- Author:
- pmr2.import <nobody@models.cellml.org>
- Date:
- 2009-04-29 23:49:20+12:00
- Desc:
- committing version03 of elowitz_leibler_2000
- Permanent Source URI:
- https://models.physiomeproject.org/workspace/elowitz_leibler_2000/rawfile/dddf77806817cf15840692646945a1a3c001fb27/elowitz_leibler_2000.cellml
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<title>A synthetic oscillatory network of transcriptional regulators. </title>
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<firstname>Jeelean</firstname>
<surname>Lim</surname>
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<shortaffil>Bioengineering Institute, University of Auckland</shortaffil>
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<title>Model Status</title>
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This CellML version of the model has been checked PCEnv and the model runs to replicate the original published results as depicted in figure 1c of the paper. The units have been checked and are consistent.
</para>
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<title>Model Structure</title>
<para>
ABSTRACT: Networks of interacting biomolecules carry out many essential functions in living cells, but the 'design principles' underlying the
functioning of such intracellular networks remain poorly understood, despite intensive efforts including quantitative analysis of relatively simple systems. Here we present a complementary approach to this problem: the design and construction of a synthetic network to implement a particular function.
</para>
<para>
We used three transcriptional repressor systems that are not part of any natural biological clock to build an oscillating network, termed
the repressilator, in Escherichia coli. The network periodically induces the synthesis of green fluorescent protein as a readout of
its state in individual cells. The resulting oscillations, with typical periods of hours, are slower than the cell-division cycle, so the
state of the oscillator has to be transmitted from generation to generation. This artificial clock displays noisy behaviour, possibly
because of stochastic fluctuations of its components. Such 'rational network design' may lead both to the engineering of
new cellular behaviours and to an improved understanding of naturally occurring networks.
</para>
<para>
The complete original paper reference is cited below:
</para>
<para>
<ulink url="http://www.nature.com/nature/journal/v403/n6767/full/403335a0.html">A synthetic oscillatory network of transcriptional regulators</ulink>, Michael B. Elowitz and Stanislas Leibler, 2000, <ulink url="http://www.nature.com/nature/index.html">
<emphasis> Nature: International Weekly Journal of Science</emphasis>
</ulink>, 403, 335-338. (A <ulink url="http://www.nature.com/nature/journal/v403/n6767/pdf/403335a0.pdf">PDF version</ulink> of the article is available to subscribers on the journal website.) <ulink url="http://www.ncbi.nlm.nih.gov/pubmed/10659856">PubMed ID: 10659856</ulink>
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<rdf:value>There was an error in rescaling previously:
m in the equations in box 1 is not rescaled to the mRNA divided by the translation efficiency, M/eff, but is just M*eff/K_m, with the efficiency taken in units of rescaled protein p = P/K_m.
The 2 forms of the differential equations are therefore:
dM_i/dt = K_m/(eff*tavg) * alpha * Km^n/(Km^n+P_j^n) + alpha0 - M_i/tavg
and
dPi/dt = beta*(Mi*eff/tavg - Pi/tavg)
Rescaled protein numbers were also used for the alphas:
beta = proteindecay/mRNAdecay = rnahalflife/proteinhalflife = 0.2
and
alpha0 = number of maximal rescaled proteins per cell in steady state under full repression:
with a0 = leaky promotor strength = 5*10^-4 mRNA per second
max. translation = eff*a0
protein decay = Pi/average_protein_lifetime
in steady state: max. translation = protein decay =>
P_max = eff*a0*average_protein_lifetime(in seconds) = 20*5*10^(-4)*10/ln(2)*60 = 8.656
alpha0 = p_max = P_max/K_m = 0.216
and for the completely repressor free state:
a = fully induced promotor strength = 0.5 mRNAs per second
P_max= 20*0.5*10/ln(2)*60 = 8656.2
p_max = 216.4 = alpha + alpha0
alpha = 216.2
These corrections seem to give more sensible results. The protein numbers are still the same, but the mRNA numbers are only about 1/15th of the proteins.</rdf:value>
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The original published equations were scaled and modified with reference to the same model on the Biomodels database.</rdf:value>
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