Difference between revisions of "Team:BioIQS-Barcelona/Description"

 
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                     <div class="header-content">
 
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                         <h1 class="mb-5">Project | Overview</h1>
 
                         <h1 class="mb-5">Project | Overview</h1>
                         <a href="https://2018.igem.org/Team:BioIQS-Barcelona/Description#download" class="btn btn-outline btn-xl js-scroll-trigger">Have a look!</a>
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                         <a href="https://2018.igem.org/Team:BioIQS-Barcelona/Description#cl-description" class="btn btn-outline btn-xl js-scroll-trigger">Have a look!</a>
 
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                     <h2 class="section-heading orange">Project description</h2>
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                    <h3 class="orange">We would like to present you a brief description of our project on celiac disease:</h3>
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                        <h2 class="section-heading orange">Human Practices</h2>
 
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                        <p class="book orange">Our project is based on the design of a <b>personalized gluten sensor</b> by using the common tools of synthetic biology. There are already several sensors that are able to detect gluten in the food. However, there are milestones that still have not been overcome. We propose a robust model in which the HLA molecule of a patient is expressed and used as a sensor to detect specific reactive gluten epitopes.</p>
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                                    <p class="book orange-medium">Our project aims to offer a real-world solution to ease celiac patient's life. Consequently, we engaged with the celiac community in an integrative way. See how <a href="https://2018.igem.org/Team:BioIQS-Barcelona/Human_Practices">the necessities of the celiac community</a> shaped our project.</p>
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                    <a class="js-scroll-trigger a-arrow" href="https://2018.igem.org/Team:BioIQS-Barcelona/Description#t-project"><span class="arrow down"></span></a>
 
 
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                    <img src="https://static.igem.org/mediawiki/2018/2/26/T--BioIQS-Barcelona--2018_t-cell.png">
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                        <h2 class="section-heading white" style="/*Activar per tallar paraula massa llarga overflow-wrap: break-word; word-wrap: break-word;*/ overflow: hidden; word-break:break-all; /*Activar per ficar 3 puntets white-space: nowrap; text-overflow: ellipsis*/;">PCR standardization</h2>
                             <p class="text-b"><b>Coeliac disease (CD)</b> is an autoimmune disorder that is closely related with HLA (Human leukocyte antigen), a type of receptor that are located in the surface of almost every cell of a human tissue, including white blood cells.</p>
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                                    <p class="book white">The personalized gluten sensor is based on the same molecule used by the human immune system cells to detect the presence of gluten, the <a href="https://2018.igem.org/Team:BioIQS-Barcelona/Celiac_disease.thml">HLA-DQ protein</a>. </p>
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                                    <p class="book white">Different variants of this protein detect different gluten epitopes. Therefore, the sensor can be personalized if it incorporates the genetic variant of the HLA-DQ protein of each patient. However, personalization often comes at a higher cost. Our team designed and characterized a <a href="https://2018.igem.org/Team:BioIQS-Barcelona/Basic_Part">standard PCR protocol</a> that could be used to obtain the genetic variant of each user to make the personalization of the sensor feasible.</p>
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                    <p class="apart fletxa">These molecules are responsible for the correct discrimination between what is self and foreign proteins, guaranteeing the correct immune response against foreign agents that can cause infections.
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                        Within the HLA protein family there are the highly polymorphic HLA-DQ, which means that
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                         <b>there are a lot of existing genetic variants of these molecules</b>. Some of these HLA-DQ variants are able to recognize different gluten epitopes (aminoacid sequence of a protein) and present them to the T cells. More specifically, 25% of the general population carry the HLA-DQ that can recognize gluten derived epitopes, but only 1% of the population suffer from coeliac disease.
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                    </p>
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                                <h2 class="section-heading orange">Expression system</h2>
 
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                    <p class="apart yellow">The reason of such fact is that the inflammatory reaction is triggered by some T cells that can sense the gluten epitope presented by the HLA-DQ.</p>
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                    <!--                    <img src="styles/img/hla-solo.png">-->
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                                    <p class="book orange-medium">Since our sensor is based on a human protein, the expression system of it needs to be thoroughly designed. Our team carefully studied different approaches to make possible the HLA-DQ protein expression in <i>E. coli</i>. Additionally, other expression hosts that can carry post-transductional modifications, such as <i>P. pastoris</i>, have been also considered.</p>
 
