Team:Colombia Uniandes/Scripting
From 2013.igem.org
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- | global gammaGR mGRIR mCC deltaGRI alfaR deltaR deltaCC betaCC k n deltaS H | + | %global gammaGR mGRIR mCC deltaGRI alfaR deltaR deltaCC betaCC k n deltaS H |
- | + | % | |
- | + | % | |
- | gammaGR= 0.1; %Diffussion rate of glucocorticoid inside the cell (mm/min) | + | gammaGR= 0.1; %Diffussion rate of glucocorticoid inside the cell (mm/min) |
- | mGRIR=1.080e-3; % GRI-R complex formation kinetic constant (1/umol min) | + | % |
- | mCC=1.14*10^-8; %GRI-R Complex formation reverse kinetic constant (1/min) | + | mGRIR=1.080e-3; % GRI-R complex formation kinetic constant (1/umol min) |
- | deltaGRI=0.00833; %Glucocorticoids Destruction rate inside the cell (1/min) | + | % |
- | alfaR= 0.8e3; %Basal production rate of the receptor (umol/min) | + | mCC=1.14*10^-8; %GRI-R Complex formation reverse kinetic constant (1/min) |
- | deltaR=0.004166; %Receptor destruction rate inside the cell (1/min) | + | % |
- | deltaCC=0.004166; % GRI-R complex Destruction rate (1/min) | + | deltaGRI=0.00833; %Glucocorticoids Destruction rate inside the cell (1/min) |
- | betaCC=0.5e3; % GRI-R complex maximum expression rate (umol/min) | + | % |
- | k=0.05e3; %Hill's constant for the GRI-R complex dimmer binding to his respective region (umol) | + | alfaR= 0.8e3; %Basal production rate of the receptor (umol/min) |
- | n=2; %Hill coefficient (cooperation constant) | + | % |
- | deltaS=0.04166; %Signal destruction rate (1/min) | + | deltaR=0.004166; %Receptor destruction rate inside the cell (1/min) |
- | H=2; %Correction constant for the signal | + | deltaCC=0.004166; % GRI-R complex Destruction rate (1/min) |
- | + | betaCC=0.5e3; % GRI-R complex maximum expression rate (umol/min) | |
- | + | k=0.05e3; %Hill's constant for the GRI-R complex dimmer binding to his respective region (umol) | |
- | + | n=2; %Hill coefficient (cooperation constant) | |
- | h=60; %Tiempo maximo | + | deltaS=0.04166; %Signal destruction rate (1/min) |
- | + | H=2; %Correction constant for the signal | |
- | m=0.01; %Longitud de paso [s] | + | % |
- | + | % | |
- | t=0:m:h; %Vector tiempo | + | % |
- | + | h=60; %Tiempo maximo | |
- | xi=[0 0 0 0]; | + | % |
- | + | m=0.01; %Longitud de paso [s] | |
- | y=fsolve(@CondIndGluco,xi,optimset('algorithm','levenberg-marquardt','maxiter',100000,'tolfun',1e-9)); | + | % |
- | + | t=0:m:h; %Vector tiempo | |
- | conInd=y; | + | % |
+ | xi=[0 0 0 0]; | ||
+ | % | ||
+ | y=fsolve(@CondIndGluco,xi,optimset('algorithm','levenberg-marquardt','maxiter',100000,'tolfun',1e-9)); | ||
+ | % | ||
+ | conInd=y; | ||
assignin('base','conInd',conInd); | assignin('base','conInd',conInd); | ||
l=(0:m:h)'; %Vector de tiempo | l=(0:m:h)'; %Vector de tiempo |
Revision as of 22:03, 25 September 2013
Scripting
Contents |
Glucocorticoid Detection System
Deterministic model
Equations
function y = EcuacionesGluco(t,x) global gammaGR mGRIR mCC deltaGRI alfaR deltaR deltaCC betaCC k n deltaS H
%---------Parameters------%
