Team:Brasil-SP/Project

From 2014.igem.org

(Difference between revisions)
 
(7 intermediate revisions not shown)
Line 1: Line 1:
-
<!-- *** What falls between these lines is the Alert Box!  You can remove it from your pages once you have read and understood the alert *** -->
+
{{:Team:Brasil-SP/Templates/Header|headersrc=TheProjectBRASILSP.png}}
-
 
+
-
 
+
-
{{:Team:Brasil-SP/Templates/Header}}
+
<html>
<html>
-
<!--main content -->
 
-
<table width="70%" align="center">
 
-
 
-
 
-
</tr>
 
-
</tr>
 
-
</td>
 
-
 
-
<tr> <td colspan="3"  height="15px"> </td></tr>
 
-
<tr><td bgColor="#e7e7e7" colspan="3" height="1px"> </tr>
 
-
<tr> <td colspan="3"  height="5px"> </td></tr>
 
<tr>
<tr>
Line 24: Line 10:
<tr>
<tr>
<td colspan="3"><h3 align="center">Project Description</h3>
<td colspan="3"><h3 align="center">Project Description</h3>
-
<p><div align="justify">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Our project consists of a biological molecular device (using <i>Bacillus subtilis</i> as chassis) for detection of Cystatin C, a biomarker of chronic kidney disease. The genetic circuit being assembled is based on the outstanding project of the Imperial College of London team of iGEM 2010 (special thanks to the ex-iGEMer Christopher Hirst, who helped us a lot sending some important BioBricks). Part of our mission is also to improve the characterization of the BioBricks developed on 2010 and to validate the molecular design as a generic detection system. This flexibility of detection is based on a protease cleavage of a membrane protein who triggers the genetic circuit (Detection Module). Since any cleavage site could be designed, virtually any protease could be used as a signal for the detection. The cleavage of the linker will trigger a cellular signaling cascade. This signal will then be processed by the Diagnosis Module and finally the result will be displayed by the Response Module. We are on the way to assemble all the parts and properly characterize each part of our construction on time for the Jamboree.</p>
+
<p><div align="justify">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Our project consists of a biological molecular device for detection of early stage chronic kidney disease using Cystatin C as biomarker and <i>Bacillus subtilis</i> as chassis. The genetic circuit being assembled is based on the outstanding project of <a href="https://2010.igem.org/Team:Imperial_College_London#">iGEM 2010 Imperial College of London team </a> (special thanks to the ex-iGEMer Christopher Hirst, who helped us a lot sending some important BioBricks). Part of our mission is also to improve characterization of the BioBricks developed in 2010 and to validate the molecular design as Cystatin C detection system. This flexibility of detection is based on a protease cleavage of a membrane protein which triggers the genetic circuit. Since any cleavage site could be designed, virtually any protease could be used as a signal for the detection. In our case, the disease biomarker will inhibit the action of Cathepsin S protease and the detection will be made indirectly and negatively - <i>i.e.</i> by the Cathepsin lack of protease activity and absense of the system output. We are on the way to assemble all the parts and properly characterize each part of our construction on time for the Jamboree. After completion we'll integrate the full circuit in <em>Bacillus subtilis</em>.<br>  
<br>
<br>
<br>
<br>
Line 38: Line 24:
-
<br><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Because our team has three universities located in different cities the project itself is being developted in separated locations. The parts are listed bellow.</p></div>
+
<br><p>&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;Because our team involves three universities located in different cities, the project itself is being developted in separated locations. The parts of the project are listed bellow.</p></div>
</td>
</td>
</tr>
</tr>
Line 47: Line 33:
-
 
-
 
-
<!--<tr>
 
-
<td colspan="3"><h3 align="center">Overview</h3>
 
-
<p><div align="justify">&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;In 2012, a census conducted by the Brazilian Nephrology Society estimated that 97,500 patients are under dialysis treatment per year. This number demands around 1.4 billion reals annually from the Brazilian Federal Government, corresponding to approximately 10% of public budget addressed to health in the country. The earlier the diagnosis, the bigger are the chances of a successful kidney disease treatment. However, the methods commonly used are only detecting renal dysfunction in late stages, and on top of, some kidney diseases, such as Chronic Kidney Disease, are asymptomatic. Together, this two facts hamper the early diagnosis and the development of an appropriate treatment.</div></p>
 
-
</td>
 
-
</tr>-->
 
-
<br>
 
-
<h3>References </h3>
 
-
<p>
 
-
iGEM teams are encouraged to record references you use during the course of your research. They should be posted somewhere on your wiki so that judges and other visitors can see how you though about your project and what works inspired you. </p>
 
</td>
</td>

Latest revision as of 00:00, 18 October 2014

TheProjectBRASILSP.png


Project Description

     Our project consists of a biological molecular device for detection of early stage chronic kidney disease using Cystatin C as biomarker and Bacillus subtilis as chassis. The genetic circuit being assembled is based on the outstanding project of iGEM 2010 Imperial College of London team (special thanks to the ex-iGEMer Christopher Hirst, who helped us a lot sending some important BioBricks). Part of our mission is also to improve characterization of the BioBricks developed in 2010 and to validate the molecular design as Cystatin C detection system. This flexibility of detection is based on a protease cleavage of a membrane protein which triggers the genetic circuit. Since any cleavage site could be designed, virtually any protease could be used as a signal for the detection. In our case, the disease biomarker will inhibit the action of Cathepsin S protease and the detection will be made indirectly and negatively - i.e. by the Cathepsin lack of protease activity and absense of the system output. We are on the way to assemble all the parts and properly characterize each part of our construction on time for the Jamboree. After completion we'll integrate the full circuit in Bacillus subtilis.






     To address a real world situation, we are working on the same principle and aesthetics of the well known devices for biodetection like pregnancy or HIV tests: easy-to-use microfluidic devices. The plan is to design a microchip able to store spores of the developed strains of B. subtilis and safely expose blood samples to our biodetection system, successfully containing the biomaterial and enabling a proper discard of the chip. A priori, the device output monitoring would require a fluorescence detector tool, but we also propose a naked eye output observation as a concept for future prospects.


     Since we are working on a solution for a problem directly related to ordinary people, having a public feedback about synthetic biology is very important to analyze the social impact of our work and it help us to evaluate the biosafety and bioethical issues beyond a simple risk analysis - a sociological characterization of the values of our project. Thus, as a policy and practices approach, we will try to report public opinion of Brazil on these issues using a questionnaire to evaluate our actual scenario and, in a certain way, our own project.


     Because our team involves three universities located in different cities, the project itself is being developted in separated locations. The parts of the project are listed bellow.