the link between Tol/Pal expression and vesicle formation? Or, more precisely, can we explain vesicule formation solely by the diffusion of the doubly anchored Tol/Pal complex in the membrane ? Understanding this connection is instrumental, since our project relies on the hypothesis that an increased in vesicle formation can be obtained simply by destabilization of the Tol/Pal complexes.

• How to improve the quality of the signal sent? Or more precisely, how can we get a good synchronization between the maximal production rate of vesicles and the maximal concentration of proteins to encapsulate ?

• How to optimize the quality of the reception? Or more precisely, how can we get a robust response despite a potentially very low number of signals (ie, vesicles) received ? Two characteristics of the response have been investigated: response amplitude and response time.

Results

• Understanding the link between Tol/Pal expression and vesicule formation

Overall, we showed that the formation of vesicles can be simply explained by the diffusion of Tol/Pal protein complexes. This very surprising result comes from 3 specific phenomena:

• The initial formation of small blebs can be explained by differences of osmotic pressures between intra- and extra-cellular environments, together with a non-perfectly uniform distribution of Tol/Pal complexes acting like press studs. (Details and figure 1)
• At the basis of nascent blebs, where the outer membrane is non-flat, the simple diffusion (ie Brownian motion) of doubly-anchored Tol/Pal molecules leads to their accumulation. (Details and figure 2)
• Rings of accumulated Tol/Pal at the basis of nascent blebs tend to constrict: vesiculation happens. This again simply results from plain Brownian motion on non-flat surfaces. (Details and figure 3)

Fig 2 here

Fig 3 here

• Improving the quality of the signal sent

In order to obtain a good synchronization between the maximal production rate of vesicles and the maximal concentration of proteins to encapsulate, we have to introduce a delay between the initiation of the synthesis of the proteins to encapsulate and the initiation of the synthesis of the truncated Tol protein that causes vesicle formation. We showed that this delay can be conveniently implemented by using a transcriptional cascade. More details here

• Optimizing the quality of message reception

Using stochastic simulations we identified two possible problems causing a non-robust response when the messenger concentration is low:

• the activation does not always occur
• even when it occurs, the activation time can vary significantly.

After trying various solutions, we found that an overexpression of the FecR protein solves both problems: simulations showed a good and robust activation in this case. More details here

Fig 5 here