Team:TU Munich/project

From 2011.igem.org

(Difference between revisions)
(Created page with "{{Team:TU_Munich/Header}} <html> <body> <div id="social" class="content"> <table border="0"> <td width="60%"> <div class="subcontent ui-corner-all"> <b>General Project Outline...")
m
 
(28 intermediate revisions not shown)
Line 4: Line 4:
<body>
<body>
<div id="social" class="content">
<div id="social" class="content">
-
<table border="0">
+
<div class="subcontent ui-corner-all subproject" style="clear:both;">
-
<td width="60%">
+
 
-
<div class="subcontent ui-corner-all">
+
   <h2>Optogenetical AND-Gate</h2>
-
   <b>General Project Outline</b>
+
<a href="https://static.igem.org/mediawiki/2011/9/9d/Skizzeweb.jpg" rel="lightbox" title="Scheme"><img src="https://static.igem.org/mediawiki/2011/9/9d/Skizzeweb.jpg" alt="plasmid1" style="float:right;width:350px;padding-left:20px;padding-bottom:30px;margin-top:-15px;"></a>
-
  <hr />
+
-
  <p>This year, we aim to develop a light-controlled 3D-printer by innovative utilization of optogenetics. As a first step, we want to develop a genetic logical AND-gate sensitive to light of two different wavelengths (e.g. blue and red light). The bacteria are then immobilized in a transparent gel matrix, where they can be precisely actuated when hit by both blue and red light at the same time. If both of these inputs are positive, gene expression is induced. Various different gene products can be expressed using this system. For example, a simple colored pigment will allow us to create colored three dimensional objects, while expressing collagen and consecutive biomineralization and generation of hydroxylapatite could be used to create bone.</p>
+
-
  <br>
+
-
  <b>Optogenetical AND-Gate</b>
+
-
  <hr />
+
   <p>In order to be able to adress our immobilized cells in a defined spatiotemporal manner, we require two signals which will be irradiated into the gel block from two different directions. For this purpose, we will introduce an optogenetical AND-Gate into the bacteria. This logical gate is based on amber stop-codon suppression via the non-canonical tRNA supD. A light sensitive promoter induces the expression of a mRNA coding for a T7-polymerase, which can only be translated by ribosomes if the correct amber tRNA is present. The tRNA is expressed by a second light-sensitive promoter. Thus, only cells which receive both signals produce the desired substances.</p>
   <p>In order to be able to adress our immobilized cells in a defined spatiotemporal manner, we require two signals which will be irradiated into the gel block from two different directions. For this purpose, we will introduce an optogenetical AND-Gate into the bacteria. This logical gate is based on amber stop-codon suppression via the non-canonical tRNA supD. A light sensitive promoter induces the expression of a mRNA coding for a T7-polymerase, which can only be translated by ribosomes if the correct amber tRNA is present. The tRNA is expressed by a second light-sensitive promoter. Thus, only cells which receive both signals produce the desired substances.</p>
   <br>
   <br>
-
   <b>Light Sensory Domains</b>
+
   <h2>Light Sensory Domains</h2>
-
  <hr />
+
   <p> We chose the promoter of YcgF/E as blue light sensor and Cph8 as red light sensor. In the beginning, we also thought about using ccaR/ccaS as green-light sensor (instead of either YcgF/E or Cph8). The reason we decided to use a combination of the red and blue light sensor systems, is the great difference between the absorbtion maxima of the light sensory domains. We expect that this assembly will be the one with the lowest amount of unspecific gene expression which could occur due to overlapping of the absorption spectrums of the sensory domains.</p>
-
   <p>We have three candidates which can be used as light sensitive promoters: the promoter of YcgF/E as blue light sensor, Cph8 as red light sensor, and ccaR/ccaS as green-light sensor. At this point, we are inclined to use a combination of the red and blue light sensor systems, because of the great difference between the absorbtion maxima of the light sensory domains. We expect that this assembly will be the one with the lowest amount of unspecific gene expression which could occur due to overlapping of the absorption spectrums of the sensory domains.</p>
+
   <br>
   <br>
-
   <b>Progress</b>
+
   <h2>Progress</h2>
-
  <hr />
+
   <p>Construct design and cloning has been completed while characterization is still in progress. Further more, we found a suitable solid matrix, which is on the one hand, clear enough to be penetrated by light beams without refracting them and, on the other hand, solidifies at a temperature that is low enough to allow for cell immobilization without harming the bacteria.</p>  
-
   <p>Construct design has been completed while cloning is still in progress. Further more, we found a suitable solid matrix which is, on the one hand, clear enough to be penetrated by light beams without refracting them and, on the other hand, solidifies at a temperature that is low enough to allow for cell immobilization without harming the bacteria.</p>  
+
</div>
</div>
-
</td>
 
-
<td width="40%">
 
-
<ul class="bacnav">
 
-
        <a href="https://2011.igem.org/Team:TU_Munich/project/introduction"><li>Introduction</li></a>
 
-
        <a href="https://2011.igem.org/Team:TU_Munich/project/modeling"><li>Modeling</li></a>
 
-
        <a href="https://2011.igem.org/Team:TU_Munich/project/human"><li>Human Practice</li></a>
 
-
        <a href="https://2011.igem.org/Team:TU_Munich/project/data"><li>Data Page</li></a>
 
-
</ul>
 
-
</td>
 
-
</table>
 
</div>
</div>

Latest revision as of 00:32, 22 September 2011

Optogenetical AND-Gate

plasmid1

In order to be able to adress our immobilized cells in a defined spatiotemporal manner, we require two signals which will be irradiated into the gel block from two different directions. For this purpose, we will introduce an optogenetical AND-Gate into the bacteria. This logical gate is based on amber stop-codon suppression via the non-canonical tRNA supD. A light sensitive promoter induces the expression of a mRNA coding for a T7-polymerase, which can only be translated by ribosomes if the correct amber tRNA is present. The tRNA is expressed by a second light-sensitive promoter. Thus, only cells which receive both signals produce the desired substances.


Light Sensory Domains

We chose the promoter of YcgF/E as blue light sensor and Cph8 as red light sensor. In the beginning, we also thought about using ccaR/ccaS as green-light sensor (instead of either YcgF/E or Cph8). The reason we decided to use a combination of the red and blue light sensor systems, is the great difference between the absorbtion maxima of the light sensory domains. We expect that this assembly will be the one with the lowest amount of unspecific gene expression which could occur due to overlapping of the absorption spectrums of the sensory domains.


Progress

Construct design and cloning has been completed while characterization is still in progress. Further more, we found a suitable solid matrix, which is on the one hand, clear enough to be penetrated by light beams without refracting them and, on the other hand, solidifies at a temperature that is low enough to allow for cell immobilization without harming the bacteria.

Retrieved from "http://2011.igem.org/Team:TU_Munich/project"