Ljubljana, Slovenia 2006/Project & Model

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<table cellpadding="10">
<table cellpadding="10">
<tr><th>[[Ljubljana, Slovenia 2006|Home]]</th>
<tr><th>[[Ljubljana, Slovenia 2006|Home]]</th>
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<th>[[Ljubljana, Slovenia 2006/Background and Signalling Pathway|Background and Signalling Pathway]]</th>
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<th>[[Ljubljana, Slovenia 2006/Background and Signalling Pathway|Background and Signaling Pathway]]</th>
<th>[[Ljubljana, Slovenia 2006/Methods|Methods]]</th>
<th>[[Ljubljana, Slovenia 2006/Methods|Methods]]</th>
<th>[[Ljubljana, Slovenia 2006/Results & Conclusions|Results & Conclusions]]</th>
<th>[[Ljubljana, Slovenia 2006/Results & Conclusions|Results & Conclusions]]</th>
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<h1>Project ideas</h1>
<h1>Project ideas</h1>
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Reasearch in the Laboratory of Biotechnology at the National institute of Chemisty, where most of our instructors come from and wheer most of the experimental work was conducted, is in the area of molecular immunology, specifically interactions in the Toll-like receptor signaling to microbial infections. This determined the selection of the eukaryotic system as our arena of synthetic biology "sandbox". besides, several contributions at the Synthetic biology meetings demonstrated that mammalian cell engineering  
+
Reasearch in the Laboratory of Biotechnology at the National institute of Chemisty, where most of our instructors come from and where most of the experimental work was conducted, is in the area of molecular immunology, specifically interactions in the Toll-like receptor signaling to microbial infections. This determined the selection of the eukaryotic system as our arena of synthetic biology "sandbox". besides, several contributions at the Synthetic biology meetings demonstrated that mammalian cell engineering  
In the beginning we have discussed following project ideas:
In the beginning we have discussed following project ideas:
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<li>Inserton of a logical device into the signaling pathway to limit the cellular activation by bacterial infection
<li>Inserton of a logical device into the signaling pathway to limit the cellular activation by bacterial infection
- use of dominant negative versions of proteins involved in signaling pathway, which will arrest the signaling pathway thus preventing [[Ljubljana, Slovenia 2006/Terms & References#Terms|NF-&kappa;B]] (transcription factor mentioned above)to translocate to the nucleus
- use of dominant negative versions of proteins involved in signaling pathway, which will arrest the signaling pathway thus preventing [[Ljubljana, Slovenia 2006/Terms & References#Terms|NF-&kappa;B]] (transcription factor mentioned above)to translocate to the nucleus
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- addition of degradation tags to this dominant negative proteins ([[Ljubljana, Slovenia 2006/Terms & References#Terms|PEST sequence]]), which would cause inhibition (negative feedback loop) to be temporal </li>
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- addition of degradation tags to this dominant negative proteins ([[Ljubljana, Slovenia 2006/Terms & References#Terms|PEST sequence]]), which would cause inhibition (negative feedback loop) to be temporal. </li>
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+
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<li>Engineering of the response to pathogens/their PAMPs, which are otherwise not recognized by cells
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- for example a response to beta glucans of fungi</li>
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<li>Engineering of novel interconnections between signaling pathways </li> </ol>
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 +
<li>Engineering of the response to pathogens/their [[Ljubljana, Slovenia 2006/Terms & References#Terms|PAMP]]s, which are otherwise not recognized by cells
 +
- for example a response to beta glucans of fungi.</li>
 +
<li>Engineering of novel interconnections between signaling pathways. </li> </ol>
 +
<br>
<h1>Selected project</h1>
<h1>Selected project</h1>
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[[Image:sepsa.png|250px|thumb|Figure 1: Infection can lead to sepsis, which is in many cases fatal, but the negative feedback would decrease the imune response.]]
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[[Image:sepsa.png|250px|thumb|<b>Figure 4: Unlimited cell stimulation due to the infection can lead to sepsis, which is in many cases fatal</b>. Introduction of the negative feedback could decrease the immune response.]]
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<p>The basic idea of our project was to introduce a feedback loop in TLR signaling pathway, which would decrease the overwhelming response to the persistent or repeated stimulus with PAMP. However, completly shutting down the response to bacterial stimulation is not recommendable from the view of a host battling the infection. Ideally the feedback loop should decrease the response when it is too high but recover the responsiveness of the system after some time.</p>
+
<p>The basic idea of our project was to introduce a feedback loop in TLR signaling pathway, which would decrease the overwhelming response to the persistent or repeated stimulus with [[Ljubljana, Slovenia 2006/Terms & References#Terms|PAMP]]. However, completly shutting down the response to bacterial stimulation is not recommendable from the view of a host battling the infection. Ideally the feedback loop should decrease the response when it is too high but recover the responsiveness of the system after some time.</p>
-
<p>Inhibition of the overwhelming response could be achieved if PAMP is simultaneously able to activate the immune response and the expression of a [[Ljubljana, Slovenia 2006/Terms & References#Terms|dominant-negative]] adapter protein, that would inactivate PAMP`s signaling pathway. Decreasing the lifetime of the dominant-negative inhibitior by the addition of a rapid degradation tag ([[Ljubljana, Slovenia 2006/Terms & References#Terms|PEST sequence]]) should inactivate the inhibition and restore the responsiveness of the immune system.</p>
+
<p>Inhibition of the overwhelming response could be achieved if [[Ljubljana, Slovenia 2006/Terms & References#Terms|PAMP]] is simultaneously able to activate the immune response and the expression of a [[Ljubljana, Slovenia 2006/Terms & References#Terms|dominant-negative]] adapter protein, that would inactivate [[Ljubljana, Slovenia 2006/Terms & References#Terms|PAMP]]`s signaling pathway. Decreasing the lifetime of the dominant-negative inhibitior by the addition of a rapid degradation tag ([[Ljubljana, Slovenia 2006/Terms & References#Terms|PEST sequence]]) should inactivate the inhibition and restore the responsiveness of the immune system.</p>
 +
 
