Team:TU-Delft/ProjectOverview

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<p align="justify">Methicillin-Resistant Staphylococcus aureus is causing major problems in hospitals and nursing homes. In 2002 it caused over 0.5 million infections in the United States alone, putting patients with open wounds and weakened immune systems at great risks. It is so problematic because it is very difficult to treat; these bacteria have developed resistance against almost all antibiotics available. Several newly discovered strains of MRSA even show antibiotic resistance to vancomycin and teicoplanin, which where one of the last antibiotics useful against MRSA. Although a lot of research is done on alternative treatments, not much success has been booked yet. One of the more promising methods though, seems to be by the use of antimicrobial peptides.  </p>
<p align="justify">Methicillin-Resistant Staphylococcus aureus is causing major problems in hospitals and nursing homes. In 2002 it caused over 0.5 million infections in the United States alone, putting patients with open wounds and weakened immune systems at great risks. It is so problematic because it is very difficult to treat; these bacteria have developed resistance against almost all antibiotics available. Several newly discovered strains of MRSA even show antibiotic resistance to vancomycin and teicoplanin, which where one of the last antibiotics useful against MRSA. Although a lot of research is done on alternative treatments, not much success has been booked yet. One of the more promising methods though, seems to be by the use of antimicrobial peptides.  </p>

Revision as of 21:59, 3 October 2013


Methicillin-Resistant Staphylococcus aureus is causing major problems in hospitals and nursing homes. In 2002 it caused over 0.5 million infections in the United States alone, putting patients with open wounds and weakened immune systems at great risks. It is so problematic because it is very difficult to treat; these bacteria have developed resistance against almost all antibiotics available. Several newly discovered strains of MRSA even show antibiotic resistance to vancomycin and teicoplanin, which where one of the last antibiotics useful against MRSA. Although a lot of research is done on alternative treatments, not much success has been booked yet. One of the more promising methods though, seems to be by the use of antimicrobial peptides.

Therefore, our project focusses on designing an E. coli that can detect MRSA in order to locally produce and deliver antimicrobial peptides against gram-positive bacteria. Our E. coli will detect S. aureus by its own quorum sensing system, and at that moment inactivated antimicrobial peptide is started to be produced. With the use of a timer the peptide will be activated by cleaving of an inactivating tag. With the use of the timer, high concentrations of peptide can be delivered very locally in order to efficiently kill MRSA. In order to ensure the safety of the system, the peptide-activating protease is combined with a kill switch that will kill our E. coli (Figure 1).

This project is novel because we aim to fight a life threatening, hard to cure disease by incorporating and combining components of multiple kingdoms into one organism. We let a Gram-negative bacterium sense the communication molecules of gram-positive bacteria and respond to this with an animal innate immune response. The protease activation of the antimicrobial peptide is from fungal origin.


Figure 1: Schematic diagram of the Peptidor system


The complete system is split up into different modules, all being different bio are used as building blocks.The building blocks are:

Sensing Device:Quorum Sensing System of S. aureus is engineered to our Peptidor in order to detect the presence of S. aureus Peptide Production: After the S. aureus has been detected, the mechanism of the peptide production is activated. The


Peptide Characterization
Timer: A timer was added to circuit in order the peptide pro for two main reasons. First of all the existence of the timer gives the time for the peptide to build up in the cell non-toxically before activation through cleavage
Kill Switch :