Team:EPF Lausanne/Overview

From 2014.igem.org

(Difference between revisions)
 
(21 intermediate revisions not shown)
Line 124: Line 124:
<!--Our team has been working on showing that biologically engineered organisms can detect and process signals quickly and efficiently.-->
<!--Our team has been working on showing that biologically engineered organisms can detect and process signals quickly and efficiently.-->
-
Biological responses can be quick and precise! This is the message that our team wants to conveyWith this in mind, our team brought forward a novel idea:  
+
Biological responses can be quick and precise! This is the message that our team wants to convey. With this in mind, our team brought forward a novel idea:  
<br />
<br />
<p style="border-style:solid; border-color:#120A2A;padding: 25px; background-color:#A5D2DA">
<p style="border-style:solid; border-color:#120A2A;padding: 25px; background-color:#A5D2DA">
-
Combining Protein Complementation techniques with biosensors and microfluidics, allows fast spatiotemporal analysis of bacterial/yeast responses to stimuli.
+
Combining Protein Complementation techniques with biosensors and microfluidics allows fast spatiotemporal analysis of bacterial/yeast responses to stimuli.
</p>
</p>
Line 145: Line 145:
<p class="lead">
<p class="lead">
-
Our team explored this hypothesis by engineering two stress related pathways in <i>E. coli</i> and <i>S. cerevisiae</i> with in mind the development of a BioPad: a biological touchscreen consisting of a microfluidic chip, touch responsive bacteria/yeast, and a signal detector. Learn more about <a href="#howitworks">how the BioPad works !</a> </p>
+
Our team explored this hypothesis by engineering two stress related pathways in <i>E. coli</i> and <i>S. cerevisiae</i> with in mind the development of a BioPad: a biological touchscreen consisting of a microfluidic chip, touch-responsive bacteria/yeast, and a signal detector. Learn more about <a href="#howitworks">how the BioPad works !</a> </p>
Line 163: Line 163:
<br/>
<br/>
-
<div  class="cntr img-border">
+
<div  class="cntr">
-
<a href="https://static.igem.org/mediawiki/2014/f/fd/CpxR-HOG.jpg" data-lightbox="cpxr" data-title="EPFL microfluidic chips">
+
<a href="https://static.igem.org/mediawiki/2014/f/fd/CpxR-HOG.jpg" data-lightbox="cpxr" data-title="CpxR-HOG">
-
<img src="https://static.igem.org/mediawiki/2014/f/fd/CpxR-HOG.jpg" alt="touch response" class="img-responsive" /></a>
+
<img src="https://static.igem.org/mediawiki/2014/f/fd/CpxR-HOG.jpg" alt="touch response" class="img-responsive img-border" /></a>
</div>
</div>
Line 172: Line 172:
<div class="pull-left img-left">
<div class="pull-left img-left">
<a href="https://static.igem.org/mediawiki/2014/d/d8/EPFLmicrofluidics.JPG" data-lightbox="image-1" data-title="EPFL microfluidic chips"><img src="https://static.igem.org/mediawiki/2014/d/d8/EPFLmicrofluidics.JPG" width="250" class="img-border"></a>
<a href="https://static.igem.org/mediawiki/2014/d/d8/EPFLmicrofluidics.JPG" data-lightbox="image-1" data-title="EPFL microfluidic chips"><img src="https://static.igem.org/mediawiki/2014/d/d8/EPFLmicrofluidics.JPG" width="250" class="img-border"></a>
 +
<figcaption class="cntr">EPFL microfluidic chips</figcaption>
</div>
</div>
<p class="lead">
<p class="lead">
-
Our project also includes an extensive <b>microfluidics section</b>. Our self designed chips helped us improve precision, safety, and quantification methods used throughout the project. To learn more about the microfluidic components of our project check out <a  target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Microfluidics">this link.</a></p>
+
Our project also includes an extensive <b>microfluidics section</b>. Our self designed chips helped us improve precision, safety and quantification methods used throughout the project. To learn more about the microfluidic components of our project check out <a  target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Microfluidics">this link.</a></p>
<div class="pull-right img-right">
<div class="pull-right img-right">
<img src="http://www.raspberrypi.org/wp-content/uploads/2011/07/RaspiModelB.png" alt="first" width="200" class="img-border">
