Difference between revisions of "Team:ASIJ Tokyo/CSS"
| Line 212: | Line 212: | ||
<a href="https://2018.igem.org/Team:ASIJ_Tokyo/Safety">SAFETY</a> | <a href="https://2018.igem.org/Team:ASIJ_Tokyo/Safety">SAFETY</a> | ||
</div> | </div> | ||
| + | <div id="content"> | ||
| + | <div id="title"> | ||
| + | <p>A1-AT<br>de<span id="red">LIVER</span>y </p> | ||
| + | <img src="https://static.igem.org/mediawiki/2018/e/ed/T--ASIJ_Tokyo--liverlogocut.png" id="liver"> | ||
| + | </div> | ||
| + | <div id="subtitle"> | ||
| + | <h1> Using Stem Cell and CRISPR Technology to Combat <br> Alpha-1 Antitrypsin Deficiency </h1> | ||
| + | </div> | ||
| + | <div id="abstract"> | ||
| + | <h3> ABSTRACT </h3> | ||
| + | <p> Alpha-1 Antitrypsin deficiency is a common genetic disorder -- the defective gene for which is carried by 1 in 25 people -- which arises from a single base pair mutation in the SERPINA1 gene, resulting in the production of a form of antitrypsin prone to polymerization. The mutated antitrypsin then builds up in liver cells and is unable to inhibit proteases in the lungs, leading to damage in both. Using CRISPR-Cas9 technology, we aimed to fix the error in SERPINA1 so that proper antitrypsin can be produced. We will show proof of concept in E. Coli cells using osmy secretion tags and GFP as a reporter. We hope to design a liver organ bud using IPS cell technology to deliver function A1AT through collaboration with Dr. Kagimoto of Healios Japan KK. | ||
| + | </div> | ||
| + | </div> | ||
<div id="footer-box"> | <div id="footer-box"> | ||
Revision as of 23:45, 19 September 2018
A1-AT
deLIVERy
Using Stem Cell and CRISPR Technology to Combat
Alpha-1 Antitrypsin Deficiency
ABSTRACT
Alpha-1 Antitrypsin deficiency is a common genetic disorder -- the defective gene for which is carried by 1 in 25 people -- which arises from a single base pair mutation in the SERPINA1 gene, resulting in the production of a form of antitrypsin prone to polymerization. The mutated antitrypsin then builds up in liver cells and is unable to inhibit proteases in the lungs, leading to damage in both. Using CRISPR-Cas9 technology, we aimed to fix the error in SERPINA1 so that proper antitrypsin can be produced. We will show proof of concept in E. Coli cells using osmy secretion tags and GFP as a reporter. We hope to design a liver organ bud using IPS cell technology to deliver function A1AT through collaboration with Dr. Kagimoto of Healios Japan KK.
