Team:Imperial College London/Project Overview

From 2009.igem.org

Revision as of 19:29, 20 October 2009 by Tywang (Talk | contribs)

Contents

The Problem

The inspiration behind The E.ncapsulator was the inherent difficulty in delivering protein pharmaceuticals to the gut. Due to the delicate nature of proteins and the highly acidic environment present in the stomach, protein molecules are readily broken down - making oral drug delivery of protein pharmaceuticals very difficult .
There are several diseases that are treated using oral delivery of peptides. Among these are: Malnutrition (world hunger) and Phenylketonuria (PKU), a disease associated with mental retardation due to insufficient ability to metabolise phenylalanine.

II09 enzyme.png

In this project, one of our applications is on synthesising phenylalanine hydroxylase (PAH), an enzyme responsible for metabolism of phenylalanine in PKU patients. Furthermore, we propose to synthesise cellulase and deliver it as a possible solution to malnutrition.The E.ncapsulator system is a generic drug production and delivery platform. This means that potentially, we are capable of solving any problem that tackles the delivery of polypeptides to the small intestine.

Some statistics

In the table below we have provided some statistics of disorders requiring administration of polypeptide drugs. These are 2 examples out of many more, such as diabetes mellitus [1] or hemophilia [2], highlighting the need for a cost-effective and implementable solution, which is what we are offering with The E.ncapsulator.

Malnutrition (from [3]) PKU (from [4-5]])
854 million people worldwide are suffering from malnutrition (12.6% of the world population) 1 per 10,000 - 15,000 newborns are diagnosed with phenylketonuria in the USA
820 million are in developing countries It occurs with a frequency of between 1 in 4.500 (Turkey and Ireland) and 1 in 10.000 in most of Europe although in Finland the frequency is lower at 1 in 40.000 new born babies.


Our Solution

The E.ncapsulator is a novel protein manufacture and delivery platform designed to overcome these difficulties. In order to learn more about each module of the system and what its doing, hover over the different parts of the image below:

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.



Project specifications

  • Synthesis: The system is generic and potentially able to manufacture any type of polypeptide.
  • Purification: In The E.ncapsulator, polypeptide synthesis (Module 1) and encapsulation of the cells(Module 2) occur in the same place. This dual production and delivery platform means that there is no need for expensive downstream purification processes.
  • Storage: Freeze drying in the encapsulation phase and secondary encapsulation allow for storage of The E.ncapsulator.
  • Quality Control: If one cell fails to produce the polypeptide of interest, it will have minimal impact on the whole system. In that if one cell fails to produce any protein it will have a minimal impact on the whole system.
  • Safety: In order to reduce risks associated with our product, we have chosen a GRAS (generally recognised as safe) chassis. Furthermore, all the genetic material is destroyed prior ingestion to prevent any risks of horizontal gene transfer after colonisation by the bacteria.






These links may be useful to browse our results and achievements:

Major Results
Submitted Parts
Achievements
Pill Manufacture
Genealogy
 




References

[1] Diabetes Mellitus statistics
[2] Hemophilia statistics
[3] World Hunger statistics
[4] Phenylketonuria in the USA
[5] ESPKU (European statistics)
[6] More PKU statistics (browse per country)
[7] Michaelis-Menten kinetics

Mr. Gene   Geneart   Clontech   Giant Microbes