- Author:
- pmr2.import <nobody@models.cellml.org>
- Date:
- 2009-06-17 14:32:55+12:00
- Desc:
- committing version01 of heyd_drew_2003
- Permanent Source URI:
- https://models.cellml.org/workspace/heyd_drew_2003/rawfile/1474a8fafe8ae97686b4cef3987d479059d995ee/heyd_drew_2003.cellml
<?xml version='1.0' encoding='utf-8'?>
<!-- FILE : heyd_model_2003.xml
CREATED : 25th November 2003
LAST MODIFIED : 25th November 2003
AUTHOR : Catherine Lloyd
Bioengineering Institute
The University of Auckland
MODEL STATUS : This model conforms to the CellML 1.0 Specification released on
10th August 2001, and the 16/1/02 CellML Metadata 1.0 Specification.
DESCRIPTION : This file contains a CellML description of Heyd and Drew's mathematical model for elongation of a peptide chain.
CHANGES:
--><model xmlns="http://www.cellml.org/cellml/1.0#" xmlns:cmeta="http://www.cellml.org/metadata/1.0#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:bqs="http://www.cellml.org/bqs/1.0#" xmlns:cellml="http://www.cellml.org/cellml/1.0#" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:vCard="http://www.w3.org/2001/vcard-rdf/3.0#" cmeta:id="heyd_drew_2003_version01" name="heyd_drew_2003_version01">
<documentation xmlns="http://cellml.org/tmp-documentation">
<article>
<articleinfo>
<title>A Mathematical Model for the Elongation of a Peptide Chain</title>
<author>
<firstname>Catherine</firstname>
<surname>Lloyd</surname>
<affiliation>
<shortaffil>Bioengineering Institute, University of Auckland</shortaffil>
</affiliation>
</author>
</articleinfo>
<section id="sec_status">
<title>Model Status</title>
<para>
This is the original unchecked version of the model imported from the previous
CellML model repository, 24-Jan-2006.
</para>
</section>
<sect1 id="sec_structure">
<title>Model Structure</title>
<para>
Protein expression is an essential feature of cellular development and operation. The process involves the transcription of genes (DNA) into messenger RNA (mRNA) molecules, which are then translated into polypeptide chains, and finally folded and chemically modified to become functioning protein molecules. Transcription and translation are highly regulated processes, with activator, inhibitor and catalyst molecules controlling the rates of the reactions.
</para>
<para>
In 2001 Donald Drew published a mathematical model consisting of differential equations representing the rate of change in the concentration of each protein involved in polypeptide synthesis. The model also has the ability to account for the activating or inhibiting effects of transcription factors on the rate of gene transcription. This model describes each reaction in terms of kinetic rate constants for sub-parts of the overall reaction. One sub-process is peptide chain elongation which occurs during the translation of mRNA into a polypeptide. The process of elongation occurs as amino acids are added to the growing chain, one by one, facilitated by the ribosome which holds the mRNA molecule in the correct position, and the transfer RNA (tRNA) molecules which bring in the complementary amino acids. The binding of an aminoacyl-tRNA (amino acid bound tRNA complex - aa-tRNA) to the complementary site on a ribosome is catalysed by the elongation factor Tu complex (EF-Tu). EF-Tu, aa-tRNA and GTP bind together in a multi step process to form a stable ternary complex which then binds to the ribosome.
</para>
<para>
In the 2003 publication described here in CellML (see <xref linkend="sec_download_this_model"/> below), Heyd and Drew developed a mathematical model of the operation of the ribosome during peptide elongation. In addition, the reset sb-process for the elongation process is modelled (see <xref linkend="fig_reaction_diagram"/> below). They found that the rate of peptide elongation is a function of the concentration of the amino acid to be bound and the concentration of all the other amino acids. In addition, the overall elongation rate depends on the concentration of elongation factors.
