Team:BIOTEC Dresden/Project v2
From 2009.igem.org
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recombination inside picoliter reactors === | recombination inside picoliter reactors === | ||
- | 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.