Team:CIDEB-UANL Mexico/math overview

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<p>Where: “<i>a1</i>” means the transcription rate of a givengene; “<i>fy</i>” represents a regulatory function (if there is) that can activate or inhibit the system; and “<i>d1[mRNA]</i>” the degradation rate of the mRNA produced.</p>
<p>Where: “<i>a1</i>” means the transcription rate of a givengene; “<i>fy</i>” represents a regulatory function (if there is) that can activate or inhibit the system; and “<i>d1[mRNA]</i>” the degradation rate of the mRNA produced.</p>
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Revision as of 17:30, 14 June 2014

Overview Capture Aroma Resistance Union
iGEM CIDEB 2014 - Project

Overview

When Biology Meets Math

For iGEM projects, the use of mathematical models is performed to describe the behavior of biological systems, representing the quantitative relations between two or more variables involved in the function of gene(s) in organisms as E. coli.

Our team decided to use a deterministic model to simulate and represent the functioning of the four modules assuming that the variables (mRNA and protein concentrations) adopt a continuous behavior and obey kinetic rules that can be represented with constant values (Loera, 2012).

This type of mathematical model is used to involve variables that abstract both the gene expression and physiological cycles (chemical process, transport of proteins, etc.). By the use of traditional differential equations we were able to construct the description and analyze the behavior of mRNAs and proteins production. We were focused in determine through a mathematical model of the four modules (one per each): Capture, Aroma, Resistance and Union.

Deterministic Modelling: Equations and Parameters

As it was established previously, is necessary work with different equations focusing in the production rate and degradation rate according to the length of genes in each module of the project. This is performed in order to obtain both the concentration rates of mRNA and protein based on system (gene) length and protein length respectively.

Equations

● mRNA

Generally, to describe the amount of mRNA produced over t time, the equation implemented is shown below:

Where: “a1” means the transcription rate of a givengene; “fy” represents a regulatory function (if there is) that can activate or inhibit the system; and “d1[mRNA]” the degradation rate of the mRNA produced.

IMG_0317

● Protein

The same happens with the protein production, but differs in the formula because it also involves a posttranslational variable:

Where: “a2[mRNA]” means the translation rate of a protein based on the amount of mRNA available; “d2[P]” represents the degradation rate of that protein; and “f(post)" the posttranslational variables which affect the production of the final (functional) protein.

Parameters

To determine both the transcription (1) and translation (2) rates, we used the parameters from Singapore 2008 iGEM team, as well as the degradation rates from Beijing PKU 2009. We used the parameters for the speeds at which E. coli carries out transcription and translation from Singapore 2008 iGEM, assuming a transcription speed of 70nt/s and a translation speed of 40aa/s. We multiply the speeds by 60 because we use minutes as units in the simulations of the modules. We assumed that E. coli division time was 30min based on PKU Beijing 2009 iGEM team.

References

● Douglas Selinger, R. M. (2003). Global RNA Half-Life Analysis in Escherichia coli Reveals Positional Patterns of Transcript Degradation. Genome Research, 216-223.

● iGEM CIDEB UANL. (2012). Parameters. Retrieved on June 1st, 2014. From: https://2013hs.igem.org/Team:CIDEB-UANL_Mexico/Math-Equations.

● Loera, Miguel. (2012). “Representación matemática de circuitos genéticos”.

● PKU Beijing. (2009). Parameters. Retrieved on June 1st, 2014. From: https://2009.igem.org/Team:PKU_Beijing/Modeling/Parameters.

● Singapore. (2008). Parameters. Retrieved on June 1st, 2014. From:https://2008.igem.org/Team:NTU-Singapore/Modelling/Parameter.

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