Difference between revisions of "Team:Technion HS Israel/Modelling/Equations"
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− | Full equations | + | <h1>Full equations </h1> |
− | 1 Notations | + | <h2>1 Notations</h2> |
− | 1.1 Notation principles | + | <h3>1.1 Notation principles</h3> |
− | Every relevant substance in the cell is denoted with uppercase | + | <p>Every relevant substance in the cell is denoted with uppercase |
letters which describes the substance, and a subscript which | letters which describes the substance, and a subscript which | ||
encodes the scale in which the amount of the substance is | encodes the scale in which the amount of the substance is | ||
− | measured by the variable. For example, if we have a substance Y, | + | measured by the variable. For example, if we have a substance Y, </p> |
− | + | <ul> | |
− | + | <li> its amount inside a single cell is denoted by Y_{in}</li> | |
− | + | <li> its amount inside all the cells together (its total amount | |
− | inside the cells) is denoted by Y_{sum} | + | inside the cells) is denoted by Y_{sum}</li> |
− | + | ||
− | + | <li> its amount outside all the cells (its external amount) is | |
− | denoted by Y_{out} | + | denoted by Y_{out}</li> |
− | + | ||
− | 2 A list of all the notations we used | + | </ul> |
+ | <h2>2 A list of all the notations we used</h2> | ||
− | Substances: | + | <h3>Substances:</h3> |
− | + | <ul> | |
− | A | + | <li>A |
- AHL (The auto inducer, a short for N-Acyl homoserine | - AHL (The auto inducer, a short for N-Acyl homoserine | ||
− | lactone). | + | lactone).</li> |
− | L - LuxR (a transciptional activator protein) | + | <li>L - LuxR (a transciptional activator protein)</li> |
− | LA - the complex LuxR and AHL form together. | + | <li>LA - the complex LuxR and AHL form together.</li> |
− | LA_{2} | + | <li>LA_{2} |
- the dimer we get when two LuxR-AHL complexes bind | - the dimer we get when two LuxR-AHL complexes bind | ||
− | together. | + | together.</li> |
− | aa - Aiia (a AHL-lactonase). | + | <li>aa - Aiia (a AHL-lactonase).</li> |
− | a_{1} | + | <li>a_{1} |
− | - plasmids with an unactivated LuxR promotor. | + | - plasmids with an unactivated LuxR promotor.</li> |
− | a_{2} | + | <li>a_{2} |
− | - plasmids with an activated LuxR promotor. | + | - plasmids with an activated LuxR promotor.</li> |
− | TRLV - | + | <li>TRLV -<font color="red">NOTICE IM EMPTY??</font> </li> |
− | b_{1} | + | <li>b_{1} |
− | - plasmids with an unactivated Tet promotor. | + | - plasmids with an unactivated Tet promotor.</li> |
− | b_{2} | + | <li>b_{2} |
− | - plasmids with an activated Tet promotor. | + | - plasmids with an activated Tet promotor.</li> |
− | ccbd - Toxin we use to kill the cell. | + | </li>ccbd - Toxin we use to kill the cell.</li> |
− | X - any gene we want to measure the amount of it that will be | + | <li>X - <p>any gene we want to measure the amount of it that will be |
produced by the bacteria colony. For example, it might represent | produced by the bacteria colony. For example, it might represent | ||
− | the amount of a certain drug the bacteria produce. | + | the amount of a certain drug the bacteria produce.</p></li> |
+ | </ul> | ||
− | Other quantitie of interest: | + | <h3>Other quantitie of interest:</h3> |
+ | <ul> | ||
− | N - number of bacteria. The bacteria are divided to two groups | + | <li>N - number of bacteria. The bacteria are divided to two groups</li> |
N^{+} | N^{+} |
Revision as of 19:03, 15 September 2015
Full equations
1 Notations
1.1 Notation principles
Every relevant substance in the cell is denoted with uppercase letters which describes the substance, and a subscript which encodes the scale in which the amount of the substance is measured by the variable. For example, if we have a substance Y,
- its amount inside a single cell is denoted by Y_{in}
- its amount inside all the cells together (its total amount inside the cells) is denoted by Y_{sum}
- its amount outside all the cells (its external amount) is denoted by Y_{out}
2 A list of all the notations we used
Substances:
- A - AHL (The auto inducer, a short for N-Acyl homoserine lactone).
- L - LuxR (a transciptional activator protein)
- LA - the complex LuxR and AHL form together.
- LA_{2} - the dimer we get when two LuxR-AHL complexes bind together.
- aa - Aiia (a AHL-lactonase).
- a_{1} - plasmids with an unactivated LuxR promotor.
- a_{2} - plasmids with an activated LuxR promotor.
- TRLV -NOTICE IM EMPTY??
- b_{1} - plasmids with an unactivated Tet promotor.
- b_{2} - plasmids with an activated Tet promotor. ccbd - Toxin we use to kill the cell.
- X -
any gene we want to measure the amount of it that will be produced by the bacteria colony. For example, it might represent the amount of a certain drug the bacteria produce.
