Team:KULeuven/Model/Output

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==[https://static.igem.org/mediawiki/2008/d/d9/Output_v2.zip Output] ==
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[[Image:pictogram_output.png|120px|right]]
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== Output ==
=== Position in the system ===
=== Position in the system ===
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The output is directly linked to the input subsystem, having its input regulated by the output (OmpF) of the light sensor...
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The output system is one of three modules directly linked to the input. The output system is a simple gene regulation, of which transcription is repressed by TetR - and can be activated by anhydrotetracyclin. The output signal is GFP (green fluorescent protein).
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In the applied project of dealing with Crohn's disease this would be replaced by the drug necessary to cure the local inflammation. The drug concentration would be proportional to the amount of local inflammation sensed.
=== Describing the system ===
=== Describing the system ===
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see also: [https://2008.igem.org/Team:KULeuven/Project/Output Project:Output]
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[[Image:Output_BioBrick.jpg|center]]
==== ODE's ====
==== ODE's ====
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<html>
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<body>
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<p>
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<a href="https://static.igem.org/mediawiki/2008/6/66/OutputODE.pdf">
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<img border="0" src="https://2008.igem.org/wiki/skins/common/images/icons/fileicon-pdf.png" width="65" height="60">
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</a>
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</p>
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</body>
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</html>
==== Parameters ====
==== Parameters ====
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{| width=70% style="border: 1px solid #003E81; background-color: #EEFFFF;"
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{| width=80% style="border: 1px solid #003E81; background-color: #EEFFFF;"
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|+ ''Parameter values Output''
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|+ ''Parameter values (Output)''
|-
|-
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! width=30% | Name
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! width=15% | Name
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! width=30% | Value
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! width=15% | Value
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! width=30% | Reference
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! width=40% | Comments
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! width=10% | Reference
|-
|-
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! colspan="3" style="border-bottom: 1px solid #003E81;" | Degradation
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! colspan="4" style="border-bottom: 1px solid #003E81;" | Degradation Rates
|-
|-
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| d<sub>CFP</sub> (protein)
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| d<sub>GFP</sub>
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| 1.05E-4 s<sup>-1</sup>
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| d<sub>LVA</sub> = 2.814E-4 s<sup>-1</sup>
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| [http://parts.mit.edu/igem07/index.php/ETHZ/Parameters link]
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| LVA-tag reduces lifetime to 40 minutes
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| [https://2008.igem.org/Team:KULeuven/Model/Output#References [1<html>]</html>] [https://2008.igem.org/Team:KULeuven/Model/Output#References [4<html>]</html>]
|-
|-
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| d<sub>RNA_CFP</sub> (mRNA)
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| d<sub>mRNA_GFP</sub>
| 0.0023 s<sup>-1</sup>
| 0.0023 s<sup>-1</sup>
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| [http://www.pubmedcentral.nih.gov/picrender.fcgi?artid=124983&blobtype=pdf link]
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|
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| [https://2008.igem.org/Team:KULeuven/Model/Output#References [2<html>]</html>]
|-
|-
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! colspan="3" style="border-bottom: 1px solid #003E81;" | Transcription Rate
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! colspan="4" style="border-bottom: 1px solid #003E81;" | Transcription Rates
|-
|-
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| k1<sub>CFP</sub>
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| TetR_var_transcr_rate
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| OmpF dependent
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| p(TetR) dependent
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|
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| (GFP) between 5E-5 and 0.0125 s<sup>-1</sup> ~ [aTc]
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| [https://2008.igem.org/Team:KULeuven/Model/Output#References [3<html>]</html>]
|-
|-
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! colspan="3" style="border-bottom: 1px solid #003E81;" | Translation Rate
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! colspan="4" style="border-bottom: 1px solid #003E81;" | Translation Rates
|-
|-
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| k2<sub>CFP</sub>
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| k<sub>GFP</sub>
| 0.167 s<sup>-1</sup>
| 0.167 s<sup>-1</sup>
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| Based on efficiency RBS
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| translation rate for B0032 RBS (0.3 relative efficiency)
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| [https://2008.igem.org/Team:KULeuven/Model/Output#References [5<html>]</html>]
|}
|}
=== Models ===
=== Models ===
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==== CellDesigner ====
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==== CellDesigner ([https://static.igem.org/mediawiki/2008/5/53/Output_CellDesigner.zip SBML file]) ====
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[[Image:output_v2.png|500px|center|Output]]
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[[Image:Output_CellDesigner.png|500px|center|Output]]
