Team:EPF-Lausanne/Tools/Microfluidics

From 2011.igem.org

(Difference between revisions)
(Microfluidics in synthetic biology)
 
(13 intermediate revisions not shown)
Line 1: Line 1:
-
{{:Team:EPF-Lausanne/Templates/Header|title=Microfluidics}}
+
{{:Team:EPF-Lausanne/Templates/MicrofluidicsHeader|title=Microfluidics}}
-
To characterise our transcription factors, we used a lot of microfluidics, a tool underused by the iGEM community. We were lucky to have experts under hand to help us get started, so in turn here is our effort to promote microfluidics within the iGEM community, and help future teams use it.
+
To characterise our transcription factors, we used a lot of microfluidics, a tool underused by the iGEM community. We were lucky to have experts at hand to help us get started, so in turn here is our effort to promote microfluidics within the iGEM community, and help future teams use it.
-
'''Skip straight to:'''
+
== Microfluidics in Synthetic Biology ==
-
* [[Team:EPF-Lausanne/Tools/Microfluidics/HowTo1|The microfluidics how-to, part I]]: Making chips.
+
Microfluidics is a powerful tool for biological research, having a wide range of applications. Essentially any molecular biology technique can be adapted, including:
-
* [[Team:EPF-Lausanne/Tools/Microfluidics/HowTo2|The microfluidics how-to, part II]]: Build your own setup.
+
-
* [[Team:EPF-Lausanne/Tools/Microfluidics/Tamagotchip|Tamagotchip]]: A microfluidics game to promote microfluidics within the iGEM community.
+
-
 
+
-
== Microfluidics in synthetic biology ==
+
-
 
+
-
Microfluidics is a powerful tool for biological research, having a wide range of applications. Here is a non-exhaustive list:
+
* On-chip gene synthesis: protein expression from coding DNA
* On-chip gene synthesis: protein expression from coding DNA
-
* On-chip chemostat chambers: can be used to trace the faith of a single bacterium or to grow bacteria/yeast
+
* On-chip chemostat chambers: can be used to trace the fate of a single bacterium or to grow bacteria/yeast
-
* Protein-protein interaction screening: for example between SH3 domains or to detect antibody binding
+
* Protein-protein interaction screening
-
* DNA-protein interactions: to determine the binding affinity of a transcription factor or to discover new regulatory proteins
+
* Protein-DNA/RNA interactions: to determine the binding affinity of a transcription factor or to discover new regulatory proteins
-
These experiments share the same advantages when ported on-chip: reagent volumes are reduced, therefore minimising cost, and the tiny size of each reaction chamber allows massive parallelisation of the experiment, enabling high-throughput screening. More specifically, ''in vitro'' gene synthesis becomes affordable at this scale. Our MITOMI chip contains 768 wells, all visible in one frame, which allowed us to quantify affinity of hundreds of protein-DNA combinations in a single picture. The small channels also allow fine control over reaction conditions. Most soluble reagents can be used, including DNA, proteins, molecule libraries, and so on - allowing much creativity in experimental design.
+
[[File:EPFL-MITOMI shot.png|250px|right|thumb|A single picture gives us the binding affinity of 756 protein-DNA pairs]]
-
Few iGEM teams used this technology for their projects. We believe that promoting the use of microfluidics can help iGEM and improve the Parts Registry, specifically by providing more thorough part characterisation. To this end, we wrote a guide to get started with microfluidics, focusing on how to build a laboratory setup [[Team:EPF-Lausanne/Tools/Microfluidics/HowTo2|build a setup]] and outlining [[Team:EPF-Lausanne/Tools/Microfluidics/HowTo1|chip fabrication]]. To tickle the community's interest, we also created a [[Team:EPF-Lausanne/Tools/Microfluidics/Tamagotchip|live online microfluidics game]], where iGEMers can control a chip located in our lab from their web browser.
+
These techniques all share the same advantages when ported on-chip: reagent volumes are reduced, therefore minimising cost, and the tiny size of each reaction chamber allows massive parallelisation of the experiment, enabling high-throughput screening. More specifically, ''in vitro'' gene synthesis becomes affordable at this scale. Our MITOMI chip contains 768 wells, all visible in one frame, which allowed us to quantify the affinity of hundreds of protein-DNA combinations in a single experiment. The small channels also allow fine control over reaction conditions. Most soluble reagents can be used, including DNA, proteins, molecule libraries, and so on - allowing much creativity in experimental design.
-
[[File:EPFL-Muigi-schematic.png|600px|100%]]
+
Few iGEM teams used this technology for their projects. We believe that promoting the use of microfluidics can help iGEM and improve the Parts Registry, specifically by providing more thorough biobrick part characterisation. To this end, we wrote a guide to get started with microfluidics, focusing on how to [[Team:EPF-Lausanne/Tools/Microfluidics/HowTo2|build a setup]] and outlining [[Team:EPF-Lausanne/Tools/Microfluidics/HowTo1|chip fabrication]]. To tickle the community's interest, we also created a [[Team:EPF-Lausanne/Tools/Microfluidics/Tamagotchip|live online microfluidics game]], where iGEMers can control a chip located in our lab from their web browser.
{{:Team:EPF-Lausanne/Templates/Footer}}
{{:Team:EPF-Lausanne/Templates/Footer}}

Latest revision as of 19:52, 28 October 2011