Team:UCL London/Project Description

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=Project Hypoxon=
=Project Hypoxon=
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[[Image:UCL-LabTeam.JPG||380px|right]]
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Synthetic biology is now in a position to overcome many, hitherto, cumbersome and resource consuming manufacturing tasks. Society has now accepted the advent of such entities as recombinant insulin , monoclonal antibodies etc as essential for the future well being of human life. We can now use the bio engineered tools available to us to create systems which make manufacturing health or environmentally associated products simpler and more economical.
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UCL’s Biochemical Engineering department has been at the forefront of biopharmaceutical manufacture for many years. Extraordinary advances in the life sciences have great potential to improve our quality of life through better medicines and a cleaner environment.
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Our project aims to create “independent” cells, capable of self-induction into the production phase, without the introduction of any chemical into the closed system. By exploiting genetically modified ''E.coli'' to respond to hypoxia, we eliminate the need of IPTG induction. The functioning genetic circuit would be signaled by the production of  red fluorescent proteins (RFPs).
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While the RFP can be used as a live monitoring technique for oxygen, replacing the RFP with pharmaceutical proteins promises higher yields and more consistent batches which is a step closer to providing cheaper healthcare to everyone.
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To this end, this project addresses the hypothesis that we can use auto-induction as a means of control of production of recombinant products at a pre-destined time in large production vessels thus alleviating the need for extra resources. To illustrate this we are using E.coli as our main vehicle with the prospect of removing the need for IPTG induction as a mechanism for the production of a vast array of biopharmaceuticals. We expect this technology to be equally applicable to other systems such as yeast and mammalian cells.
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==Application in Industry==
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Cells need constant monitoring for an "oxygen spike". This spike occurs when cells have reached their maximum growth capacity in the fermenter, and are competing for nutrients in the fermenter. At that point, an operator has to introduce a pre-determined volume of IPTG (chemical) into the fermenter to stop the cell growth and channel the energy into transcription of a certain gene. This is how the cells are manipulated to produce pharmaceuticals!
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It is estimated that through this auto-induction the production of economically viable biopharmaceuticals with less side-effects can be achieved. The application of this project goes further into exploring the potential of applying this principle in yeast, mammalian or other expression systems for the production of complex biomolecules for the treatment of major diseases.
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'''Reliability'''
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[[Image:Bacteria-growth.jpg||400px|left]]
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==Project Description==
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Cells go through different phases before reaching their maximum number. There is no way of telling how long the lag phase would be, or when the oxygen spike would occur. (We experienced a four day lag phase in one of our four fermentations where the cells were not dead, but not growing! This can get frustrating, and can give  ''Steve, the guardian of the fermenters'' horrible ideas like killing the cells and starting again!
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[[Image:UCL-SAHPES22.png|500px|center]]
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What if the oxygen spike happens on a weekend, or falls somewhere outside the 8-hour-shift?
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This is where auto-induction becomes useful. The cells would automatically realise the oxygen spike and change from growth to manufacturing automatically!
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During the initial phase of the fermentation process, the recombinant E.coli cells with our genetic circuit will grow very slow at first, and this initial phase is referred to as the "Log Phase". As this happens, the DOT(Dissolved Oxygen Tension) in the fermenter decreases, at a rate which is indirectly proportional to the rate of cellular growth. The DOT will continue to fall untill it falls in the region of 15-20%. Now usually during protein expression in E.coli clls lacking our genetic circuit, this is the point at which our inducer IPTG would be added manually resulting in the lacI repressser being repressed itself and thus allowing our hybrid pTAC to be expressed thus allowed the desired protein to be expressed. However, bearing in mind the DOT, we will use this unique factor to introduce hypoxia into our circuit. Essentilly, our circuit will start of with an HSP, Hypoxia Sensitive Promoter, which will detect the change in DOT when it falls belew the threshold of 20%. At that point, it will be triggered and will activate a positive feedback loop consisting of 2 promoter Activators and 2 Promoters in the following format;
 
