Team:TU Darmstadt/strategy

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To easily detect biological toxins we developed a handy device, everybody is able to operate reliably.
 +
By altering the sensorium of <i>E. coli</i> with the help of synthetic biology, the bacteria would release a defined beacon when sensing mycotoxins. This treatment relies on a change of the so called Tar receptors exterior binding site, to specifically react on mycotoxins <sup><span style="color:blue">[1]</span></sup>.
 +
 
 +
By also changing the interior impulse, an explicit beacon can be measured using the interaction of two fluorescent colorants (FRET).
 +
Samples can be given into a self-constructed capsule containing the modified bacteria.
 +
The light-signal inside the capsule is measured using a low-cost and open-source constructed FRET analysing system, as well developed by our team.
 +
 
 +
To illustrate the data in a clear and usable way, the construction of an Android smartphone app is the completion of our project. The application should identify the capsule and apply an online test protocol in order to visualize and compare the data with former tests and share it with customers, leaving the consumer with the opportunity to check different producers on clean manufacturing and production. Consequently, food can be checked on mycotoxins in a cheap and reliable way.
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  <td><img src="https://static.igem.org/mediawiki/2013/b/b9/Darmstadt13_strat_01_G.jpg" alt="1" width="100%"></td>
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  <td><img src="https://static.igem.org/mediawiki/2013/4/4e/Darmstadt13_strat_02_G_.jpg" alt="2"  width="100%" ></td>
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  <td><b>1. Product contaminated by mold fungus</b></td>
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  <td><b>2. Sample given in capsule containing detection organism</b></td>
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  <td><b>3. Biological detection system(inactive)</b></td>
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  </tr>
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  <tr>
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  <td><img src="https://static.igem.org/mediawiki/2013/e/e5/Darmstadt13_strat_04_G.jpg" alt="4"  width="100%" ></td>
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  <td><img src="https://static.igem.org/mediawiki/2013/3/3e/Darmstadt13_strat_05_G.jpg" alt="5"  width="100%"></td>
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  <td><b>4. Biological detection system (activated by myotoxin) </b></td>
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  <td><b>5. Capsule conected to handheld</b></td>
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  <td><b>6. Data can be controlled and analysed by smartphone app</b></td>
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<h2><font size="6" color="#F0F8FF" face="Arial regular">Tar Receptor and CheB</font></h2>
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 +
The Tar protein of <i>E. coli</i> is a receptor protein, that forwards signals from outside into the cell. Its native task is to detect nutritive substances and to induce an active movement towards the source, a so called chemotaxis.
 +
The receptor consists of two identical parts, called homologue monomers and is transmembrane.
 +
The detection is taking place at the external part.
 +
 
 +
When detecting a substance, the receptor is switching form: a conformational change. This causes an alternation inside the cell - the receptor binds proteins transforming the signal into an inner cell cascade.
 +
 
 +
<br>
 +
 
 +
<font size="3" color="#F0F8FF" face="Arial regular">
 +
<p text-aligne:left style="margin-left:50px; margin-right:50px">
 +
 
 +
Here, the first Protein binding to Tar is called CheB.  These two build up the pairs needed for FRET signalling.
 +
 
 +
As the substance does not enter the cell, the Tar receptor is predestined for usage of toxin recognition.
 +
Binding of the Tar receptor has to be absolutely specific to eliminate false positive signals. Therefore, in the external region of the receptor some amino acids have to be changed. A library, where the receptors are tested if the specification for a single toxin has improved, has to be created until a satisfactory version is found.
 +
<br><br>
 +
 
 +
 
 +
<dl class="igemTUD2013gelpicture" style="margin-left:50px;">
 +
<dd><img alt="cheB activesite" src="https://static.igem.org/mediawiki/2013/0/07/Darmstadt13_strat_03._G.jpg" width="10%" height="10%" align="right"></dd>
 +
<dd><font size="2" color="#F0F8FF" face="Arial regular">Biological detection system(inactive)</font></dd>
 +
</dl>
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 +
 
 +
 
 +
<dl class="igemTUD2013gelpicture2" style="margin-right:50px;">
 +
<dd><img alt="cheB" src="https://static.igem.org/mediawiki/2013/e/e5/Darmstadt13_strat_04_G.jpg" width="10%" height="10%" align="right"></dd>
 +
<dd><font size="2" color="#F0F8FF" face="Arial regular">Biological detection system(activated by mycotoxins binding to TAR)</font></dd>
 +
</dl>
 +
 