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                                    <p class="book orange-medium">We have tested and characterized these expression systems to choose which one would be used to create our sensor. See more in our <a href="https://2018.igem.org/Team:BioIQS-Barcelona/Composite_Part">composite parts</a> page.</p>
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                            <p class="text-b">Understanding why the inflammatory response is triggered by a certain type of T cells upon epitope presentation by HLA-DQ molecules is essential to uncover the mechanism of CD. Since the first step for the immune response activation is the recognition and binding of the gluten epitope to the HLA-DQ receptor. </p>
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                    <p class="apart yellow">The development of a personalized sensor to determine reactive epitopes could help to better understand the disease and would also allow the screening of those foods that could potentially trigger an immune response to the patient.</p>
 
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                    <a href="https://2018.igem.org/Team:BioIQS-Barcelona/Description#objectiv" class="text-transform js-scroll-trigger">Look our objectives!</a>
 
 
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                     <h2 class="section-heading orange">Objectives</h2>
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                    <h3 class="orange">Here there are:</h3>
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                                <h2 class="section-heading white">Detection system</h2>
                        <p class="book">In our iGEM Project we will design a
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                            <b>personalized gluten sensor</b> through a synthetic biology approach. To do so, we decided to build a model based on the HLA expression of the patient which will be coupled to a sensor, allowing the detection of reactive epitopes. The main specificities of our sensor are described as follows:</p>
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                                    <p class="book white">We believe in the inner beauty of every project. Therefore, we are aware that the experimental work is essential, but nothing could be developed without a solid model. Our team designed a theoretical model of the sensor, which studies the detection system of our sensor. See more in our <a href="https://2018.igem.org/Team:BioIQS-Barcelona/Model">modeling page</a>.</p>
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                    <a class="js-scroll-trigger a-arrow" href="https://2018.igem.org/Team:BioIQS-Barcelona/Description#t-objectives"><span class="arrow down"></span></a>
 
 
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                             <p class="apart big">first</p>
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                                    <p class="text-b">Since our sensor will be built <b>according to the patient HLA</b>, it will allow the detection of specific reactive epitopes independently of the food source.</p>
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                                <h2 class="section-heading orange" id="cuttheword">Collaborations</h2>
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                                    <p class="book orange-medium">One of the most exciting things of being part of the iGEM community is the possibility to build relations with other teams from all around the world. When it comes to research, it is essential to establish collaborations. In the iGEM competition, there are several ways to share, communicate and set up a network with the community. See how we engaged with other teams in our <a href="https://2018.igem.org/Team:BioIQS-Barcelona/Collaborations">collaborations page</a>.</p>
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                            <p class="apart big">second</p>
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                            <p class="text-b">Additionally, our sensor will be able to detect reactive epitopes even in
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                                <b>fermented foods.</b></p>
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                        <p class="apart big">third</p>
 
                        <p class="text-b">The methodology implemented in our sensor could be used for the <b>identification of new reactive epitopes</b> and unknown allelic variants.</p>
 
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                    <p class="apart big">fourth</p>
 
                    <p class="text-b">Our design requires<b> only a DNA sample of the patient.</b> Therefore, the methodology and application of our sensor could be extended for the detection of other HLA related disorders.</p>
 
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Latest revision as of 18:56, 17 December 2018

BIO IQS

Project | Overview

Have a look!

Human Practices

Our project aims to offer a real-world solution to ease celiac patient's life. Consequently, we engaged with the celiac community in an integrative way. See how the necessities of the celiac community shaped our project.

PCR standardization

The personalized gluten sensor is based on the same molecule used by the human immune system cells to detect the presence of gluten, the HLA-DQ protein.

Different variants of this protein detect different gluten epitopes. Therefore, the sensor can be personalized if it incorporates the genetic variant of the HLA-DQ protein of each patient. However, personalization often comes at a higher cost. Our team designed and characterized a standard PCR protocol that could be used to obtain the genetic variant of each user to make the personalization of the sensor feasible.

Expression system

Since our sensor is based on a human protein, the expression system of it needs to be thoroughly designed. Our team carefully studied different approaches to make possible the HLA-DQ protein expression in E. coli. Additionally, other expression hosts that can carry post-transductional modifications, such as P. pastoris, have been also considered.

We have tested and characterized these expression systems to choose which one would be used to create our sensor. See more in our composite parts page.

Detection system

We believe in the inner beauty of every project. Therefore, we are aware that the experimental work is essential, but nothing could be developed without a solid model. Our team designed a theoretical model of the sensor, which studies the detection system of our sensor. See more in our modeling page.

Collaborations

One of the most exciting things of being part of the iGEM community is the possibility to build relations with other teams from all around the world. When it comes to research, it is essential to establish collaborations. In the iGEM competition, there are several ways to share, communicate and set up a network with the community. See how we engaged with other teams in our collaborations page.