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==== Matlab ([https://static.igem.org/mediawiki/2008/1/16/Output_Matlab.zip SBML file]) ====
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[[Image:Output_Matlab.jpg|center]]
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=== Simulations ===
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Several simulations were conducted. The following two show the transient respons and eventual saturation of the output system to a low (left figure) and a high (right figure) input signal (TetR = 5E-5 vs 0.0125 s<sup>-1</sup>). There is a great distinction in the number of GFP molecules between the two input signals. All graphs have amounts (number of molecules in the cell) plotted vs time, measured in seconds.
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<html>
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<div class="center">
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<div class="noborder" style="width: 1050px;">
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<img src="https://static.igem.org/mediawiki/2008/7/74/Sim_output_1.png" style="float: left; width: 450px; height: 400px; margin: 0 15px;" />
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<img src="https://static.igem.org/mediawiki/2008/3/3b/Sim_output_2.png" style="float: left; width: 450px; height: 400px; margin: 0 5px;" />
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</div></div></html>
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The next figure shows the switching behaviour of the output system to an light signal turning on and off:
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[[Image:Sim_output_3.png|450px|center]]
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=== Sensitivity Analysis ===
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[[Image:Sens output2.png|center]]
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=== References ===
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<html xmlns="http://www.w3.org/1999/xhtml" xml:lang="en">
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<head>
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<meta http-equiv="Content-Type" content="text/html; charset=utf-8"/>
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<title>Bibliography</title>
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</head>
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<body>
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<table style="border-collapse:collapse;line-height:1.1em;">
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<tr style="vertical-align:top;"><td>[1]</td><td style="padding-left:4pt;">“ETHZ/Parameters - IGEM07”; https://2007.igem.org/ETHZ/Parameters.</td></tr>
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<tr><td colspan="2">&nbsp;</td></tr>
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<tr style="vertical-align:top;"><td>[2]</td><td style="padding-left:4pt;">J.A. Bernstein et al., “Global analysis of mRNA decay and abundance in Escherichia coli at single-gene resolution using two-color fluorescent DNA microarrays,” <span style="font-style:italic;">Proceedings of the National Academy of Sciences of the United States of America</span>,  vol. 99, Jul. 2002, pp. 9697–9702. <span class="Z3988" title="url_ver=Z39.88-2004&amp;ctx_ver=Z39.88-2004&amp;rft_id=info%3Adoi/10.1073/pnas.112318199&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.atitle=Global%20analysis%20of%20mRNA%20decay%20and%20abundance%20in%20Escherichia%20coli%20at%20single-gene%20resolution%20using%20two-color%20fluorescent%20DNA%20microarrays&amp;rft.jtitle=Proceedings%20of%20the%20National%20Academy%20of%20Sciences%20of%20the%20United%20States%20of%20America&amp;rft.stitle=Proc%20Natl%20Acad%20Sci%20U%20S%20A.%20&amp;rft.volume=99&amp;rft.issue=15&amp;rft.aufirst=Jonathan%20A.&amp;rft.aulast=Bernstein&amp;rft.au=Jonathan%20A.%20Bernstein&amp;rft.au=Arkady%20B.%20Khodursky&amp;rft.au=Pei-Hsun%20Lin&amp;rft.au=Sue%20Lin-Chao&amp;rft.au=Stanley%20N.%20Cohen&amp;rft.date=2002-07-23&amp;rft.pages=9697%E2%80%939702"></span></td></tr>
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<tr><td colspan="2">&nbsp;</td></tr>
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<tr style="vertical-align:top;"><td>[3]</td><td style="padding-left:4pt;">M. Bon, S.J. McGowan, and P.R. Cook, “Many expressed genes in bacteria and yeast are transcribed only once per cell cycle,” <span style="font-style:italic;">FASEB J.</span>,  vol. 20, Aug. 2006, pp. 1721-1723. <span class="Z3988" title="url_ver=Z39.88-2004&amp;ctx_ver=Z39.88-2004&amp;rft_id=info%3Adoi/10.1096/fj.06-6087fje&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.atitle=Many%20expressed%20genes%20in%20bacteria%20and%20yeast%20are%20transcribed%20only%20once%20per%20cell%20cycle&amp;rft.jtitle=FASEB%20J.&amp;rft.volume=20&amp;rft.issue=10&amp;rft.aufirst=Michael&amp;rft.aulast=Bon&amp;rft.au=Michael%20Bon&amp;rft.au=Simon%20J.%20McGowan&amp;rft.au=Peter%20R.%20Cook&amp;rft.date=2006-08-01&amp;rft.pages=1721-1723"></span></td></tr>
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<tr><td colspan="2">&nbsp;</td></tr>
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<tr style="vertical-align:top;"><td>[4]</td><td style="padding-left:4pt;">J.B. Andersen et al., “New Unstable Variants of Green Fluorescent Protein for Studies of Transient Gene Expression in Bacteria,” <span style="font-style:italic;">Applied and Environmental Microbiology</span>,  vol. 64, Jun. 1998, pp. 2240–2246. <span class="Z3988" title="url_ver=Z39.88-2004&amp;ctx_ver=Z39.88-2004&amp;rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&amp;rft.genre=article&amp;rft.atitle=New%20Unstable%20Variants%20of%20Green%20Fluorescent%20Protein%20for%20Studies%20of%20Transient%20Gene%20Expression%20in%20Bacteria&amp;rft.jtitle=Applied%20and%20Environmental%20Microbiology&amp;rft.stitle=Appl%20Environ%20Microbiol.%20&amp;rft.volume=64&amp;rft.issue=6&amp;rft.aufirst=Jens%20Bo&amp;rft.aulast=Andersen&amp;rft.au=Jens%20Bo%20Andersen&amp;rft.au=Claus%20Sternberg&amp;rft.au=Lars%20Kongsbak%20Poulsen&amp;rft.au=Sara%20Petersen%20Bj%C3%B8rn&amp;rft.au=Michael%20Givskov&amp;rft.au=S%C3%B8ren%20Molin&amp;rft.date=1998-06&amp;rft.pages=2240%E2%80%932246"></span></td></tr>
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<tr><td colspan="2">&nbsp;</td></tr>
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<tr style="vertical-align:top;"><td>[5]</td><td style="padding-left:4pt;">“Part:BBa B0032 - partsregistry.org”; http://partsregistry.org/Part:BBa_B0032.</td></tr>
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<tr><td colspan="2">&nbsp;</td></tr>
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==== Matlab Symbiology ====
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</table></body>
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</html>

