Team:BIOTEC Dresden/Project v2
From 2009.igem.org
(New page: {{:Team:BIOTEC_Dresden/NewTemplate}} === Temporal and spatial control of protein synthesis by in vitro recombination inside picoliter reactors === Manufacturing functionalized proteins ...) |
|||
Line 1: | Line 1: | ||
{{:Team:BIOTEC_Dresden/NewTemplate}} | {{:Team:BIOTEC_Dresden/NewTemplate}} | ||
- | + | ||
- | recombination inside picoliter reactors | + | |
+ | == Temporal and spatial control of protein synthesis by in vitro | ||
+ | recombination inside picoliter reactors == | ||
Manufacturing functionalized proteins in vitro poses a challenge, as | Manufacturing functionalized proteins in vitro poses a challenge, as |
Revision as of 19:12, 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.