 +
<p>This idea is similar to the natural mechanism of tolerance, which is already present in living cells and which decreases the response to repeated bacterial stimulations. This natural tolerance is activated slowly, on the order of days and operates through several different mechanisms. Our feedback mechanism (i.e. artificial tolerance) should decrease the response within hours and thus "attack" the signaling pathway at the point, which has not been used in the natural system.</p>
 +
<br>
-
<p>This idea is similar to the natural mechanism of tolerance, which is already present in living cells and which decreases the response to repeated bacterial stimulations. This natural tolerance is activated slowly, on the order of days and operates through several different mechanisms (Figure). Our feedback mechanism (i.e. artificial tolerance) should decrease the response within hours and thus "attack" the signaling pathway at the point, which has not been used in the natural system.</p>
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<h2>Model of the TLR signaling triggered by bacterial infection</h2>
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<h2>Model of the TLR signalling triggered by bacterial infection</h2>
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<h3>[[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]] is the hub of the TLR signaling pathway</h3>
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<h3>[[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]] is the hub of the TLR signalling pathway</h3>
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<p>
<p>
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Figure 2 represents the complexity of cell signalling mediated by TLRs. which contains more than 700 molecules and complexes (Oda, Kitano, Molecular Systems Biology 2006).</p>
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Figure 5 represents the complexity of cell signaling mediated by TLRs. which contains more than 700 molecules and complexes (Oda & Kitano, Molecular Systems Biology, 2006).</p>
<br style="clear:both;"/>
<br style="clear:both;"/>
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[[Image:model1.gif|thumb|center|800px|Figure 2: Comprehensive scheme of the Toll-like receptor signaling of microbial infection.]]
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[[Image:model1.gif|thumb|center|800px|<b>Figure 5: Comprehensive scheme of the Toll-like receptor signaling of microbial infection.</b>]]
<br style="clear:both;"/>
<br style="clear:both;"/>
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[[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]] adapter protein is involved in the signal transduction immediately after ligand-induced TLR oligomerization. This adapter protein is common to most TLRs before the signaling network branches into several phosphpryation cascades. We selected this molecule as the most appropriate target of TLR signaling network engineering (Figures 3 and 4).
+
<p>[[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]] adapter protein is involved in the signal transduction immediately after ligand-induced TLR oligomerization. This adapter protein is common to most TLRs before the signaling network branches into several phosphpryation cascades. We selected this molecule as the most appropriate target of TLR signaling network engineering (Figures 6 and 7).</p>
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[[Image:model2.gif|thumb|left|650px|Figure 3: [[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]] adapter protein connects the response of all TLRs and represents the »bottleneck« of the system (shaded area).]]
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[[Image:model2.gif|thumb|left|650px|<b>Figure 6: [[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]] adapter protein connects the response of all TLRs and represents the »bottleneck« of the system (shaded area).</b>]]
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[[Image:model3.gif|thumb|right|200px|Figure 4: Schematic representation of [[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]] as the hub of TLR signaling shaped like a bow tie .]]