Latest revision as of 22:47, 29 October 2008

  dock/undock dropdown  

Pictogram output.png

Contents

Output

Position in the system

The output system is one of three modules directly linked to the input. The output system is a simple gene regulation, of which transcription is repressed by TetR - and can be activated by anhydrotetracyclin. The output signal is GFP (green fluorescent protein).

In the applied project of dealing with Crohn's disease this would be replaced by the drug necessary to cure the local inflammation. The drug concentration would be proportional to the amount of local inflammation sensed.

Describing the system

see also: Project:Output

Output BioBrick.jpg

ODE's

Parameters

Parameter values (Output)
Name Value Comments Reference
Degradation Rates
dGFP dLVA = 2.814E-4 s-1 LVA-tag reduces lifetime to 40 minutes [1] [4]
dmRNA_GFP 0.0023 s-1 [2]
Transcription Rates
TetR_var_transcr_rate p(TetR) dependent (GFP) between 5E-5 and 0.0125 s-1 ~ [aTc] [3]
Translation Rates
kGFP 0.167 s-1 translation rate for B0032 RBS (0.3 relative efficiency) [5]

Models

CellDesigner (SBML file)

Output


Matlab (SBML file)

Output Matlab.jpg


Simulations

Several simulations were conducted. The following two show the transient respons and eventual saturation of the output system to a low (left figure) and a high (right figure) input signal (TetR = 5E-5 vs 0.0125 s-1). There is a great distinction in the number of GFP molecules between the two input signals. All graphs have amounts (number of molecules in the cell) plotted vs time, measured in seconds.

The next figure shows the switching behaviour of the output system to an light signal turning on and off:

Sim output 3.png

Sensitivity Analysis

Sens output2.png

References

Bibliography

[1]“ETHZ/Parameters - IGEM07”; https://2007.igem.org/ETHZ/Parameters.
 
[2]J.A. Bernstein et al., “Global analysis of mRNA decay and abundance in Escherichia coli at single-gene resolution using two-color fluorescent DNA microarrays,” Proceedings of the National Academy of Sciences of the United States of America, vol. 99, Jul. 2002, pp. 9697–9702.
 
[3]M. Bon, S.J. McGowan, and P.R. Cook, “Many expressed genes in bacteria and yeast are transcribed only once per cell cycle,” FASEB J., vol. 20, Aug. 2006, pp. 1721-1723.
 
[4]J.B. Andersen et al., “New Unstable Variants of Green Fluorescent Protein for Studies of Transient Gene Expression in Bacteria,” Applied and Environmental Microbiology, vol. 64, Jun. 1998, pp. 2240–2246.
 
[5]“Part:BBa B0032 - partsregistry.org”; http://partsregistry.org/Part:BBa_B0032.
 

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