</para>
<para>
The complete original paper reference is cited below:
</para>
<para>
<ulink url="http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WC7-49KH38N-1&_user=140507&_coverDate=11%2F30%2F2003&_alid=130093239&_rdoc=1&_fmt=summary&_orig=search&_qd=1&_cdi=6731&_sort=d&_docanchor=&view=c&_acct=C000011498&_version=1&_urlVersion=0&_userid=140507&md5=8c29ae12d3e6d1d991734eb86a09a834">A Mathematical Model for Elongation of a Peptide Chain</ulink>, Andrew Heyd and Donald A. Drew, 2003, <ulink url="http://www.sciencedirect.com/science?_ob=JournalURL&_cdi=6731&_auth=y&_acct=C000011498&_version=1&_urlVersion=0&_userid=140507&md5=2670d6bf58ba6625cf8c13344d6a4cb5">
<emphasis>Bulletin of Mathematical Biology</emphasis>
</ulink>, 65, 1095-1109. (<ulink url="http://www.sciencedirect.com/science?_ob=ArticleURL&_udi=B6WC7-49KH38N-1&_coverDate=11%2F30%2F2003&_alid=130093239&_rdoc=1&_fmt=&_orig=search&_qd=1&_cdi=6731&_sort=d&view=c&_acct=C000011498&_version=1&_urlVersion=0&_userid=140507&md5=40fff0ad267ad88e7678b0a02ca1bb42">Full text (HTML)</ulink> and PDF versions of the article are available on the <emphasis>Bulletin of Mathematical Biology</emphasis> website.) <ulink url="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=14607290&dopt=Abstract">PubMed ID: 14607290</ulink>
</para>
<informalfigure float="0" id="fig_reaction_diagram">
<mediaobject>
<imageobject>
<objectinfo>
<title>reaction diagram</title>
</objectinfo>
<imagedata fileref="heyd_2003.png"/>
</imageobject>
</mediaobject>
<caption>The following variables are the various states that were accounted for in the multi-step model:
A - EF-Tu:aa-tRNA complex. A1 refers to the correct complex, A2 is the wrong complex.
B - open A-site on ribosome (ribosome is able to any amino acid).
C - initial binding.
D - codon recognition.
E - GTPase activation and GTP hydrolysis.
F - EF_tu released after EF-Tu conformation change.
G - accommodation and peptide transfer.
The sub-states in the sub-process of G resetting are:
G' - ribosome after peptide transfer.
H - EF-G.
I - binding of EF-G.
J - GTP hydrolysed.
K - conformation change inducing transition state.
L - tRNA and mRNA movement.
M - ribosome returns to ground state.
B - EF-G (GDP) and tRNA dissociate, ribosome is completely reset with an open A-site.</caption>
</informalfigure>
</sect1>
</article>
</documentation>
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Heyd and Drew's mathematical model for elongation of a peptide chain.
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<vCard:FN>Catherine Lloyd</vCard:FN>
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<rdf:Description rdf:about="rdf:#df652e95-010e-4e89-afa7-c5732a4a3c98">
<dcterms:W3CDTF>2003-11-25</dcterms:W3CDTF>
</rdf:Description>
<rdf:Description rdf:about="rdf:#cda07caf-6f6b-46e8-91a2-40d9a721fa88">
<dc:creator rdf:resource="rdf:#71421e76-03cb-4abd-a3aa-aff76280c076"/>
<rdf:value>
This is the CellML description of Heyd and Drew's mathematical model
for elongation of a peptide chain.
</rdf:value>
</rdf:Description>
<rdf:Description rdf:about="rdf:#47a7851f-b46c-40ac-a0cf-fceb7560c616">
<vCard:Orgname>The University of Auckland</vCard:Orgname>
<vCard:Orgunit>The Bioengineering Institute</vCard:Orgunit>
</rdf:Description>
<rdf:Description rdf:about="rdf:#f14f9bc4-2cde-4519-843b-b741279dee3d">
<dc:creator rdf:resource="rdf:#4b99e5ca-469c-4922-bda2-d78750bd9f99"/>
<dc:title>
A Mathematical Model for Elongation of a Peptide Chain
</dc:title>
<bqs:volume>65</bqs:volume>
<bqs:first_page>1095</bqs:first_page>
<bqs:Journal rdf:resource="rdf:#4a56771d-f6b5-4ac3-ae21-8b3a52d83d42"/>
<dcterms:issued rdf:resource="rdf:#977fca24-c609-4153-b5f0-b663780362ad"/>
<bqs:last_page>1109</bqs:last_page>
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<rdf:Description rdf:about="rdf:#5af25911-a3e1-419e-921d-b084361c30aa">
<vCard:Given>Donald</vCard:Given>
<vCard:Family>Drew</vCard:Family>
<vCard:Other>A</vCard:Other>
</rdf:Description>
<rdf:Description rdf:about="rdf:#4a56771d-f6b5-4ac3-ae21-8b3a52d83d42">
<dc:title>Bulletin of Mathematical Biology</dc:title>
</rdf:Description>
<rdf:Description rdf:about="">
<dc:publisher>
The University of Auckland, Bioengineering Institute
</dc:publisher>
<dcterms:created rdf:resource="rdf:#df652e95-010e-4e89-afa7-c5732a4a3c98"/>
<dc:creator rdf:resource="rdf:#8fc2041e-592f-4b04-898d-95e0e2b0c40e"/>
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</model>