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[[Image:model3.gif|thumb|right|200px|<b>Figure 7: Schematic representation of the [[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]] as the hub of TLR signaling shaped like a bow tie.</b>]]
<br style="clear:both;"/>
<br style="clear:both;"/>
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<h3>Construction of the model</h3>
<h3>Construction of the model</h3>
<p>
<p>
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Model of the TLR signaling was prepared in CellDesigner. Signaling steps, where the response remains the same were assembled into one block (Signaling cascade), whose activation directly affects the [[Ljubljana, Slovenia 2006/Terms & References#Terms|NF-&kappa;B]] translocation. Our engineered feedback loop is inserted as a transcriptional activation of [[Ljubljana, Slovenia 2006/Terms & References#Terms|dnMyD88]] protein domain (red block in Figure 6).</p>
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Model of the TLR signaling was prepared in CellDesigner. Signaling steps, where the response remains the same were assembled into one block (Signaling cascade), whose activation directly affects the [[Ljubljana, Slovenia 2006/Terms & References#Terms|NF-&kappa;B]] translocation. Our engineered feedback loop is inserted as a transcriptional activation of [[Ljubljana, Slovenia 2006/Terms & References#Terms|dnMyD88]] protein domain (red block in Figure 8).</p>
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[[Image:model12a.gif|left|thumb|400px|Figure 5: Simplified model of Toll-like receptor signaling constructed in CellDesigner.]]
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[[Image:model12a.gif|left|thumb|400px|<b>Figure 8: Simplified model of Toll-like receptor signaling constructed in CellDesigner.</b>]]
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[[Image:model12.gif|right|thumb|400px|Figure 6: Model of TLR signaling with additional feedback loop for the inhibition of [[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]].]]
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[[Image:model12.gif|right|thumb|400px|<b>Figure 9: Model of TLR signaling with additional feedback loop for the inhibition of [[Ljubljana, Slovenia 2006/Terms & References#Terms|MyD88]].</b>]]
<br style="clear:both;"/>
<br style="clear:both;"/>
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<p>Simulation of cellular response to TLR stimulation by a pulse of PAMP (e.g. flagellin). Signaling cascade results in the transient translocation of [[Ljubljana, Slovenia 2006/Terms & References#Terms|NF-&kappa;B]] into the cell nucleus (green) and in the production of inflammatory mediators. Repeated pulse after some time results in the repeated activation and accumulation of inflammatory mediators.</p>
+
<p>Simulation of cellular response to TLR stimulation by a pulse of [[Ljubljana, Slovenia 2006/Terms & References#Terms|PAMP]] (e.g. flagellin). When available parameters were taken from the literaturte (Selvarajoo, 2006). Signaling cascade results in the transient translocation of [[Ljubljana, Slovenia 2006/Terms & References#Terms|NF-&kappa;B]] into the cell nucleus (green) and in the production of inflammatory mediators. Repeated pulse after some time results in the repeated activation and accumulation of inflammatory mediators.</p>
<br style="clear:both;"/>
<br style="clear:both;"/>
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[[Image:model6.gif|thumb|left|400px|Figure 7: Simulation of the cell response to the bacterial stimulus PAMP (grey) – transient translocation of the [[Ljubljana, Slovenia 2006/Terms & References#Terms|NF-&kappa;B]] into the nucleus (green), production of stimulatory mediators (orange).]]
+
[[Image:model6.gif|thumb|left|400px|<b>Figure 10: Simulation of the cell response to the bacterial stimulus [[Ljubljana, Slovenia 2006/Terms & References#Terms|PAMP</b>]] (grey) – transient translocation of the [[Ljubljana, Slovenia 2006/Terms & References#Terms|NF-&kappa;B]] into the nucleus (green), production of stimulatory mediators (orange).]]
