Team:BIOTEC Dresden/Project v2

From 2009.igem.org

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recombination inside picoliter reactors  ===
recombination inside picoliter reactors  ===
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Manufacturing functionalized proteins in vitro poses a challenge, as  
+
Manufacturing functionalized proteins in vitro poses a challenge, as it requires coordinated molecular assemblies and multi-step reactions. In this project we aim to control, over time and space, the production of proteins tagged with a silver-binding peptide for in situ silver nanoparticle nucleation inside microdroplets generated by microfluidic devices. Combining a transcription-translation system with protein coding genes and a recombination logic inside microdroplets provides spatial control. Moreover, in the microfluidic chamber we can pinpoint the beginning of synthesis, and easily track and isolate the droplets. Site-specific recombination generates a molecular timer for temporal control of protein synthesis. Unlike transcriptional regulation, this method gives true all-or-none induction due to covalent modification of DNA by Flp recombinase. Determining the transfer curve of inter-FRT site distance versus average recombination time allows the onset of gene expression to be predicted. We then apply this Flp reporter system as a powerful PoPS measurement device.  
-
it requires coordinated molecular assemblies and multi-step reactions.  
+
-
In this project we aim to control, over time and space, the production  
+
-
of proteins tagged with a silver-binding peptide for in situ silver  
+
-
nanoparticle nucleation inside microdroplets generated by microfluidic  
+
-
devices. Combining a transcription-translation system with protein  
+
-
coding genes and a recombination logic inside microdroplets provides  
+
-
spatial control. Moreover, in the microfluidic chamber we can pinpoint  
+
-
the beginning of synthesis, and easily track and isolate the droplets.  
+
-
Site-specific recombination generates a molecular timer for temporal  
+
-
control of protein synthesis. Unlike transcriptional regulation, this  
+
-
method gives true all-or-none induction due to covalent modification  
+
-
of DNA by Flp recombinase. Determining the transfer curve of inter-FRT  
+
-
site distance versus average recombination time allows the onset of  
+
-
gene expression to be predicted. We then apply this Flp reporter  
+
-
system as a powerful PoPS measurement device.  
+
-
 
+
{{:Team:BIOTEC_Dresden/NewTemplateEnd}}
{{:Team:BIOTEC_Dresden/NewTemplateEnd}}

Revision as of 19:15, 19 September 2009

=== Temporal and spatial control of protein synthesis by in vitro recombination inside picoliter reactors ===

Manufacturing functionalized proteins in vitro poses a challenge, as it requires coordinated molecular assemblies and multi-step reactions. In this project we aim to control, over time and space, the production of proteins tagged with a silver-binding peptide for in situ silver nanoparticle nucleation inside microdroplets generated by microfluidic devices. Combining a transcription-translation system with protein coding genes and a recombination logic inside microdroplets provides spatial control. Moreover, in the microfluidic chamber we can pinpoint the beginning of synthesis, and easily track and isolate the droplets. Site-specific recombination generates a molecular timer for temporal control of protein synthesis. Unlike transcriptional regulation, this method gives true all-or-none induction due to covalent modification of DNA by Flp recombinase. Determining the transfer curve of inter-FRT site distance versus average recombination time allows the onset of gene expression to be predicted. We then apply this Flp reporter system as a powerful PoPS measurement device.

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