Difference between revisions of "Team:Queens Canada/Michaelis-Menten Kinetics"

Revision as of 05:41, 14 October 2018 (view source) Declanr (Talk | contribs) ← Older edit		Revision as of 05:41, 14 October 2018 (view source) Declanr (Talk | contribs) Newer edit →
Line 68:		Line 68:
	<h3 style="width:70%;margin-left:15%">Matlab Code</h3>		<h3 style="width:70%;margin-left:15%">Matlab Code</h3>
−	<pre class="prettyprint">	+	<pre class="prettyprint" style="width:70%;margin-left:15%">
	%********READ ME********		%********READ ME********

---

Revision as of 05:41, 14 October 2018

Michaelis-Menten Kinetics

Introduction

Michaelis - Menten kinetics is a model used to examine enzyme kinetic. Luciferase's activity can be modeled by Michaelis-Menten kinetics as they perform the simple conversion of a substrate into a product and a photon. Our project relied on the light producing NanoLuc Luciferase as a signal in our devices. We were able to model this relationship with MATLAB. The governing equations for this model were compiled in the MATLAB, with the goal of creating a generic calculator which teams may use in the future. Known values for concentrations and reactions rates are used as inputs, and the file produces the various rates of change with respect to the concentrations.

Governing Equations

The MATLAB code takes in the substrate concentration, product concentration, and enzyme concentration, represented as [S], [P] and [E] respectively. Additionally, known reaction rates for the forward, reverse, and catalytic directions are represented as k_f, k_r, and k_cat respectively. The preceding values are put into a function which generates the rates of change of concentration with respect to time through the following first order ordinary differential equations:

Application

We sought to apply the calculator generated here to model the Kinetics of NanoLuc Luciferase, our choice biosensor reporter. As can be seen from the graph generated by this calculator, and by the actual results obtained. NanoLuc Luciferase activity can be very accurately modeled with this tool, since its activity is substrate dependent, eventually reaching its maximum reaction rate when [S] >> [E].

Use

To use the calculator, simply open the MATLAB file and enter the reaction rates and concentration in the noted areas. After running the file, the reaction rates will appear in the MATLAB command window.

References

Beard, D [Daniel Beard]. (2014, 8 27). Enzyme Kinetics with MATLAB 2 [Video file]. Retrieved from https://www.youtube.com/watch?v=g-MApXluAaE&pbjreload=10

Matlab Code

%********READ ME********

%The following is a simple Michaelis–Menten rate of change calculator
%The commented out portion of the code is just the governing equations
%Fill in the parameters of dXdT in terms of s,p, and e
%Fill in the reaction rates (all set to 1 by default)
%The output will be the various rates

%Governing Equations

%E + S <> ES > E + P
%s=[S];  
%p=[P];
%e=[E];
%c=[ES];

%ds/dt = -kForward*e*s + kReverse*c
%dp/dt = kCat*c
%de/dt = -kForward*e*s + kReverse*c + kCat*c
%dc/dt = kForward*e*s - kReverse*c - kCat*c

%de/dt + dc/dt = 0
%d(e+c)/dt = 0

%E0 = e + c

%ds/dt = -kForward*e*s + kReverse*(E0-e)
%dp/dt = kCat*(E0-e)
%de/dt = -kForward*e*s + kReverse*(E0-e) + kCat*(E0-e)

s = 1; %Enter substrate concentration
p = 1; %Enter product concentration
e = 1; %Enter enzyme concentration



dXdT([s p e])

function [f] = dXdT(x)

kForward = 1; %Enter forward reaction rate
kReverse = 1; %Enter reverse reaction rate
kCat = 1;     %Enter catalytic reaction rate
E0 = 1;       %Enter initial concentration

s=x(1);
p=x(2);
e=x(3);

dsdt = -kForward*e*s + kReverse*(E0-e);
dpdt = kCat*(E0-e);
dedt = -kForward*e*s + kReverse*(E0-e) + kCat*(E0-e);

f = [dsdt; dpdt; dedt];
end

%***Acknowledgments***

%Daniel Beard - Enzyme Kinetics with MATLAB 2