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[[Image:model7.gif|thumb|right|400px|Figure 8: Simulation of the repeated stimulation by PAMP (grey)  - Amount of inflammatory mediators increases (orange).]]
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[[Image:model7.gif|thumb|right|400px|<b>Figure 11: Simulation of the repeated cellular stimulation by [[Ljubljana, Slovenia 2006/Terms & References#Terms|PAMP]]</b> (grey)  - the amount of inflammatory mediators increases (orange).]]
<br style="clear:both;"/>
<br style="clear:both;"/>
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<p>Simulation of the TLR signaling response in the system with a feedback device results in the production of inhibitor ([[Ljubljana, Slovenia 2006/Terms & References|dnMyD88]], black) which inhibits cellular activation by a repeated stimulation. Cellular responsiveness resets to the normal response if the inhibitor is rapidly degraded, such as by the addition of a [[Ljubljana, Slovenia 2006/Terms & References|PEST]] motif.</p>
<p>Simulation of the TLR signaling response in the system with a feedback device results in the production of inhibitor ([[Ljubljana, Slovenia 2006/Terms & References|dnMyD88]], black) which inhibits cellular activation by a repeated stimulation. Cellular responsiveness resets to the normal response if the inhibitor is rapidly degraded, such as by the addition of a [[Ljubljana, Slovenia 2006/Terms & References|PEST]] motif.</p>
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[[Image:model8.gif|thumb|left|400px|Figure 9: Addition of a feedback loop to start production of inhibitory [[Ljubljana, Slovenia 2006/Terms & References#Terms|dnMyD88]]( (black) – cell does not respond to the repeated stimulation.]]
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[[Image:model8.gif|thumb|left|400px|<b>Figure 12: Introduction of the feedback loop to initiate the production of inhibitory [[Ljubljana, Slovenia 2006/Terms & References#Terms|dnMyD88]]</b>( (black) – cell does not respond to the repeated stimulation.]]
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[[Image:model9.gif|thumb|right|400px|Figure 10: Feedback loop with rapid degradation of the inhibitor ([[Ljubljana, Slovenia 2006/Terms & References#Terms|dnMyD88]] with PEST sequence - black) – responsiveness of the system is again completely restored.]]
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[[Image:model9.gif|thumb|right|400px|<b>Figure 13: Feedback loop with rapid degradation of the inhibitor ([[Ljubljana, Slovenia 2006/Terms & References#Terms|dnMyD88]] with PEST sequence</b> - black) – responsiveness of the system is again restored to a full extent.]]
<br style="clear:both;"/>
<br style="clear:both;"/>
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[[Image:model10.gif|thumb|left|400px|Figure 11: Speed of the degradation of [[Ljubljana, Slovenia 2006/Terms & References#Terms|dnMyD88]] could modulate the responsiveness of the system to repeated (or continuous) challenge by TLR agonists.]]
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[[Image:model10.gif|thumb|left|400px|<b>Figure 14: Speed of the degradation of [[Ljubljana, Slovenia 2006/Terms & References#Terms|dnMyD88]] could modulate the responsiveness of the system to repeated (or continuous) challenge by TLR agonists.</b>]]
<br style="clear:both;"/>
<br style="clear:both;"/>
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<table cellpadding="10">
<table cellpadding="10">
<tr><th>[[Ljubljana, Slovenia 2006|Home]]</th>
<tr><th>[[Ljubljana, Slovenia 2006|Home]]</th>
-
<th>[[Ljubljana, Slovenia 2006/Background and Signalling Pathway|Background and Signalling Pathway]]</th>
+
<th>[[Ljubljana, Slovenia 2006/Background and Signalling Pathway|Background and Signaling Pathway]]</th>
<th>[[Ljubljana, Slovenia 2006/Methods|Methods]]</th>
<th>[[Ljubljana, Slovenia 2006/Methods|Methods]]</th>
<th>[[Ljubljana, Slovenia 2006/Results & Conclusions|Results & Conclusions]]</th>
<th>[[Ljubljana, Slovenia 2006/Results & Conclusions|Results & Conclusions]]</th>