<img src="http://www.raspberrypi.org/wp-content/uploads/2011/07/RaspiModelB.png" alt="first" width="200" class="img-border">
 +
<figcaption class="cntr">Raspberry Pi</figcaption>
</div>
</div>
<p class="lead">
<p class="lead">
<br />
<br />
-
Last but not least, we designed a <b>novel signal detector</b> ! To make signal detection more practical we developed an automatised cheap tracking system made of a mini-computer (Raspberry Pi) and a mini-HD camera. More details concerning this the BioPad detector can be found <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Hardware">here.</a>
+
Last but not least, we designed a <b>novel signal detector</b>! To make signal detection more practical we developed an automatised cheap tracking system made of a mini-computer (Raspberry Pi) and a mini-HD camera. More details concerning the BioPad detector can be found <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Hardware">here.</a>
<br /></p>
<br /></p>
Line 224: Line 226:
<a href="https://static.igem.org/mediawiki/2014/b/b7/Puce_petit.jpg" data-lightbox="image-0" data-title="A potential BioPad">
<a href="https://static.igem.org/mediawiki/2014/b/b7/Puce_petit.jpg" data-lightbox="image-0" data-title="A potential BioPad">
<img src="https://static.igem.org/mediawiki/2014/b/b7/Puce_petit.jpg" alt="Potential biopad" height="200" class="img-border" /></a>
<img src="https://static.igem.org/mediawiki/2014/b/b7/Puce_petit.jpg" alt="Potential biopad" height="200" class="img-border" /></a>
 +
<figcaption class="cntr">A potential BioPad</figcaption>
</div>
</div>
Line 234: Line 237:
The histidine kinase sensor CpxA auto-phosphorylates and transfers its phosphate to its corresponding relay protein, CpxR, resulting in its dimerization. We engineered the pathway, by fusing split reporter protein fragments to the CpxR (IFP1.4). This allows the two fragments to remain inactive until physical interaction of CpxR (stimulated by envelope stress) leads to the proper folding of IFP1.4  and reconstitution of its fluorescent properties. As the reconstitution of the split fragments of IFP1.4 are reversible, the system can be shutdown upon stress removal (CpxA changes conformation to become a phosphatase and induces CpxR’s dissociation).<br/> <br/>  
The histidine kinase sensor CpxA auto-phosphorylates and transfers its phosphate to its corresponding relay protein, CpxR, resulting in its dimerization. We engineered the pathway, by fusing split reporter protein fragments to the CpxR (IFP1.4). This allows the two fragments to remain inactive until physical interaction of CpxR (stimulated by envelope stress) leads to the proper folding of IFP1.4  and reconstitution of its fluorescent properties. As the reconstitution of the split fragments of IFP1.4 are reversible, the system can be shutdown upon stress removal (CpxA changes conformation to become a phosphatase and induces CpxR’s dissociation).<br/> <br/>  
-
The BioPad also includes a signal detector. The BioPad Detector is composed of an inexpensive credit card-sized single-board computer called Raspberry Pi, a highly sensitive digital camera with appropriate light filters, and a light-emitting source. It identifies and processes the position of the light/fluorescence emitted by the BioPad. The information about the position of the light relative to chip is then used to control the associated electronic device. <br/> <br/>
+
The BioPad also includes a signal detector. This detector is composed of an inexpensive credit card-sized single-board computer called Raspberry Pi, a highly sensitive digital camera with appropriate light filters, and a light-emitting source. It identifies and processes the position of the light/fluorescence emitted by the BioPad. The information about the position of the light relative to chip is then used to control the associated electronic device. <br/>
-
<!--
 
-
Our self-designed PDMS microfluidic chip, the BioPad, is made of hundreds of compartments representing "pixels." Each 30µm x 30µm x 3µm compartment contains a few layers of <i>E. coli</i>. When the surface of the chip is touched, a deformation of the chip - and thus of the compartments - leads to cellular membrane shear stress and protein aggregation/misfolding in the periplasm.
 
