To produce PLPs, bacteria must contain both a helper phage (like M13KO7), that codes for the different phage proteins, and also a phagemid, that encodes the toxic gene we want to include in the PLP. If M13KO7 is packaged a replicative phage is produced, which we do not want, and if the phagemid it packaged then a PLP is produced.

The problem

Our objective is to produce phage like particles (PLP), for this, the bacteria must contain both a helper phage and also a phagemid (see figure). During phage production, several key events determine which DNA molecules are packaged into phage or PLP. These involve recognition of the M13 replication origin by several phage proteins.

A major hurdle to marketing KILL XYL is obtaining the necessary authorizations. Our interviews and legislation study both showed that the number of viable phages could be a problem. We therefore decided to measure and model the ratio between viable phage and phage-like particles, and so try to optimize this ratio to facilitate the preparation of pure PLP.

The Model

We based our model on a recently published model of "wild-type" M13 replication ^{[1] [2]}. This model was modified to incorporate: the helper-phage E. coli plasmid origin; the modification of the helper-phage M13 origin; the presence of a phagemid, with its own replicative origin and M13 origin. These modifications added xxx species, equations and yyy parameters to the original model. The modified model is available File:T--Aix-Marseille--Model.zip .

We used the initial measurement to constrain parameters of the model, along with published numbers for the number of copies of plasmids with different replicative origins.

Results

We need one or two graphs here showing how the packaging ratio depends on different parameters. A description of these graphs.

Conclusions

Clearly the initial design needs to be improved to increase the proportion of PLP produced. The model has shown as that the parameters of prime importance for determining the proportion of PLP produced are ....

1. ↑ Smeal et al, Simulation of the M13 life cycle I: Assembly of a genetically-structured deterministic chemical kinetic simulation, Virology, 500, January 2017
2. ↑ Smeal et al, Simulation of the M13 life cycle II: Investigation of the control mechanisms of M13 infection and establishment of the carrier state, Virology, 500, January 2017