Difference between revisions of "Team:Bielefeld-CeBiTec/Results"
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| − | <div><p>We constructed functional biosensors for date rape drugs, copper and mercury that work in a lyophilized in vitro transcription/translation system applied to paper. We decided to work with second cell-free | + | <div><p>We constructed functional biosensors for date rape drugs, copper and mercury that work in a lyophilized <i>in vitro</i> transcription/translation system applied to paper. Different factors were modelled to enhance the functionality of our cell-free protein synthesis and implemented successfully. We decided to work with a second cell-free approach as well, to further increase speed and durability. A functional protocol for this Plasmid Repressor Interaction Assay was established. <br> |
| + | The fluorescence output could be analyzed by our newly developed filter system with a smartphone app we programmed. <br> Along the course of our project we came across certain pieces of information, which could certainly cause damage if misused. Thus, we decided to put a great effort into the human practices aspect of our project by creating an extensive report on the topic "dual use".<br> | ||
For detailed information on our results, please click into the corresponding areas of our overview picture (noch in Arbeit). For a first short summary on the different topics stay on this page. | For detailed information on our results, please click into the corresponding areas of our overview picture (noch in Arbeit). For a first short summary on the different topics stay on this page. | ||
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Revision as of 17:19, 14 September 2015
Results
Here you can find an overview of our results.
We constructed functional biosensors for date rape drugs, copper and mercury that work in a lyophilized in vitro transcription/translation system applied to paper. Different factors were modelled to enhance the functionality of our cell-free protein synthesis and implemented successfully. We decided to work with a second cell-free approach as well, to further increase speed and durability. A functional protocol for this Plasmid Repressor Interaction Assay was established.
The fluorescence output could be analyzed by our newly developed filter system with a smartphone app we programmed.
Along the course of our project we came across certain pieces of information, which could certainly cause damage if misused. Thus, we decided to put a great effort into the human practices aspect of our project by creating an extensive report on the topic "dual use".
For detailed information on our results, please click into the corresponding areas of our overview picture (noch in Arbeit). For a first short summary on the different topics stay on this page.
We constructed biosensors for date rape drugs, copper and mercury that work in an lyophilized in vitro transcription/translation system applied to paper. We decided to work with two different cell-free systems, both were functional. Different factors were modelled to enhance to functionality of the system. The fluorescence output could be analyzed by our newly developed filter system with a simple smartphone app. Since working with date rape drugs is an ... issue, we decided to put a great effort into the human practices aspect of our project by creating a report on the topic of "dual use", in order to prevent spreading of misusable information and fathom the limits of open source ....
For detailed information on our results, please click into the corresponding areas of our overview picture. For a first short impression, keep reading this page.
We were able to establish a new assay called the plasmid repressor interaction assay (PRIA) for the model system LacI-lacO. For the implementation of the assay on paper we immobilized amino- and Cy3-labeled DNA containing the operator site successfully on filter paper. We were able to prove with an electrophoretic mobility shift assay that the repressor proteins (ArsR, LacI and BlcR) fused with sfGFP we used can bind to oligonucleotides with the corresponding operator site (arsO, lacO, Pblc). For the detection of the fusion protein and Cy3-labeled DNA we were able to exhibit fluorescence of them both with the Ettan DIGE scanner.
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