Team:Imperial College London

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This is a template page. READ THESE INSTRUCTIONS.
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For iGEM 2009 the Imperial College London team present you with <b><i>The E.ncapsulator</i></b>; a versatile manufacturing and delivery platform by which therapeutics can be reliably targeted to the intestine.  
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Our <i>E.coli</i> chassis progresses through a series of defined stages culminating in the production of a safe, inanimate pill. This sequential process involves drug production, protective encapsulation and genome deletion. The temporal transition between each of these stages is controlled by physical and chemical methods, showing a clear engineering approach to tackle this problem.
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You are provided with this team page template with which to start the iGEM season. You may choose to personalize it to fit your team but keep the same "look." Or you may choose to take your team wiki to a different level and design your own wiki.  You can find some examples <a href="https://2009.igem.org/Help:Template/Examples">HERE</a>.
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<b><i>The E.ncapsulator</i></b> provides an innovative method to deliver any biologically synthesisable compound and bypasses the need for expensive storage, packaging and purification processes. <b><i>The E.ncapsulator</i></b> is an attractive candidate for commercial pill development and demonstrates the massive manufacturing potential in Synthetic Biology.
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<table border="0"><tr><center><b>Pushed for time? Browse through the main pages using our thumbs below.   Else, take our tour by clicking on these arrows or using the links at the top right of the page</b></center></tr>
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<tr><td width="20%"><center><a href="https://2009.igem.org/Team:Imperial_College_London/Major_results"><img style="vertical-align:bottom;" width="100%" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Homepageimage2.png"><br><b>Major Results</b></a></center></td>
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<td width="20%"><center><a href="https://2009.igem.org/Team:Imperial_College_London/Wetlab/BioBricks"><img style="vertical-align:bottom;" width="100%" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Homepageimage3.png"><br><b>Submitted Parts</b></a></center></td>
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<td width="20%" style="border-right:1px solid #000;"><center><a href="https://2009.igem.org/Team:Imperial_College_London/Achievements"><img style="vertical-align:bottom;" width="100%" src="http://i691.photobucket.com/albums/vv271/dk806/II09_Homepageimage4.png"><br><b>Achievements</b></a></center></td>
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==Creating ‘The E.ncapsulator’: in situ manufacture and oral delivery of human biopharmaceuticals==
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This year the Imperial College iGEM team project involves developing an innovative, self-contained drug fabrication and delivery system. We have focused on designing and engineering a number of modules for implementation in Escherichia coli to allow the manufacture of important biopharmaceuticals and the creation of E.ncapsulator tablets for oral delivery and release of protein-based drugs to the small intestine.<br>
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Our innovative approach incorporates a number of re-usable modular features including protein drug production, self-encapsulation and genomic neutralisation. Utilising the Escherichia coli bacterium, we are creating a re-usable chassis that will allow the development of a range of biopharmaceuticals to be delivered to the gut.  The E.ncapsulator provides an elegant solution to a range of human ailments and conditions which cannot currently be successfully treated by oral drugs.<br>
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The first module involves engineering E. coli to synthesise the protein drug of interest to a tuneable threshold. Once accomplished, activation of module two initiates the encapsulation phase, in which E. coli coats itself in a protective layer of colanic acid to form The E.ncapsulator. This protective capsule shields the biopharmaceutical against the harsh acidic environment of the stomach. The third module, genomic neutralisation, is composed of a ‘suicide trigger’ mechanism that destroys the genetic material of the bacteria. Finally, once in the small intestine, the capsule will be degraded releasing the designed biopharmaceutical to the gut micro biota where it can carry out its intended function.<br>
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The self-encapsulation of a synthetic biology chassis is new to iGEM and represents a completely novel and innovative approach to biopharmaceutical design, manufacture and delivery. Throughout the project we have followed an engineering approach that incorporates modular design, detailed modelling and simulation and systematic integration. Using such an approach has led to The E.ncapsulator coming soon to a Pharmacy near you!
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Latest revision as of 02:34, 22 October 2009

The E.ncapsulator text

The E.ncapsulator

For iGEM 2009 the Imperial College London team present you with The E.ncapsulator; a versatile manufacturing and delivery platform by which therapeutics can be reliably targeted to the intestine.
Our E.coli chassis progresses through a series of defined stages culminating in the production of a safe, inanimate pill. This sequential process involves drug production, protective encapsulation and genome deletion. The temporal transition between each of these stages is controlled by physical and chemical methods, showing a clear engineering approach to tackle this problem.

The E.ncapsulator provides an innovative method to deliver any biologically synthesisable compound and bypasses the need for expensive storage, packaging and purification processes. The E.ncapsulator is an attractive candidate for commercial pill development and demonstrates the massive manufacturing potential in Synthetic Biology.

Growth
Growth
The cells are grown to a critical cell density, before the system is started. It allows the culture to reach a sufficient cell number before the the cells are triggered to begin protein production. This is because protein production can slow cell growth.
Module 1: Protein Production
Module 1: Protein Production
The first module is induced with IPTG, which triggers the production of the protein of interest. As part of this project we have looked into two proteins and a peptide of interest.
Module 2: Encapsulation
Module 2: Encapsulation
The second module is where the cell, after having produced the peptide of interest, produces colanic acid. This creates a protecting layer around teh bacterium to shelter it from the acidity of the stomach.
Module 3: Genome deletion
Module 3: Genome deletion
Module 3 occurs after encapsulation of the cell containing the produced peptide of interest. This module makes the bacterium non-viable. It does so by over-expressing restriction enzymes which subsequently cleave the genomic DNA into small fragments. The cell is thus unable to produce any proteins and therefore unable to survive.
Secondary Encapsulation
Secondary Encapsulation
Several manufacturing considerations regarding the post-processing of the culture have been investigated. Post-processing of the culture allows the polypeptide filled cells to be converted into a pharmaceutical tablet, that can be taken orally.
Chemoinduction
Module Integration: Chemoinduction
Module 1 is induced by the addition of a compound, IPTG. This allows the user to 'kickstart' the system once the culture has reached a sufficiently high cell density.
Autoinduction
Module Integration: Autoinduction
Module 2 is triggered by a switch from glucose consumption to a secondary carbon source consumption. When the initial preferential carbon source (glucose) is exhausted, the system will metabolise the secondary carbon source that is available. This switch triggers the promoter that controls the start of Module 2. By knowing the initial concentrations of each carbon source, this acts as a programmable time delay system for the activation of encapsulation.
Thermoinduction
Module Integration: Thermoinduction
Module 3 is initiated upon an increase in temperature. The system is initially grown at 28°C, at which point Module 3 is repressed. When the temperature is raised to 42°C, this repression is blocked, triggering the start of Module 3. This temperature sensitive system was chosen as after encapsulation, chemical induction may be less effective due to limited diffusion.


Pushed for time? Browse through the main pages using our thumbs below. Else, take our tour by clicking on these arrows or using the links at the top right of the page

Major Results

Submitted Parts

Achievements
Mr. Gene   Geneart   Clontech   Giant Microbes

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