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                                [[Image:UCL-papapa.png|150px|center]]
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'''Cost'''
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The promoter activator activates the promoter, which then activates another promoter activator and thus produces more of the promoter. This is essential as it increases the rate of protein expression. With this being activated, the VRDP, which is our red dye protein, it too will be activated subsequently resulting in  the expression of our red dye protein indicating the succesful operation of our circuit.In our circuit for the sake of proof of principle, instead of expressing a typical protein, we will introduce a genetic sequence which translates a fluorescent red protein so that once it is translated, it will secrete the red dye and hence prove that our circuit does in actual fact work and added an artistic touch to our project.
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Not only does auto-induction save money on IPTG, it can eliminate the need of IPTG storage saving massive amounts of money on refrigeration in a sterile environment(IPTG must be stored at -20 degrees). Also, there is no more risks of contamination of the IPTG, or of the batch when introducing the IPTG!
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That means that less batches are wasted, and there is therefore a lower chance of batch failure per year. Therefore, with more batches produced per annum, the cost of the drug would decrease giving more people access to it!
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The pTAC here no longer serves the purpose of being our expression system, it now serves the purpose of commencing the switch off of our circuit. This will happen by addition of IPTG which will result in the pTAC no longer being repressed. This will allow the activation of the pTAC which will activate the consecutive antiPA gene resulting in repression of the promoter activators and hence the switching off of our genetic circuit. Now in biopharmaceutical production, this extra sequence consisting of the pTAC and the antiPA is not required since there is no need to switch the genetic circuit of and so will allow maximum protein expression. But in this project, we feel it is essential to provide a mechanism for its closure, a genuine rule of thumb in Synthetic biology.
+
'''Environmental'''
 +
As mentioned above, IPTG needs to be stored at -20 degrees. Not using IPTG would eliminate the need for refrigerators, making the pharmaceutical industry a little greener.
 +
==Project Description==
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[[Image:UCL-DarreDiagProc.png|500px|center]]
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[[Image:UCL-SAHPES222.png|500px|center]]
 +
During the initial phase of the fermentation process, the recombinant ''E.coli'' cells with our genetic circuit will grow very slow at first, and this initial phase is referred to as the "Log Phase". As this happens, the DOT(Dissolved Oxygen Tension) in the fermenter decreases, at a rate which is indirectly proportional to the rate of cellular growth. The DOT will continue to fall untill it falls in the region of 15-20%. Usually during protein expression in ''E.coli'' cells lacking our genetic circuit, this is the point at which our inducer IPTG would be added, manually resulting in the LacI repressser being repressed itself and thus allowing our hybrid pTAC to be expressed. The desired protein is then expressed. However, bearing in mind the DOT, we will use this unique factor to introduce hypoxia into our circuit. Essentilly, our circuit will start of with an HSP, Hypoxia Sensitive Promoter, which will detect the change in DOT when it falls below the threshold of 20%. At that point, it will be triggered and will activate a positive feedback loop consisting of 2 promoter Activators and 2 Promoters in the following format;
 +
                                [[Image:UCL-papapa.png|150px|center]]
 +
The promoter activator activates the promoter, which then activates another promoter activator and thus produces more of the promoter. This is essential as it increases the rate of protein expression. With this being activated, the RFP, which is our red dye protein,  will be activated subsequently resulting in  the expression of our red dye protein indicating the succesful operation of our circuit. In our circuit for the sake of proof of principle, instead of expressing a typical protein, we will introduce a genetic sequence which translates a fluorescent red protein so that once it is translated, it will secrete the red dye and hence prove that our circuit does in actual fact work and added an artistic touch to our project.
 +
[[Image:Ucl-PAPAP-A.png|700px|center]]
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[[Image:UCL-Graphdarren.png|700px|centre]]
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The above diagram clearly demonstrates the effect the PA-P-PA-P loop has on the production of the promoter. Line A is that of the PA-P system alone and it takes more time, nearly double that of the  feedback loop, to transcribe the same amount of the promoter.
 +
The pTAC here no longer serves the purpose of being our expression system, it now serves the purpose of commencing the switch off of our circuit. This will happen by addition of IPTG which will result in the pTAC no longer being repressed. This will allow the activation of the pTAC which will activate the consecutive antiPA gene resulting in repression of the promoter activators and hence the switching off of our genetic circuit. Now in biopharmaceutical production, this extra sequence consisting of the pTAC and the antiPA is not required since there is no need to switch the genetic circuit of and so will allow maximum protein expression. But in this project, we feel it is essential to provide a mechanism for its closure, a genuine rule of thumb in Synthetic biology.
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[[Image:UCL-DarreDiagProc.png|500px|center]]
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Thanks to the efforts of our artists, we managed to summarize what we hoped to achieve in the lab in a simple and animation;
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<object width="920" height="785""><param name="movie" value="http://www.youtube.com/v/bmgbL9Q0_hQ?fs=1&amp;hl=en_US&amp;color1=0x234900&amp;color2=0x4e9e00"></param><param name="allowFullScreen" value="true"></param><param name="allowscriptaccess" value="always"></param><embed src="http://www.youtube.com/v/bmgbL9Q0_hQ?fs=1&amp;hl=en_US&amp;color1=0x234900&amp;color2=0x4e9e00" type="application/x-shockwave-flash" allowscriptaccess="always" allowfullscreen="true" width="920" height="785"></embed></object>
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</html>
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Here, the '''green''' blocks represent the level  of DOT in the fermenter, '''red-blue''' being the rate of protein expression subsequent ( 2 representing the positive feedback loop of 2 promoters and 2 promoter activators), and '''yellow''' being the activation of the hypoxia sensitive promoter due to the reduction of the DOT level below the threshold of around 20%.
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You can see in the animation that initially, there is a slow then rapid fall in the DOT concentration, as it falls to very low levels, hypoxia is activated shown by the sudden appearance then disappearance of the yellow lego bricks. At that time, the rate of protein expression increases as our genetic circuit is now active. A subsequent increase in DOT levels is also observed. These set of rapid changes in DOT levels is known as "The DOT Spyke", and takes place as the fermentation process changes from one in batch to fed-batch due to the consequent addition of glycerol to maintain the cells during protein expression.
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<div class='clearfix'> </div>
 
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Latest revision as of 02:17, 28 October 2010

UCL IGEM 2010

RETURN TO IGEM 2010

Project Hypoxon

Project Abstract

UCL-LabTeam.JPG

UCL’s Biochemical Engineering department has been at the forefront of biopharmaceutical manufacture for many years. Extraordinary advances in the life sciences have great potential to improve our quality of life through better medicines and a cleaner environment.

