Difference between revisions of "Team:UT-Tokyo/Model"

Line 81: Line 81:
 
== Abstract ==
 
== Abstract ==
 
<p>
 
<p>
 +
$$\frac{d[\sigma_A]}{dt}= \alpha \cdot\left(R_A+\frac{R_{td,A}\cdot [\mathrm{triggerRNA}]}{K^{\prime\prime}+[\mathrm{triggerRNA}]}\right)-\frac{\ln2}{\mathrm{HL}_{\sigma_A}}\cdot[\sigma_A]$$
 +
 
$$\frac{d[\sigma_A]}{dt}= \alpha \cdot\left(\frac{R_A+R_{td,A} [\mathrm{triggerRNA}]}{K^{\prime\prime}+[\mathrm{triggerRNA}]}\right)-\frac{\ln2}{\mathrm{HL}_{\sigma_A}}\cdot[\sigma_A]$$
 
$$\frac{d[\sigma_A]}{dt}= \alpha \cdot\left(\frac{R_A+R_{td,A} [\mathrm{triggerRNA}]}{K^{\prime\prime}+[\mathrm{triggerRNA}]}\right)-\frac{\ln2}{\mathrm{HL}_{\sigma_A}}\cdot[\sigma_A]$$
 
$$\frac{d[\sigma_B]}{dt}= \alpha\cdot \left(\frac{R_B+R_{td,B}\cdot [\mathrm{triggerRNA}]}{K^{\prime\prime}+[\mathrm{triggerRNA}]}\right)-\frac{\ln2}{\mathrm{HL}_{\sigma_B}}\cdot[\sigma_B]$$
 
$$\frac{d[\sigma_B]}{dt}= \alpha\cdot \left(\frac{R_B+R_{td,B}\cdot [\mathrm{triggerRNA}]}{K^{\prime\prime}+[\mathrm{triggerRNA}]}\right)-\frac{\ln2}{\mathrm{HL}_{\sigma_B}}\cdot[\sigma_B]$$

Revision as of 12:07, 19 October 2016

iGEM UT-TOkyo 2016


Transcription/lation Simulation

Abstract

We found some parameter sets on which E. coli changes gene expression by a generation. In addition, we also found ones on which circuit establishes the loops stably regardless of small fluctuation (noise in experiment). Therefore, our gene circuit seems likely to work as designed.

Introduction

We run a simulation about transcription and translation for two reasons. First is to make sure that our gene circuit functions as designed and establishes the loop of gene expression. Although the strain of E. coli used in our experiment, growing environment and sigma factors affect various parameter such as the speed of translation and transcription, and decomposition rate of factors, if there is no parameter sets which we need to establish the loop of gene expression of fluorescent protein, our project is theoretically impossible. In other words, to find the parameter set which establishes the loop means to show that our project is theoretically feasible. In addition, the simulation enables us to improve and redesign our gene circuit with reference to the parameter set.


The second purpose of simulation is to make sure whether the loop run correctly or not, when various parameters are found, such as the speed of translation and transcription, and decomposition rate of factors. If a tool is developed which calculate the movement of gene circuit according to the parameters found and outputs a graph of concentration change of fluorescent proteins, it enables us to decide whether the gene circuit run or not and choose the factor used in the experiment easily.

