Team:ETHZ Basel

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= Welcome to the wiki of the ETH Zurich iGEM team =
= Welcome to the wiki of the ETH Zurich iGEM team =
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iGEM 2010 ETH Zurich
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<br>Information processing on the basis of the ''E. lemming''
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<br>Inspired by the video game lemmings we want to navigate an ''E. coli'' bacterium across the perilous downs of a micro fluidic chamber. The player observes his bacterium on the screen of a microscope and directs it into any desired direction using a joystick.
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<br>Our [[Team:ETHZ_Basel/Project|project]] is divided in two important parts: creating the ''E. lemming'' and establishing controller software as an interface between player and microscope.
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<br>The ''E. lemming'' relies on a modified chemotactic pathway, which is tunable by light pulses. Mathematical models predicted the best layout of the pathway which was then implemented into ''E. coli''. To learn more about the E. lemming see the [[Team:ETHZ_Basel/Project/Molecular_mechanism|''E. lemming'']] section.
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<br>The controller software assesses the position and the direction the bacterium swims to and processes the input of the player into appropriate light pulses. To learn more about controller software please see the  [[Team:ETHZ_Basel/Project/Information_processing|Information Processing]] section.
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== E. lemming ==
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[[Image:Setup.jpg|thumb|400px|'''Setup to control E. lemming movements.''' An automatized microscope images E. lemming. A connected computer system detects and tracks the cells. The direction of movement of E. lemming is compared to the desired direction defined by the user, e.g. with a joystick. If the direction of movement deviates too much from the desired direction, the digital controller induces tumbling by sending a red light pulse. Otherwise, tumbling is repressed by sending a far-red light pulse.]]
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<h2>Project</h2>
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<small>What is E. lemming?</small>
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<p><a href="https://2010.igem.org/Team:ETHZ_Basel/Project">Click here to learn more.</a> </p>
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<a href="https://static.igem.org/mediawiki/2010/8/84/ETHZ_Basel_teaser_project.png"><img src="https://static.igem.org/mediawiki/2010/b/bd/ETHZ_Basel_teaser_project_thumb.png"></a>
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<h2>Project</h2>
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<small>What is E. lemming?</small>
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<p><a href="https://2010.igem.org/Team:ETHZ_Basel/Project">Click here to learn more.</a> </p>
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<a href="https://static.igem.org/mediawiki/2010/b/b8/ETHZ_Basel_teaser_molecular_mechanism.png"><img src="https://static.igem.org/mediawiki/2010/7/7a/ETHZ_Basel_teaser_molecular_mechanism_thumb.png"></a>
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<h2>Molecular Mechanism</h2>
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<small>How does it work?</small>
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<p><a href="https://2010.igem.org/Team:ETHZ_Basel/Project/Molecular_Mechanism">Click here to learn more.</a> </p>
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<h2>Controlling</h2>
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<small>How is it controlled?</small>
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<p><a href="https://2010.igem.org/Team:ETHZ_Basel/Project/Information_Processing">Click here to learn more.</a> </p>
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<h2>Biology & Wet Laboratory</h2>
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<small>How is it implemented?</small>
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<p><a href="https://2010.igem.org/Team:ETHZ_Basel/Biology">Click here to learn more.</a> </p>
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<a href="https://static.igem.org/mediawiki/2010/1/16/ETHZ_Basel_teaser_molecular_models.png"><img src="https://static.igem.org/mediawiki/2010/1/1f/ETHZ_Basel_teaser_molecular_models_thumb.png"></a>
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<h2>Molecular Modeling</h2>
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<small>How does modeling help?</small>
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<p><a href="https://2010.igem.org/Team:ETHZ_Basel/Modeling">Click here to learn more.</a> </p>
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<a href="https://static.igem.org/mediawiki/2010/2/21/ETHZ_Basel_teaser_information_processing.png"><img src="https://static.igem.org/mediawiki/2010/5/52/ETHZ_Basel_teaser_information_processing_thumb.png"></a>
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<h2>Information Processing</h2>
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<small>How is it controlled in detail?</small>
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<p><a href="https://2010.igem.org/Team:ETHZ_Basel/InformationProcessing">Click here to learn more.</a> </p>
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The core idea of our project is to control chemotaxis of ''E. coli'' by means of light! We'll realize this by hijacking and perturbing the tumbling / directed flagellar movement apparatus. By coupling directed flagellar movement regulating proteins to a '''novel synthetic light-sensitive spatial localization system''', their activity can be controlled reversibly. A light-sensitive dimerizing complex fused to this regulating proteins at a spatially fixed location is induced by light pulses and therefore localization of the two molecules can be manipulated.  Tumbling / directed flagellar movement rates are monitored by image processing algorithms, which are linked to the light-pulse generator. This means that ''E. coli'' tumbling is induced or suppressed simply by pressing a light switch! This synthetic network enables control of single E. coli cells: '''We'll make them move like mindless "Lemmings"''' in the direction they are forced to go!
The core idea of our project is to control chemotaxis of ''E. coli'' by means of light! We'll realize this by hijacking and perturbing the tumbling / directed flagellar movement apparatus. By coupling directed flagellar movement regulating proteins to a '''novel synthetic light-sensitive spatial localization system''', their activity can be controlled reversibly. A light-sensitive dimerizing complex fused to this regulating proteins at a spatially fixed location is induced by light pulses and therefore localization of the two molecules can be manipulated.  Tumbling / directed flagellar movement rates are monitored by image processing algorithms, which are linked to the light-pulse generator. This means that ''E. coli'' tumbling is induced or suppressed simply by pressing a light switch! This synthetic network enables control of single E. coli cells: '''We'll make them move like mindless "Lemmings"''' in the direction they are forced to go!

Revision as of 19:36, 5 October 2010

Welcome to the wiki of the ETH Zurich iGEM team

Project

What is E. lemming?

Click here to learn more.

The core idea of our project is to control chemotaxis of E. coli by means of light! We'll realize this by hijacking and perturbing the tumbling / directed flagellar movement apparatus. By coupling directed flagellar movement regulating proteins to a novel synthetic light-sensitive spatial localization system, their activity can be controlled reversibly. A light-sensitive dimerizing complex fused to this regulating proteins at a spatially fixed location is induced by light pulses and therefore localization of the two molecules can be manipulated. Tumbling / directed flagellar movement rates are monitored by image processing algorithms, which are linked to the light-pulse generator. This means that E. coli tumbling is induced or suppressed simply by pressing a light switch! This synthetic network enables control of single E. coli cells: We'll make them move like mindless "Lemmings" in the direction they are forced to go!

Sponsors

ETHZ Basel sponsors.jpg