GRO=funcImpulso(t);
%------ Variables%------%
GRI= x(1); %Glucocorticoid inside the cell R=x(2); %Receptor in the cytoplasm CC=x(3); %Receptor -Glucocorticoid complex V=x(4); %Violacein
%---Equations---%
dGRI=gammaGR*(GRO-GRI)-mGRIR*GRI*R+mCC*CC-deltaGRI*GRI;
dR=alfaR-mGRIR*GRI*R+mCC*CC-deltaR*R;
dCC=mGRIR*GRI*R-mCC*CC-deltaCC*CC-(betaCC*CC.^n)/(k^n+CC.^n);%Revisar
dV=H*(betaCC*CC^n)/(k^n+CC^n)-deltaS*V;
y1(1)=dGRI; y1(2)=dR; y1(3)=dCC; y1(4)=dV;
y= y1';
end
Equation solver
%global gammaGR mGRIR mCC deltaGRI alfaR deltaR deltaCC betaCC k n deltaS H % % gammaGR= 0.1; %Diffussion rate of glucocorticoid inside the cell (mm/min) % mGRIR=1.080e-3; % GRI-R complex formation kinetic constant (1/umol min) % mCC=1.14*10^-8; %GRI-R Complex formation reverse kinetic constant (1/min) % deltaGRI=0.00833; %Glucocorticoids Destruction rate inside the cell (1/min) % alfaR= 0.8e3; %Basal production rate of the receptor (umol/min) % deltaR=0.004166; %Receptor destruction rate inside the cell (1/min) deltaCC=0.004166; % GRI-R complex Destruction rate (1/min) betaCC=0.5e3; % GRI-R complex maximum expression rate (umol/min) k=0.05e3; %Hill's constant for the GRI-R complex dimmer binding to his respective region (umol) n=2; %Hill coefficient (cooperation constant) deltaS=0.04166; %Signal destruction rate (1/min) H=2; %Correction constant for the signal % % % h=60; %Tiempo maximo % m=0.01; %Longitud de paso [s] % t=0:m:h; %Vector tiempo % xi=[0 0 0 0]; % y=fsolve(@CondIndGluco,xi,optimset('algorithm','levenberg-marquardt','maxiter',100000,'tolfun',1e-9)); % conInd=y;
assignin('base','conInd',conInd); l=(0:m:h)'; %Vector de tiempo
x=zeros(length(l),length(conInd)); %Matriz de variables, en las columnas varia %la variable y en las filas varia el tiempo
GRO=zeros(1,length(l));
x(1,:)=conInd;
for u=1:length(l)-1
xk=x(u,:); %Captura de la ultima posicion de la matirz, es decir, los %valores actuales de las variables k1=EcuacionesGluco(l(u),xk); %Primera pendiente del metodo de RK4 k2=EcuacionesGluco(l(u)+m/2,xk+(m/2*k1)'); %Segunda pendiente del metodo de RK4 k3=EcuacionesGluco(l(u)+m/2,xk+(m/2*k2)'); %Tercera pendiente del metodo de RK4 k4=EcuacionesGluco(l(u)+m,xk+(m*k3)'); %Cuarta pendiente del metodo de RK4 xk1=xk+m/6*(k1+2*k2+2*k3+k4)'; %Calculo de nuevos valores para las %variables xk2=zeros(1,length(xk1)); for p=1:length(xk1) if(xk1(p)<0.00000001) xk2(p)=0; else xk2(p)=xk1(p); end end x(u+1,:)=xk2; %Actualizacion del nuevo vector de variables en la matriz
end
for j=1:length(l)
if (l(j)<(10) || l(j)>(30)) GRO(j)=155; else GRO(j)=155*1.3; end
end
GRI=x(:,1); R=x(:,2); CC=x(:,3); V=x(:,4);
figure(1)
plot(l,R)%,l,GRO)%,l,CC,l,V)
legend('Receptor')%,'Glucocorticoid') %, 'Complex', 'Signal')
xlabel('Time')
ylabel('Concetration (micromolar)')
title('Glucocorticoid model')
figure(2) plot(l,CC)%,l,GRO) legend('Complejo')%,'Glucocorticoid')
figure(3) plot(l,V)%,l,GRO) legend('Senal')%,'Glucocorticoid')
figure(4) plot(l,GRI)%,l,GRO) legend('GRI')%,'Glucocorticoid')
Stochastic
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