Method

variables character
sigma-factor A,B,C

$[\sigma_A], [\sigma_B], [\sigma_C]$

anti-sigma factor, A, B, C

$[\sigma_{-A}], [\sigma_{-B}], [\sigma_{-C}]$

mRNA of sigma factor A, B, C without toehold switch

$R_A, R_B, R_C$

mRNA of anti-sigma-factor A, B,C without toehold switch

$R_{-A}, R_{-B}, R_{-C}$

mRNA of sigma factor A, B, C with toehold switch

$R_{td, A}, R_{td, B}, R_{td, C}$

triggerRNA

$[\mathrm{taRNA}]$

arabinose

$[\mathrm{IPTG}]$

immature GFP, RFP, CFP

$[\mathrm{imGFP}], [\mathrm{imRFP}], [\mathrm{imCFP}]$

mature GFP, RFP, CFP

$[\mathrm{GFP}], [\mathrm{RFP}], [\mathrm{CFP}]$

mRNA of GFP, RFP, CFP

$R_{GFP}, R_{RFP}, R_{CFP}$

parameters character
proportionality constant of transcription rate

$k$

proportional constant of translation speed

$\alpha$

concentration of low copy plasmid

$C_{low}$

concentration of high copy plasmid

$C_{high}$

concentration of araC

$c_{araC}$

the dissociation constant between sigma-factor and sigma-promoter

$K$

the dissociation constant between araC and pbad operator

$K_{araC}$

the dissociation constant between sigma-factor and anti-sigma-factor

$K^{\prime}$

the dissociation constant between araC and arabinose

$K^{\prime}_{araC}$

the dissociation constant between toehold switch and triggerRNA

$K^{\prime\prime}$

half-life time of each substance

$\mathrm{HL}$

maturation time of fluorescent protein

$\mathrm{MT}$


Stability Analysis

Abstract

$$\frac{d[\sigma_A]}{dt}= \alpha \cdot\left(R_A+\frac{R_{td,A}\cdot [\mathrm{triggerRNA}]}{K^{\prime\prime}+[\mathrm{triggerRNA}]}\right)-\frac{\ln2}{\mathrm{HL}_{\sigma_A}}\cdot[\sigma_A]$$ $$\frac{d[\sigma_A]}{dt}= \alpha \cdot\left(\frac{R_A+R_{td,A} [\mathrm{triggerRNA}]}{K^{\prime\prime}+[\mathrm{triggerRNA}]}\right)-\frac{\ln2}{\mathrm{HL}_{\sigma_A}}\cdot[\sigma_A]$$ $$\frac{d[\sigma_B]}{dt}= \alpha\cdot \left(\frac{R_B+R_{td,B}\cdot [\mathrm{triggerRNA}]}{K^{\prime\prime}+[\mathrm{triggerRNA}]}\right)-\frac{\ln2}{\mathrm{HL}_{\sigma_B}}\cdot[\sigma_B]$$ $$\frac{d[\sigma_C]}{dt}= \alpha\cdot \left(\frac{R_C+R_{td,C}\cdot [\mathrm{triggerRNA}]}{K^{\prime\prime}+[\mathrm{triggerRNA}]}\right)-\frac{\ln2}{\mathrm{HL}_{\sigma_C}}\cdot[\sigma_C]$$ $$\frac{d[\sigma_{\mbox{-}A}]}{dt}= \alpha\cdot R_{\mbox{-}A}-\frac{\ln2}{\mathrm{HL}_{\sigma_{\mbox{-}A}}}[\sigma_{\mbox{-}A}]$$ $$\frac{d[\sigma_{\mbox{-}B}]}{dt}= \alpha\cdot R_{\mbox{-}B}-\frac{\ln2}{\mathrm{HL}_{\sigma_{\mbox{-}B}}}[\sigma_{\mbox{-}B}]$$ $$\frac{d[\sigma_{\mbox{-}C}]}{dt}= \alpha\cdot R_{\mbox{-}C}-\frac{\ln2}{\mathrm{HL}_{\sigma_{\mbox{-}C}}}[\sigma_{\mbox{-}C}]$$ $$\frac{dR_A}{dt}=k\cdot \mathrm{C}_{low}\cdot [\sigma_A]\cdot\frac{1-\frac{[\sigma_{\mbox{-}A}]}{K^{\prime}_a+[\sigma_{\mbox{-}A}]}}{K_a+[\sigma_A]\cdot\left(1-\frac{[\sigma_{\mbox{-}A}]}{K^{\prime}_a+[\sigma_{\mbox{-}A}]}\right)}+1-c_{araC}\cdot\frac{1-\frac{[\mathrm{IPTG}]}{K^{\prime}_{araC}+[\mathrm{IPTG}]}}{K_{araC}+c_{araC}\left(1-\frac{[\mathrm{IPTG}]}{K^{\prime}_{araC}+[\mathrm{IPTG}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_A$$ $$\frac{dR_B}{dt}=k\cdot \mathrm{C}_{low}\cdot [\sigma_B]\cdot\frac{1-\frac{[\sigma_{\mbox{-}B}]}{K^{\prime}_b+[\sigma_{\mbox{-}B}]}}{K_b+[\sigma_B]\cdot\left(1-\frac{[\sigma_{\mbox{-}B}]}{K^{\prime}_b+[\sigma_{\mbox{-}B}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_B$$ $$\frac{dR_C}{dt}=k\cdot \mathrm{C}_{low}\cdot [\sigma_C]\cdot\frac{1-\frac{[\sigma_{\mbox{-}C}]}{K^{\prime}_c+[\sigma_{\mbox{-}C}]}}{K_c+[\sigma_C]\cdot\left(1-\frac{[\sigma_{\mbox{-}C}]}{K^{\prime}_c+[\sigma_{\mbox{-}C}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_C$$ $$\frac{dR_{\mbox{-}A}}{dt}=k\cdot \mathrm{C}_{high}\cdot [\sigma_B]\cdot\frac{1-\frac{[\sigma_{\mbox{-}B}]}{K^{\prime}_b+[\sigma_{\mbox{-}B}]}}{K_b+[\sigma_B]\cdot\left(1-\frac{[\sigma_{\mbox{-}B}]}{K^{\prime}_b+[\sigma_{\mbox{-}B}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_{\mbox{-}A}$$ $$\frac{dR_{\mbox{-}B}}{dt}=k\cdot \mathrm{C}_{high}\cdot [\sigma_C]\cdot\frac{1-\frac{[\sigma_{\mbox{-}C}]}{K^{\prime}_c+[\sigma_{\mbox{-}C}]}}{K_c+[\sigma_C]\cdot\left(1-\frac{[\sigma_{\mbox{-}C}]}{K^{\prime}_c+[\sigma_{\mbox{-}C}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_{\mbox{-}B}$$ $$\frac{dR_{\mbox{-}C}}{dt}=k\cdot \mathrm{C}_{high}\cdot [\sigma_A]\cdot\frac{1-\frac{[\sigma_{\mbox{-}A}]}{K^{\prime}_a+[\sigma_{\mbox{-}A}]}}{K_a+[\sigma_A]\cdot\left(1-\frac{[\sigma_{\mbox{-}A}]}{K^{\prime}_a+[\sigma_{\mbox{-}A}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_{\mbox{-}C}$$ $$\frac{dR_{td,A}}{dt}=k\cdot \mathrm{C}_{low}\cdot [\sigma_C]\cdot\frac{1-\frac{[\sigma_{\mbox{-}C}]}{K^{\prime}_c+[\sigma_{\mbox{-}C}]}}{K_c+[\sigma_C]\cdot\left(1-\frac{[\sigma_{\mbox{-}C}]}{K^{\prime}_c+[\sigma_{\mbox{-}C}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_{td,A}$$ $$\frac{dR_{td,B}}{dt}=k\cdot \mathrm{C}_{low}\cdot [\sigma_A]\cdot\frac{1-\frac{[\sigma_{\mbox{-}A}]}{K^{\prime}_a+[\sigma_{\mbox{-}A}]}}{K_a+[\sigma_A]\cdot\left(1-\frac{[\sigma_{\mbox{-}A}]}{K^{\prime}_a+[\sigma_{\mbox{-}A}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_{td,B}$$ $$\frac{dR_{td,C}}{dt}=k\cdot \mathrm{C}_{low}\cdot [\sigma_B]\cdot\frac{1-\frac{[\sigma_{\mbox{-}B}]}{K^{\prime}_b+[\sigma_{\mbox{-}B}]}}{K_b+[\sigma_B]\cdot\left(1-\frac{[\sigma_{\mbox{-}B}]}{K^{\prime}_b+[\sigma_{\mbox{-}B}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_{td,C}$$ $$\frac{d[\mathrm{triggerRNA}]}{dt}=-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot [\mathrm{triggerRNA}]\ \textrm{(when Pnrd is on)}$$ $$\frac{d[\mathrm{IPTG}]}{dt}=-\frac{\ln2}{\mathrm{HL}_{IPTG}}\cdot [\mathrm{IPTG}]$$ $$\frac{d[\mathrm{imGFP}]}{dt}= \alpha\cdot [R_{\mathrm{GFP}}]-\frac{\ln2}{\mathrm{MT}_{GFP}}\cdot [\mathrm{imGFP}]-\frac{\ln2}{\mathrm{HL}_{imGFP}}\cdot [\mathrm{imGFP}]$$ $$\frac{d[\mathrm{imRFP}]}{dt}= \alpha\cdot [R_{\mathrm{RFP}}]-\frac{\ln2}{\mathrm{MT}_{RFP}}\cdot [\mathrm{imRFP}]-\frac{\ln2}{\mathrm{HL}_{imRFP}}\cdot [\mathrm{imRFP}]$$ $$\frac{d[\mathrm{imCFP}]}{dt}= \alpha\cdot [R_{\mathrm{CFP}}]-\frac{\ln2}{\mathrm{MT}_{GFP}}\cdot [R_{\mathrm{CFP}}]-\frac{\ln2}{\mathrm{HL}_{imCFP}}\cdot [\mathrm{imCFP}]$$ $$\frac{d[\mathrm{GFP}]}{dt}=\frac{\ln2}{\mathrm{MT}_{GFP}}\cdot [\mathrm{imGFP}]-\frac{\ln2}{\mathrm{HL}_{GFP}}\cdot [\mathrm{GFP}]$$ $$\frac{d[\mathrm{RFP}]}{dt}=\frac{\ln2}{\mathrm{MT}_{RFP}}\cdot [\mathrm{imRFP}]-\frac{\ln2}{\mathrm{HL}_{RFP}}\cdot [\mathrm{RFP}]$$ $$\frac{d[\mathrm{CFP}]}{dt}=\frac{\ln2}{\mathrm{MT}_{CFP}}\cdot [\mathrm{imCFP}]-\frac{\ln2}{\mathrm{HL}_{CFP}}\cdot [\mathrm{CFP}]$$ $$\frac{dR_{\mathrm{GFP}}}{dt}=k\cdot \mathrm{C}_{low}\cdot [\sigma_A]\cdot\frac{1-\frac{[\sigma_{\mbox{-}A}]}{K^{\prime}_a+[\sigma_{\mbox{-}A}]}}{K_a+[\sigma_A]\cdot\left(1-\frac{[\sigma_{\mbox{-}A}]}{K^{\prime}_a+[\sigma_{\mbox{-}A}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_{\mathrm{GFP}}$$ $$\frac{dR_{\mathrm{RFP}}}{dt}=k\cdot \mathrm{C}_{low}\cdot [\sigma_B]\cdot\frac{1-\frac{[\sigma_{\mbox{-}B}]}{K^{\prime}_b+[\sigma_{\mbox{-}B}]}}{K_b+[\sigma_B]\cdot\left(1-\frac{[\sigma_{\mbox{-}B}]}{K^{\prime}_b+[\sigma_{\mbox{-}B}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_{\mathrm{RFP}}$$ $$\frac{dR_{\mathrm{CFP}}}{dt}=k\cdot \mathrm{C}_{low}\cdot [\sigma_C]\cdot\frac{1-\frac{[\sigma_{\mbox{-}C}]}{K^{\prime}_c+[\sigma_{\mbox{-}C}]}}{K_c+[\sigma_C]\cdot\left(1-\frac{[\sigma_{\mbox{-}C}]}{K^{\prime}_c+[\sigma_{\mbox{-}C}]}\right)}-\frac{\ln2}{\mathrm{HL}_{RNA}}\cdot R_{\mathrm{CFP}} $$