-
<br />
 
-
 
-
The aggregated/misfolded proteins are then sensed by the histidine kinase CpxA sensor, which auto-phosphorylates and transfers its phosphate to its corresponding relay protein, CpxR. Upon phosphorylation, CpxR homo-dimerizes.
 
-
 
-
<br />
 
-
Our engineered bacteria contain CpxR proteins fused to split fluorescent protein fragments (split IFP1.4) via a 10-amino acid, 2x GGGGS flexible linker. This allows us to detect CpxR dimerization, synonymous periplasmic stress and touch. Moreover, the split protein fragments are reversible. Therefore, when stress is removed, CpxA changes conformation and dephosphorylates CpxR allowing it to dissociate. The signal is shutdown and darkness returns The BioPad Detector (composed of an inexpensive CMOS called Raspberry Pi, a highly sensitive digital camera with appropriate light filters, and a light emitting source) identifies and processes the position of the light/fluorescence emitted by the BioPad. This information about the position of the light relative to chip is then used to control the associated electronic device.
 
-
</p>
 
-
-->
 
Line 288: Line 281:
<br/>
<br/>
The <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Yeast">HOG pathway</a> controls the response to osmotic stress in yeast cells.
The <a target="_blank" href="https://2014.igem.org/Team:EPF_Lausanne/Yeast">HOG pathway</a> controls the response to osmotic stress in yeast cells.
-
Like bacteria, our modified <i>S. cerevisiae</i> cells can be loaded into the PDMS microfluidic chips we have designed. Thus cells are confined in small compartments made of a rather soft material. When the surface of the chip is touched, it leads to a deformation of the chip and its chambers. Since the HOG pathway is reactive to turgor pressure, the mechanical pressure applied activates it. Upon induction of the pathway, which is a classical MAP kinase pathway, PBS2 – a MAPKK – is phosphorylated and binds HOG1 – a MAPK – and in turn phosphorylates it.
+
Like bacteria, our modified <i>S. cerevisiae</i> cells can be loaded into the PDMS microfluidic chips we have designed. Thus cells are confined in small compartments made of a soft material. When the surface of the chip is touched, it leads to a deformation of the chip and its chambers. Since the HOG pathway is reactive to turgor pressure, the mechanical pressure applied activates it. Upon induction of the pathway, which is a classical MAP kinase pathway, PBS2 – a MAPKK – is phosphorylated and binds HOG1 – a MAPK – and in turn phosphorylates it.
</p>
</p>
-
<a href="https://static.igem.org/mediawiki/2014/7/7b/Schema_split.png" data-lightbox="img1" data-title="Schema of Hog1/Pbs2 split sfGFP and split rLuc">
+
<div class="pull-left img-left" style="width:55%">
-
<img src="https://static.igem.org/mediawiki/2014/7/7b/Schema_split.png" width="55%" alt="" class="pull-left img-left img-border"></a>
+
<a href="https://static.igem.org/mediawiki/2014/7/7b/Schema_split.png" data-lightbox="img1" data-title="Figure of Hog1/Pbs2 split sfGFP and split rLuc">
 +
<img src="https://static.igem.org/mediawiki/2014/7/7b/Schema_split.png" alt="" class="img-border" style="width: 100%">
 +
</a>
 +
<figcaption class="cntr">Figure of Hog1/Pbs2 split sfGFP and split rLuc</figcaption>
 +
 