Other quantitie of interest:
- N - number of bacteria. The bacteria are divided to two groups N^{+} - bacteria with our plasmid. N^{-} - bacteria without our plasmid (in other words, bacteria that lost the plasmids we introduced into them). V - volume of the relevant scale. That means, V_{out} - the volume of the space outside the cells. V_{sum} - the volume of the total space inside all the cells. w - width of the cell membrane. Constants C1 - C18 - different reaction constants. T^{+} - plamid positive generation time. T^{-} - plamid free generation time. p - the chance to loose a plasmid. D- AHL diffusion constant. 3 Reactions \frac{dA_{out}}{dt}=-D(\frac{A_{out}}{V_{out}}-\frac{A_{sum}}{V_{sum}})(N^{+}+N^{-}) \frac{dA_{sum}}{dt}=D(\frac{A_{out}}{V_{out}}-\frac{A_{sum}}{V_{sum}})N^{+}-\frac{c_{1}aa_{in}A_{sum}}{c_{18}+A_{in}}+c_{4}LA_{sum}-(c_{3}L_{in}\cdot A_{sum})-c_{2}A_{sum} \frac{dLA_{sum}}{dt}=c_{3}L_{in}\cdot A_{sum}-c_{4}LA_{sum}-2(c_{5}LA_{sum}LA_{in}-c_{6}LA_{2,sum}) \frac{dLA_{2,sum}}{dt}=c_{5}LA_{sum}LA_{in}-c_{6}LA_{2,sum}-(c_{7}a_{0,in}LA_{2,sum}-c_{8}a_{1,sum}) \frac{d(a_{0,in}+a_{1,in})}{dt}=0 \frac{da_{1,in}}{dt}=c_{7}a_{0,in}LA_{2,in}-c_{8}a_{1,in} \frac{dTRLV_{sum}}{dt}=A_{RBS}\cdot(a_{0,sum}v_{0}+a_{1,sum}v_{1})-c_{9}TRLV_{sum}-(c_{1}b_{0,in}TRLV_{sum}-c_{11}b_{1,in}) \frac{d(b_{0,in}+b_{1,in})}{dt}=0 \frac{db_{1,in}}{dt}=c_{1}b_{0,in}TRLV_{in}-c_{11}b_{1,in} \frac{dccdb_{sum}}{dt}=B_{RBS}\cdot(b_{0,sum}u_{0}+b_{1,sum}u_{1})-c_{12}ccdb_{sum} \frac{dx_{tot}}{dt}=c_{13}N^{+} \frac{dL_{sum}}{dt}=c_{14}N^{+}-c_{15}L_{sum}-(c_{3}L_{in}\cdot A_{sum}-c_{4}LA_{sum}) \frac{daa_{sum}}{dt}=c_{16}N^{+}-c_{17}aa_{sum} \frac{dN^{+}}{dt}=\frac{ln(2-p)}{T^{+}}N^{+}(1-\frac{N^{+}+N^{-}}{N_{max}}) \frac{dN^{-}}{dt}=\frac{ln2}{T^{-}}N^{-}(1-\frac{N^{+}+N^{-}}{N_{max}})+\frac{ln2-ln(2-p)}{T^{+}}N^{+} With some assumptions Assumptions 4 section \frac{dA_{out}}{dt}=-(\frac{A_{out}}{V_{out}}-\frac{A_{sum}}{V_{sum}})(N^{+}+N^{-})c_{20}Area_{in} \frac{dA_{sum}}{dt}=(\frac{A_{out}}{V_{out}}-\frac{A_{sum}}{V_{sum}})N^{+}c_{20}Area_{in}-\frac{c_{1}aa_{in}A_{sum}}{c_{18}+A_{in}}-(c_{3}L_{in}\cdot A_{sum}) \frac{dLA_{sum}}{dt}=c_{3}L_{in}\cdot A_{sum}-2(c_{5}LA_{sum}LA_{in}-c_{6}LA_{2,sum}) \frac{dLA_{2,sum}}{dt}=c_{5}LA_{sum}LA_{in}-c_{6}LA_{2,sum} \frac{d(a_{0,in}+a_{1,in})}{dt}=0 \frac{da_{1,in}}{dt}=c_{7}a_{0,in}LA_{2,in}-c_{8}a_{1,in} \frac{dTRLV_{sum}}{dt}=A_{RBS}\cdot(a_{0,sum}v_{0}+a_{1,sum}v_{1}) \frac{d(b_{0,in}+b_{1,in})}{dt}=0 \frac{db_{1,in}}{dt}=c_{1}b_{0,in}TRLV_{in}-c_{11}b_{1,in} \frac{dccdb_{sum}}{dt}=B_{RBS}\cdot(b_{0,sum}u_{0}+b_{1,sum}u_{1})-c_{12}ccdb_{sum} \frac{dx_{tot}}{dt}=c_{13}(N^{+}+N^{-}) \frac{dL_{sum}}{dt}=c_{14}N^{+}-(c_{3}L_{in}\cdot A_{sum}-c_{4}LA_{sum}) \frac{daa_{sum}}{dt}=c_{16}N^{+} \frac{dN^{+}}{dt}=\alpha^{+}N^{+}(1-\frac{N^{+}+N^{-}}{N_{max}})(1-\mu) \frac{N^{-}}{dt}=\alpha^{-}N^{-}(1-\frac{N^{+}+N^{-}}{N_{max}})+\alpha^{+}N^{+}(1-\frac{N^{+}+N^{-}}{N_{max}})(1-\mu) Initial conditions ----- AHL_{out} - how much AHL we put. a0 - initial number of strands (probably plasmid number). a1 - 0. b0 - initial number of strands (probably plasmid number). Sounds equal to a_{0}(t=0) . b1 - 0. N^{+} - the number of cells we have at the beginning. N^{-} - 0. all the rest - 0. Ways to compute things \alpha^{+}=\frac{1-p}{T^{+}}+\frac{p}{T^{-}} \mu=1-\frac{ln(2-x)}{ln2} \alpha^{-}=\frac{2^{\frac{T^{+}}{T^{-}}}-1}{T^{-}} Sub_{sum}=N^{+}Sub_{in} V_{out}\sim V_{tot} Things to talk about • The way I took into account the plasmid-less bacteria. • Mistakes in first equation and what used to be the last one. • Meaningful names. • RNA transcription. In other places, they replace (5-7) with this: \frac{dTRLV}{dt}= • Validity of the plasmid loss computations.