Latest revision as of 14:44, 31 October 2006

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Contents

Project ideas

Reasearch in the Laboratory of Biotechnology at the National institute of Chemisty, where most of our instructors come from and where most of the experimental work was conducted, is in the area of molecular immunology, specifically interactions in the Toll-like receptor signaling to microbial infections. This determined the selection of the eukaryotic system as our arena of synthetic biology "sandbox". besides, several contributions at the Synthetic biology meetings demonstrated that mammalian cell engineering

In the beginning we have discussed following project ideas:

  1. Inserton of a logical device into the signaling pathway to limit the cellular activation by bacterial infection - use of dominant negative versions of proteins involved in signaling pathway, which will arrest the signaling pathway thus preventing NF-κB (transcription factor mentioned above)to translocate to the nucleus - addition of degradation tags to this dominant negative proteins (PEST sequence), which would cause inhibition (negative feedback loop) to be temporal.
  2. Engineering of the response to pathogens/their PAMPs, which are otherwise not recognized by cells - for example a response to beta glucans of fungi.
  3. Engineering of novel interconnections between signaling pathways.


Selected project

Figure 4: Unlimited cell stimulation due to the infection can lead to sepsis, which is in many cases fatal. Introduction of the negative feedback could decrease the immune response.

The basic idea of our project was to introduce a feedback loop in TLR signaling pathway, which would decrease the overwhelming response to the persistent or repeated stimulus with PAMP. However, completly shutting down the response to bacterial stimulation is not recommendable from the view of a host battling the infection. Ideally the feedback loop should decrease the response when it is too high but recover the responsiveness of the system after some time.

Inhibition of the overwhelming response could be achieved if PAMP is simultaneously able to activate the immune response and the expression of a dominant-negative adapter protein, that would inactivate PAMP`s signaling pathway. Decreasing the lifetime of the dominant-negative inhibitior by the addition of a rapid degradation tag (PEST sequence) should inactivate the inhibition and restore the responsiveness of the immune system.

This idea is similar to the natural mechanism of tolerance, which is already present in living cells and which decreases the response to repeated bacterial stimulations. This natural tolerance is activated slowly, on the order of days and operates through several different mechanisms. Our feedback mechanism (i.e. artificial tolerance) should decrease the response within hours and thus "attack" the signaling pathway at the point, which has not been used in the natural system.


Model of the TLR signaling triggered by bacterial infection

MyD88 is the hub of the TLR signaling pathway

Figure 5 represents the complexity of cell signaling mediated by TLRs. which contains more than 700 molecules and complexes (Oda & Kitano, Molecular Systems Biology, 2006).


Figure 5: Comprehensive scheme of the Toll-like receptor signaling of microbial infection.



MyD88 adapter protein is involved in the signal transduction immediately after ligand-induced TLR oligomerization. This adapter protein is common to most TLRs before the signaling network branches into several phosphpryation cascades. We selected this molecule as the most appropriate target of TLR signaling network engineering (Figures 6 and 7).

Figure 6: MyD88 adapter protein connects the response of all TLRs and represents the »bottleneck« of the system (shaded area).
Figure 7: Schematic representation of the MyD88 as the hub of TLR signaling shaped like a bow tie.


Construction of the model

Model of the TLR signaling was prepared in CellDesigner. Signaling steps, where the response remains the same were assembled into one block (Signaling cascade), whose activation directly affects the NF-κB translocation. Our engineered feedback loop is inserted as a transcriptional activation of dnMyD88 protein domain (red block in Figure 8).

Figure 8: Simplified model of Toll-like receptor signaling constructed in CellDesigner.
Figure 9: Model of TLR signaling with additional feedback loop for the inhibition of MyD88.


Simulation of cellular response to TLR stimulation by a pulse of PAMP (e.g. flagellin). When available parameters were taken from the literaturte (Selvarajoo, 2006). Signaling cascade results in the transient translocation of NF-κB into the cell nucleus (green) and in the production of inflammatory mediators. Repeated pulse after some time results in the repeated activation and accumulation of inflammatory mediators.


Figure 10: Simulation of the cell response to the bacterial stimulus PAMP (grey) – transient translocation of the NF-κB into the nucleus (green), production of stimulatory mediators (orange).
Figure 11: Simulation of the repeated cellular stimulation by PAMP (grey) - the amount of inflammatory mediators increases (orange).


Simulation of the TLR signaling response in the system with a feedback device results in the production of inhibitor (dnMyD88, black) which inhibits cellular activation by a repeated stimulation. Cellular responsiveness resets to the normal response if the inhibitor is rapidly degraded, such as by the addition of a PEST motif.

Figure 12: Introduction of the feedback loop to initiate the production of inhibitory dnMyD88( (black) – cell does not respond to the repeated stimulation.
Figure 13: Feedback loop with rapid degradation of the inhibitor (dnMyD88 with PEST sequence - black) – responsiveness of the system is again restored to a full extent.


Figure 14: Speed of the degradation of dnMyD88 could modulate the responsiveness of the system to repeated (or continuous) challenge by TLR agonists.



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