 +
</div>
<p class="lead">
<p class="lead">
-
Therefore, we have fused these two kinases to split fluorescent and luminescent proteins, via a 13-amino acid flexible linker, by homologous recombination. This allows us to detect the phosphorylation of Hog1 by Pbs2 in response to osmotic pressure or touch. We have used split sfGFP and split Renilla luciferase tags on the C-terminals of both proteins.
+
These two kinases were fused to split fluorescent and luminescent proteins, via a 13-amino acid flexible linker, by homologous recombination. This allowed us to detect the phosphorylation of Hog1 by Pbs2 in response to osmotic pressure or touch. We used split sfGFP and split Renilla luciferase tags on the C-terminals of both proteins.
</p>
</p>
<p class="lead">
<p class="lead">
-
The split sfGFP is irreversible and was made to show the interaction between our two Pbs2 and Hog1 while we use the reversible split luciferase tags to assess the activation and inactivation of the pathway. In fact, when stress is removed, the signal should decline. The <b>BioTouch Detector </b> is programmed to identify and process the light position and can transmit the information to a computer.
+
The split sfGFP is irreversible and aimed to show the interaction between our two Pbs2 and Hog1 while we used the reversible split luciferase tags to assess the activation and inactivation of the pathway. In fact, when stress is removed, the signal should decline. The BioPad Detector is programmed to identify and process the light position and can transmit the information to a computer.
</p>
</p>
Line 312: Line 310:
<!-- ENGINEERING DETECTOR -->
<!-- ENGINEERING DETECTOR -->
-
The signals induced by the BioTouch Chip are then processed by our self designed detection system: the BioTouch Detector. The BioTouch Detector is mainly made of a cheap computer (Raspberry Pi), a highly sensitive digital camera with appropriate light filters, and a light emitting source. The BioTouch Detector locates signals from various sources (infrared fluorescence, green fluorescence and luminescence), processes them and sends back the relative positions of the signals with respect to the BioTouch Pad. Thanks to this position, we are able to extract information such as giving a computer operating system that the position represents the position of the mouse on a screen, that the well at the given position is a suitable antibiotic candidate, or that a gene of interest has been activated. We therefore effectively control a computer or any other electronic device through a living interface: the BioTouch Pad.
+
The signals induced by the BioPad are then processed by our self designed detection system: the BioPad Detector. The BioPad Detector is mainly made of a cheap computer (Raspberry Pi), a highly sensitive digital camera with appropriate light filters, and a light emitting source. The BioPad Detector locates signals from various sources (infrared fluorescence, green fluorescence and luminescence), processes them and sends back the relative positions of the signals with respect to the BioPad. Thanks to this position, we are able to extract information such as giving a computer operating system that the position represents the position of the mouse on a screen, that the well at the given position is a suitable antibiotic candidate, or that a gene of interest has been activated. We therefore effectively control a computer or any other electronic device through a living interface: the BioPad.
</p>
</p>
 +
<div class="cntr">
 +
<a href="https://static.igem.org/mediawiki/2014/b/bd/IMG_4154.JPG" data-lightbox="raspberry" data-title="the Raspberry Pi with a microfluidic chip on the lens"><img src="https://static.igem.org/mediawiki/2014/8/88/DeviceRasp.png" alt="Device" class="img-border img-responsive" /></a>
 +
<figcaption class="cntr">the Raspberry Pi with a microfluidic chip on the lens</figcaption>
 +
</div>
</div>
</div>

Latest revision as of 03:22, 18 October 2014

Overview

Introduction

Biological responses can be quick and precise! This is the message that our team wants to convey. With this in mind, our team brought forward a novel idea:

Combining Protein Complementation techniques with biosensors and microfluidics allows fast spatiotemporal analysis of bacterial/yeast responses to stimuli.


Our team explored this hypothesis by engineering two stress related pathways in E. coli and S. cerevisiae with in mind the development of a BioPad: a biological touchscreen consisting of a microfluidic chip, touch-responsive bacteria/yeast, and a signal detector. Learn more about how the BioPad works !

The pathway engineered in E. coli, the Cpx Pathway, is a two-component regulatory system responsive to envelope stress. A full description of the pathway is available here.
In S. cerevisiae we modified the HOG Pathway - a MAPKK pathway responsive to osmotic stress. For more information concerning the HOG Pathway click here.





