Difference between revisions of "Team:Uppsala"

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                                     <p>The second approach used a technique called “Phage Display”, which utilizes a random peptide library expressed on the surface of phages. By repeated rounds of affinity screening, only phages with high affinity to the molecule of interest will be selected. Sequencing the genetic information of these phages has allowed us to construct multiple peptide suggestions that may bind to our nematodes’ surface proteins.  This would allow the biosensor to aggregate at the detection sites and create a stronger signal. <br><br>
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                                     <p>The second approach used a technique called “Phage Display”, which utilizes a random peptide library expressed on the surface of phages. By repeated rounds of affinity screening, only phages with high affinity to the molecule of interest will be selected. Sequencing the genetic information of these phages has allowed us to construct multiple candidate peptides that may bind to our nematodes’ surface proteins.  This would allow the biosensor to aggregate at the detection sites and create a stronger signal. <br><br>
 
                                     In our project, phage display has been used in a whole new way. Performing phage display on a whole organism is an unconventional and unpublished procedure. By creating a working protocol for the purpose of finding a specific binder for strongyles we have applied this Nobel-prize winning method in a new way.</p>
 
                                     In our project, phage display has been used in a whole new way. Performing phage display on a whole organism is an unconventional and unpublished procedure. By creating a working protocol for the purpose of finding a specific binder for strongyles we have applied this Nobel-prize winning method in a new way.</p>
 
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Revision as of 02:49, 18 October 2018





Uppsala iGEM 2018