Introduction to modellingIn the process of designing our construct two major questions arose which could be answered by computer modelling:
- Output Amplification Model
We came up with an idea of using amplification of colour output to make it show within minutes after stimulus. The question that arose concerned deciding whether we should design the amplification module to be consisting of 1,2 or even more amplification steps. It appeared that the problem was recognised to be difficult enough to employ modelling.
- Protein Display Model
We came up with novel idea of detecting organisms that we do not have a specific receptor for. In the particular example that we have been considering, Schistosoma's protease was meant to cleave designed by us protein displayed on bacteria's cell wall. The cleaved peptide was supposed to be recognised by the receptor which would act to activate the colour expression. That solution raised questions about the risk of false positive or whether in there are any chances for ComD receptors to get activated in the diluted environment. Modelling was recognised as suitable to answer those questions.
To be changed
Model based on Michaelis Menten Kinetics
Comparison between different amplification models (HIV1 and TEV) based on Michaelis Menten kinetics. However, Michaelis Menten kinetics does not apply to our system. Therefore, it had to be modelled from first principle (see below using law of mass action).
Model based on Law of Mass Action
Comparison between these 3 different models: Simple production, 1-step and 2-step amplification.
Variables and Constants
Here are the variables and constants that are used in the Output Amplification Model.
Protein Display Model
This is a model showing when the ComD receptor will be activated (after proteins have been cleaved).
Variables and Constants
Here are the variables and constants that are used in the Protein Display Model.
Engineering approach to project
1. Influence of Specification on Design and vice versa:
- It was one of the longest steps as we were struggling to compromise the specifications with the viable designs.
2. Influence of Design on Modelling and vice versa:
- All modelling done was meant to give answers to questions that arose in the design phase.
- Once designs were chosen, they were modelled. It was found that 2 step amplification is not likely to be effiecient, so it was decided that only 1step amplification will be taken forward to assembly. This was a significant conclusion as it would take weeks in the labroatory to find that out.
- The doubt about big enough gradient of AIPs to be established in the extracellular space to set off receptor was rationalised by modelling. The model allowed to determine conditions for the system to work
3. Influence of Modelling on Assembly and vice versa:
- The results from modelling allowed to progress with assembly
4. Influence of Assembly on Testing and vice versa:
- testing has been planned ahead, so assembly contructs have been modified to allow some testing methods like: purification or negative control.
5. Influence of Testing on Specifications and vice versa:
- We did not get there yet. However, if the specifications would not be met by the results, we would need to try redesigning the system or, in case of no alternative, changing the specifications.
6. Influence of components not adjacent to each other in the cycle:
- Testing may influence modelling as the results of the two do not match.
- Many experiments were diesgned specifically on the request of modellers in order to find parameters for the models. Obtaining those paramters would increase the reliability of the models.