 +
 
 +
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<br><br><br><br><br><br><br><br><br><br><br><br><br>
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&nbsp; &nbsp; &nbsp;
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<br>
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<br><br><br><br><br>
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<h2><font size="6" color="#F0F8FF" face="Arial regular">FRET</font></h2>
 +
 
 +
<font size="3" color="#F0F8FF" face="Arial regular">
 +
<p text-aligne:left style="margin-left:50px; margin-right:50px">
 +
 
 +
FRET (Förster or Flourescence energy transfer) is a technique to investigate protein interaction in living cells. We adapted this system to use it as a detection element for our selfmade FRET analyser. It works via two chromophores coupled to the prospective proteins. If we use light to excite the cells containing chromophore-coupled proteins, we can get two types of information: in our case the colour orange stands for a negative and red for a positive toxin result. This little trick analyses probes within seconds, hence detection works in real time. An important and often used FRET pair is LSSmOrange and mKate. Their excitation and emission spectra have a compatible overlap.
 +
<br>
 +
<b>In detail:</b> The resulting data gives information about the chromophores connected to the proteins and the distance and angle to each other. The principle relies on a radiation free transition: An excited donor transfers energy to the acceptor by dipole dipole interactions. Here, the given distance between the two molecules needs to be between 0,5 nm and 10 nm for an efficient FRET.
 +
Using the dipole dipole interactions changes in physical structure, bindings and separations can be investigated contemporarily.
 +
</p>
 +
</front>
 +
<br>
 +
<br>
 +
<br>
 +
<h2><font size="6" color="#F0F8FF" face="Arial regular">Handheld and App</font></h2>
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<body>
 +
<font size="3" color="#F0F8FF" face="Arial regular">
 +
<p text-aligne:left style="margin-left:50px; margin-right:50px">
 +
We developed a device that is able to detect the specific light emitted after FRET took place. This device - built into a hendheld and coupled to a smartphone - converts the light into an electric signal and sends it to the smartphone. Additionally, we designed an Android App that can process the data and display it as well.<br><br>
 +
 
 +
An extremely simple optical-sensing technique has been developed appropriate for our application. The sensing system employs two LEDs whereby each one can be used as a light emitter or light detector. The main reason for us to use the pulse based signal  conversion technique is that it leads to better spectral sensitivity; increased and adjustable resolution; reduction in cost, dimensions, power consumption and, additionally, it avoids the need of expensive and precise operation amplifiers, ADCs and other external components<sup><span style="color:blue">[2]</span></sup>. <br><br>
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<font size="3" color="#F0F8FF" face="Arial regular">
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<p text-aligne:left style="margin-left:50px; margin-right:50px">
 +
Our handheld is developed to enable communication between the handheld and a smartphone via Bluetooth a USB. Thereby it allows a simple and wireless operation for the users.
 +
 
 +
 
 +
 
 +
<font size="3" color="#F0F8FF" face="Arial regular">
 +
<p text-aligne:left style="margin-left:50px; margin-right:50px">
 +
The designed App runs on Android phones which are based on linux operation system and is used by about 80 million users worldwide. The App can be downloaded for free (<a href="https://play.google.com/store/apps/details?id=de.tudarmstadt.se.igem&hl=en/">here</a>). 
 +
 
 +
 
 +
<dl class="igemTUD2013gelpicture" style="margin-left:50px;">
 +
<dd><img alt="cheB activesite" src="https://static.igem.org/mediawiki/2013/3/3e/Darmstadt13_strat_05_G.jpg" width="10%" height="10%" align="right"></dd>
 +
<dd><font size="2" color="#F0F8FF" face="Arial regular">Capsule conected to handheld</font></dd>
 +
</dl>
 +
 
 +
<dl class="igemTUD2013gelpicture2" style="margin-right:50px;">
 +
<dd><img alt="cheB" src="https://static.igem.org/mediawiki/2013/5/5a/Darmstadt13_strat_06_G.jpg" width="10%" height="10%" align="right"></dd>
 +
<dd><font size="2" color="#F0F8FF" face="Arial regular">Data can be controlled and analysed by smartphone app</font></dd>
 +
</dl>
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<p>
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<br><br><br>
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<br><br><br><br>
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<br><br><br><br>
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</p>
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<br><br><br><br><br><br><br>
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<h2><font size="6" color="#F0F8FF" face="Arial regular">References</font></h2>
 +
</div>
 +
<ol>
 +
<li style="margin-left:15px; margin-right:50px; text-align:justify">Derr, P. B., 2006 <i>Changing the Specificity of a Bacterial Chemoreceptor.</i> Journal of Molecular Biology, 923–932</li>
 +
<li style="margin-left:15px; margin-right:50px; text-align:justify">Stojanovic, R.; Karadaglic, D.; 2007 <i>An optical sensing approach based on light emitting diodes.</i> Journal of Physics: Conference Series 76 012054</li>
 +
</ol>
 +
 