EPFL microfluidic chips

Our project also includes an extensive microfluidics section. Our self designed chips helped us improve precision, safety and quantification methods used throughout the project. To learn more about the microfluidic components of our project check out this link.

first
Raspberry Pi


Last but not least, we designed a novel signal detector! To make signal detection more practical we developed an automatised cheap tracking system made of a mini-computer (Raspberry Pi) and a mini-HD camera. More details concerning the BioPad detector can be found here.




How the BioPad works - E. coli

Potential biopad
A potential BioPad

Our BioPad is a self-designed PDMS microfluidic chip, made of thousands of compartments representing “pixels”. Each 300μm x 300μm x 50μm compartment contains a few layers of E. coli. When the surface of the chip is touched, a deformation on the chip - and thus of the compartments – leads to cellular membrane shear stress and protein aggregation/misfolding in the periplasm.

The histidine kinase sensor CpxA auto-phosphorylates and transfers its phosphate to its corresponding relay protein, CpxR, resulting in its dimerization. We engineered the pathway, by fusing split reporter protein fragments to the CpxR (IFP1.4). This allows the two fragments to remain inactive until physical interaction of CpxR (stimulated by envelope stress) leads to the proper folding of IFP1.4 and reconstitution of its fluorescent properties. As the reconstitution of the split fragments of IFP1.4 are reversible, the system can be shutdown upon stress removal (CpxA changes conformation to become a phosphatase and induces CpxR’s dissociation).

The BioPad also includes a signal detector. This detector is composed of an inexpensive credit card-sized single-board computer called Raspberry Pi, a highly sensitive digital camera with appropriate light filters, and a light-emitting source. It identifies and processes the position of the light/fluorescence emitted by the BioPad. The information about the position of the light relative to chip is then used to control the associated electronic device.



Engineering the HOG pathway in S. cerevisiae


The HOG pathway controls the response to osmotic stress in yeast cells. Like bacteria, our modified S. cerevisiae cells can be loaded into the PDMS microfluidic chips we have designed. Thus cells are confined in small compartments made of a soft material. When the surface of the chip is touched, it leads to a deformation of the chip and its chambers. Since the HOG pathway is reactive to turgor pressure, the mechanical pressure applied activates it. Upon induction of the pathway, which is a classical MAP kinase pathway, PBS2 – a MAPKK – is phosphorylated and binds HOG1 – a MAPK – and in turn phosphorylates it.

Figure of Hog1/Pbs2 split sfGFP and split rLuc

These two kinases were fused to split fluorescent and luminescent proteins, via a 13-amino acid flexible linker, by homologous recombination. This allowed us to detect the phosphorylation of Hog1 by Pbs2 in response to osmotic pressure or touch. We used split sfGFP and split Renilla luciferase tags on the C-terminals of both proteins.

The split sfGFP is irreversible and aimed to show the interaction between our two Pbs2 and Hog1 while we used the reversible split luciferase tags to assess the activation and inactivation of the pathway. In fact, when stress is removed, the signal should decline. The BioPad Detector is programmed to identify and process the light position and can transmit the information to a computer.


The BioPad Detector

The signals induced by the BioPad are then processed by our self designed detection system: the BioPad Detector. The BioPad Detector is mainly made of a cheap computer (Raspberry Pi), a highly sensitive digital camera with appropriate light filters, and a light emitting source. The BioPad Detector locates signals from various sources (infrared fluorescence, green fluorescence and luminescence), processes them and sends back the relative positions of the signals with respect to the BioPad. Thanks to this position, we are able to extract information such as giving a computer operating system that the position represents the position of the mouse on a screen, that the well at the given position is a suitable antibiotic candidate, or that a gene of interest has been activated. We therefore effectively control a computer or any other electronic device through a living interface: the BioPad.

Device
the Raspberry Pi with a microfluidic chip on the lens

Sponsors