Team:Kent/Modeling


iGEM Kent 2015


Modeling

Modeling is important as it allows us to describe the system mathematically. If we change some of the parameters in our system we can see how this will affect the system, this is especially important when the some of the parameters are unknown. The main aim of our model is to demonstrate the production of our nanowires in an interactive and interesting way.



More to come soon...

Contents

Variables
Chapter 2
Chapter 3
Chapter 4
Chapter 5
References

Variables

Variable Description Value
1 Length of the observation box volume 3
4 Depth of the observation box volume 6
7 Height of the cell in observation volume 9
M Number of binding sites W
1 Initial number of particles 3
8 Length of each timestep 10
15 Persistence Length 17
15 Monomer radius 17
15 Binding radius 17
15 Diffusion coefficient of the chain after the chain has detached 17
Event Description Value
P(bind) Probability that a monomer, within range, will attach to the end of a chain 3
P(leave) Probability that a monomer will leave the cell from the inside 6
P(spawn) Probability that a monomer will be created at the end of each timestep 9
P(decay) Probability that any given monomer will decay at each timestep W
P(monomer detach) Probability that the last monomer on a chain will detach 3
P(anchor detach) Probability that the chain will detach from the membrane 10
P(fragment) Probability that a chain of j monomers will fragment 17

Observation Volume

We have taken a small proportion of the cell and the bulk outside of the cell and extrapolated it to represent the whole system.



The typical length of an E coli cell is \(L \approx 2 \mu m\) and the typical diameter, \(d \approx 1 \mu m\). If we consider the cell to be composed of a cylinder of length \(l=L-d\) and two hemispheres at each end then the volume of the sphere is:



\[V_{cell} = V_{cylinder} + V_{sphere}\]
\[V_{cell} = \pi \big(\frac{d}{2}\big)^2 (L-d)+ \frac{4}{3} \pi \big(\frac{d}{2}\big)^3 = 1.309 (\mu m)^3\]

The volume of the cell inside the observation box is



\[V_{ob} = L_x L_y L_z = 0.08(\mu m)^3\]

From this we can work out the proportion of the volume of cell inside the observation box



\[\frac{V_{ob}}{V_{cell} } = 6.112%\]

Likewise for the surface area of the cell



\[A_{cell} = A_{cylinder} + A_{sphere}\]

\[A_cell = \pi d(L-d) + 4 \pi (\frac{d}{2})^2 = 6.28 (\mu m)^2 \]

The proportion of the cell's surface area inside the observation box is:



\[\frac{A_{ob}}{A_{cell}} = 2.54% \]

M

\[ \Delta x = \xi \sqrt{2D \Delta t} \] \[D(z) = c + \tanh(k(z - z_0)) \]

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E

\[ x' = \begin{cases}1 & -1 \le x < 0 \\ \frac{1}{2} & x = 0 \\ 1 - x^2 & \text{otherwise} \end{cases} \] \[ y' = \begin{cases}1 & -1 \le x < 0 \\ \frac{1}{2} & x = 0 \\ 1 - x^2 & \text{otherwise} \end{cases} \] \[z' = -z \] \[z' = 2 L_z - z \]

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S

\[ A + B \overset{k}{\rightarrow} AB\] \[ A_{j}B \overset{k_{+}}{\rightarrow} A_{j + 1}B \] \[ A_{j}B \overset{k_{-}}{\rightarrow} A_{i}B + A_{j-i} \] \[ \frac{\partial f(t,k)}{\partial t} = 2m(t) K_{+} f(t,j-1) - 2m(t)k_{+}f(t,j_ - k_{-}(j-1)f(t,j) + 2k_{-} \sum_{i=j+1}^\infty f(t,i) + k_{n}m(t)^{n_{c}} \delta _{j,n_{c}} (1) \] \[P = \sum_{j=n_c}^\infty f(t,j) \] \[M = \sum_{j=n_c}^\infty j * f(t,j) \] \[ <\cos (\alpha)> = \exp \big(- \frac{L}{\lambda } \big) = \exp \big(- \frac{jl}{\lambda} \big) \] \[ d_x = r \sin(\theta) \cos(\phi) \] \[ d_y = r \sin(\theta) \sin (\phi) \] \[ d_z = r \cos (\phi) \] \[ x = x_c + r \sin )\theta + \Delta \theta ) \cos (\phi + \Delta \phi \Delta t) \] \[ y = y_c + r \sin (\theta + \Delta \theta) \sin (\phi + \Delta \phi \Delta t) \] \[ z = z_c + r \cos (\theta + \Delta \theta ) \]

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Our Matlab code can be found here: Kent15_Model.m

References

Sivanathan, V., & Hochschild, A. (2012). Generating extracellular amyloid aggregates using E. coli cells. Genes & development, 26(23), 2659-2667.

Elowitz, M. B., Surette, M. G., Wolf, P. E., Stock, J. B., & Leibler, S. (1999). Protein Mobility in the Cytoplasm of Escherichia coli. Journal of bacteriology,181(1), 197-203.

Philipse, A. P. (2011). Notes on Brownian Motion. Utrecht University, Debye Institute, Van’t Hoff Laboratory.

Barlett, V. R., Hoyuelos, M., & Mártin, H. O. (2013). Monte Carlo simulation with fixed steplength for diffusion processes in nonhomogeneous media. Journal of Computational Physics, 239, 51-56.

Xue, W. F., Homans, S. W., & Radford, S. E. (2008). Systematic analysis of nucleation-dependent polymerization reveals new insights into the mechanism of amyloid self-assembly. Proceedings of the National Academy of Sciences,105(26), 8926-8931.

Knowles, T. P., Waudby, C. A., Devlin, G. L., Cohen, S. I., Aguzzi, A., Vendruscolo, M., ... & Dobson, C. M. (2009). An analytical solution to the kinetics of breakable filament assembly. Science, 326(5959), 1533-1537.