Our project aims to create “independent” cells, capable of self-induction into the production phase, without the introduction of any chemical into the closed system. By exploiting genetically modified E.coli to respond to hypoxia, we eliminate the need of IPTG induction. The functioning genetic circuit would be signaled by the production of red fluorescent proteins (RFPs).

While the RFP can be used as a live monitoring technique for oxygen, replacing the RFP with pharmaceutical proteins promises higher yields and more consistent batches which is a step closer to providing cheaper healthcare to everyone.

Application in Industry

Cells need constant monitoring for an "oxygen spike". This spike occurs when cells have reached their maximum growth capacity in the fermenter, and are competing for nutrients in the fermenter. At that point, an operator has to introduce a pre-determined volume of IPTG (chemical) into the fermenter to stop the cell growth and channel the energy into transcription of a certain gene. This is how the cells are manipulated to produce pharmaceuticals!

Reliability

Bacteria-growth.jpg

Cells go through different phases before reaching their maximum number. There is no way of telling how long the lag phase would be, or when the oxygen spike would occur. (We experienced a four day lag phase in one of our four fermentations where the cells were not dead, but not growing! This can get frustrating, and can give Steve, the guardian of the fermenters horrible ideas like killing the cells and starting again!

What if the oxygen spike happens on a weekend, or falls somewhere outside the 8-hour-shift? This is where auto-induction becomes useful. The cells would automatically realise the oxygen spike and change from growth to manufacturing automatically!


Cost

Not only does auto-induction save money on IPTG, it can eliminate the need of IPTG storage saving massive amounts of money on refrigeration in a sterile environment(IPTG must be stored at -20 degrees). Also, there is no more risks of contamination of the IPTG, or of the batch when introducing the IPTG! That means that less batches are wasted, and there is therefore a lower chance of batch failure per year. Therefore, with more batches produced per annum, the cost of the drug would decrease giving more people access to it!

Environmental

As mentioned above, IPTG needs to be stored at -20 degrees. Not using IPTG would eliminate the need for refrigerators, making the pharmaceutical industry a little greener.

Project Description

UCL-SAHPES222.png

During the initial phase of the fermentation process, the recombinant E.coli cells with our genetic circuit will grow very slow at first, and this initial phase is referred to as the "Log Phase". As this happens, the DOT(Dissolved Oxygen Tension) in the fermenter decreases, at a rate which is indirectly proportional to the rate of cellular growth. The DOT will continue to fall untill it falls in the region of 15-20%. Usually during protein expression in E.coli cells lacking our genetic circuit, this is the point at which our inducer IPTG would be added, manually resulting in the LacI repressser being repressed itself and thus allowing our hybrid pTAC to be expressed. The desired protein is then expressed. However, bearing in mind the DOT, we will use this unique factor to introduce hypoxia into our circuit. Essentilly, our circuit will start of with an HSP, Hypoxia Sensitive Promoter, which will detect the change in DOT when it falls below the threshold of 20%. At that point, it will be triggered and will activate a positive feedback loop consisting of 2 promoter Activators and 2 Promoters in the following format;

UCL-papapa.png

The promoter activator activates the promoter, which then activates another promoter activator and thus produces more of the promoter. This is essential as it increases the rate of protein expression. With this being activated, the RFP, which is our red dye protein, will be activated subsequently resulting in the expression of our red dye protein indicating the succesful operation of our circuit. In our circuit for the sake of proof of principle, instead of expressing a typical protein, we will introduce a genetic sequence which translates a fluorescent red protein so that once it is translated, it will secrete the red dye and hence prove that our circuit does in actual fact work and added an artistic touch to our project.

Ucl-PAPAP-A.png

The above diagram clearly demonstrates the effect the PA-P-PA-P loop has on the production of the promoter. Line A is that of the PA-P system alone and it takes more time, nearly double that of the feedback loop, to transcribe the same amount of the promoter.

The pTAC here no longer serves the purpose of being our expression system, it now serves the purpose of commencing the switch off of our circuit. This will happen by addition of IPTG which will result in the pTAC no longer being repressed. This will allow the activation of the pTAC which will activate the consecutive antiPA gene resulting in repression of the promoter activators and hence the switching off of our genetic circuit. Now in biopharmaceutical production, this extra sequence consisting of the pTAC and the antiPA is not required since there is no need to switch the genetic circuit of and so will allow maximum protein expression. But in this project, we feel it is essential to provide a mechanism for its closure, a genuine rule of thumb in Synthetic biology.


UCL-DarreDiagProc.png


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