 +
</front>
 +
<br><br>
 +
<br>
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</p>
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</front>
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Latest revision as of 02:52, 5 October 2013







The Strategy

To easily detect biological toxins we developed a handy device, everybody is able to operate reliably. By altering the sensorium of E. coli with the help of synthetic biology, the bacteria would release a defined beacon when sensing mycotoxins. This treatment relies on a change of the so called Tar receptors exterior binding site, to specifically react on mycotoxins [1]. By also changing the interior impulse, an explicit beacon can be measured using the interaction of two fluorescent colorants (FRET). Samples can be given into a self-constructed capsule containing the modified bacteria. The light-signal inside the capsule is measured using a low-cost and open-source constructed FRET analysing system, as well developed by our team. To illustrate the data in a clear and usable way, the construction of an Android smartphone app is the completion of our project. The application should identify the capsule and apply an online test protocol in order to visualize and compare the data with former tests and share it with customers, leaving the consumer with the opportunity to check different producers on clean manufacturing and production. Consequently, food can be checked on mycotoxins in a cheap and reliable way.



Tar Receptor and CheB

The Tar protein of E. coli is a receptor protein, that forwards signals from outside into the cell. Its native task is to detect nutritive substances and to induce an active movement towards the source, a so called chemotaxis. The receptor consists of two identical parts, called homologue monomers and is transmembrane. The detection is taking place at the external part. When detecting a substance, the receptor is switching form: a conformational change. This causes an alternation inside the cell - the receptor binds proteins transforming the signal into an inner cell cascade.

Here, the first Protein binding to Tar is called CheB. These two build up the pairs needed for FRET signalling. As the substance does not enter the cell, the Tar receptor is predestined for usage of toxin recognition. Binding of the Tar receptor has to be absolutely specific to eliminate false positive signals. Therefore, in the external region of the receptor some amino acids have to be changed. A library, where the receptors are tested if the specification for a single toxin has improved, has to be created until a satisfactory version is found.

cheB activesite
Biological detection system(inactive)
cheB
Biological detection system(activated by mycotoxins binding to TAR)


















     







FRET

FRET (Förster or Flourescence energy transfer) is a technique to investigate protein interaction in living cells. We adapted this system to use it as a detection element for our selfmade FRET analyser. It works via two chromophores coupled to the prospective proteins. If we use light to excite the cells containing chromophore-coupled proteins, we can get two types of information: in our case the colour orange stands for a negative and red for a positive toxin result. This little trick analyses probes within seconds, hence detection works in real time. An important and often used FRET pair is LSSmOrange and mKate. Their excitation and emission spectra have a compatible overlap.
In detail: The resulting data gives information about the chromophores connected to the proteins and the distance and angle to each other. The principle relies on a radiation free transition: An excited donor transfers energy to the acceptor by dipole dipole interactions. Here, the given distance between the two molecules needs to be between 0,5 nm and 10 nm for an efficient FRET. Using the dipole dipole interactions changes in physical structure, bindings and separations can be investigated contemporarily.




Handheld and App

We developed a device that is able to detect the specific light emitted after FRET took place. This device - built into a hendheld and coupled to a smartphone - converts the light into an electric signal and sends it to the smartphone. Additionally, we designed an Android App that can process the data and display it as well.

An extremely simple optical-sensing technique has been developed appropriate for our application. The sensing system employs two LEDs whereby each one can be used as a light emitter or light detector. The main reason for us to use the pulse based signal conversion technique is that it leads to better spectral sensitivity; increased and adjustable resolution; reduction in cost, dimensions, power consumption and, additionally, it avoids the need of expensive and precise operation amplifiers, ADCs and other external components[2].

Our handheld is developed to enable communication between the handheld and a smartphone via Bluetooth a USB. Thereby it allows a simple and wireless operation for the users.

The designed App runs on Android phones which are based on linux operation system and is used by about 80 million users worldwide. The App can be downloaded for free (here).

cheB activesite
Capsule conected to handheld
cheB
Data can be controlled and analysed by smartphone app























References

  1. Derr, P. B., 2006 Changing the Specificity of a Bacterial Chemoreceptor. Journal of Molecular Biology, 923–932
  2. Stojanovic, R.; Karadaglic, D.; 2007 An optical sensing approach based on light emitting diodes. Journal of Physics: Conference Series 76 012054



 

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