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Team:UT Dallas
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| - | <h2><span><b> | + | <h2><span><b> Immunobots: a step towards intelligent probiotics</b></span></h2> |
| - | <p> | + | <p> Abstract</p> |
| + | <p>The human bowel hosts a rich diversity of symbiotic microflora that provides a powerful engineering platform for intelligent probiotics. These “immunobots” will ideally work in-sync and enhance natural self-repair mechanisms for a range of intestinal diseases associated with tissue damage. Towards this end, we engineered a bacterial chemotaxis pathway that utilizes a chimeric receptor to successfully interface with the immune system. In addition, we introduced an inducible secondary bacterial population that can trigger system-wide self-destruction, conferring an additional level of user control. Each module of our system was characterized using fluorescent reporters and the integrated parts were evaluated by controlled experiments involving wound signal gradients. We envision a probiotic solution that can facilitate localized tissue repair for damage resulting from inflammatory bowel diseases, including ulcerative colitis and Crohn’s disease.</p> | ||
<p class="spec"><a href="https://2011.igem.org/wiki/index.php?title=Team:UT_Dallas/Project" class="rm fl"><font size="4" face="verdana">Read more</a></font></p> | <p class="spec"><a href="https://2011.igem.org/wiki/index.php?title=Team:UT_Dallas/Project" class="rm fl"><font size="4" face="verdana">Read more</a></font></p> | ||
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Revision as of 01:50, 3 September 2011
UTDallas iGem
Immunobots: a step towards intelligent probiotics
Abstract
The human bowel hosts a rich diversity of symbiotic microflora that provides a powerful engineering platform for intelligent probiotics. These “immunobots” will ideally work in-sync and enhance natural self-repair mechanisms for a range of intestinal diseases associated with tissue damage. Towards this end, we engineered a bacterial chemotaxis pathway that utilizes a chimeric receptor to successfully interface with the immune system. In addition, we introduced an inducible secondary bacterial population that can trigger system-wide self-destruction, conferring an additional level of user control. Each module of our system was characterized using fluorescent reporters and the integrated parts were evaluated by controlled experiments involving wound signal gradients. We envision a probiotic solution that can facilitate localized tissue repair for damage resulting from inflammatory bowel diseases, including ulcerative colitis and Crohn’s disease.
