Team:Queens Canada/Project/Future
From 2011.igem.org
Line 39: | Line 39: | ||
<h3red> What Can Be Designed in the Future </h3red><p> | <h3red> What Can Be Designed in the Future </h3red><p> | ||
- | <regulartext> The versatility featured by <i>C. elegans</i> as a chassis opens many doors for future genetic engineering endeavors with the worm. The chemotaxis mechanism of <i>C. elegans</i> makes ideas for future projects virtually limitless. The worm could be engineered to move towards the molecule of interest in any circumstance where the location of a point source is not known exactly or is not concentrated in exactly one area. One particularly far-reaching example of this would be engineering the worm to chemotax towards waterborne pathogens. Although it is an ambitious feat to program one living organism to pursue another, the effects, if successful, would be paramount. Proteins on the pathogen’s exterior or even secreted by the pathogen could act as ligands that bind to GPCRs expressed in <i>C. elegans’</i> chemosensory neurons. This would be particularly useful in rural applications | + | <regulartext> The versatility featured by <i>C. elegans</i> as a chassis opens many doors for future genetic engineering endeavors with the worm. The chemotaxis mechanism of <i>C. elegans</i> makes ideas for future projects virtually limitless. The worm could be engineered to move towards the molecule of interest in any circumstance where the location of a point source is not known exactly or is not concentrated in exactly one area. One particularly far-reaching example of this would be engineering the worm to chemotax towards waterborne pathogens. Although it is an ambitious feat to program one living organism to pursue another, the effects, if successful, would be paramount. Proteins on the pathogen’s exterior or even secreted by the pathogen could act as ligands that bind to GPCRs expressed in <i>C. elegans’</i> chemosensory neurons. This would be particularly useful in rural applications due to the risk of pathogen contamination which can affect local agriculture as well as any neighboring wells. To further extend the idea of toxic products leeching into the environment, this bio-remediation could be applied to landfills. We could potentially <i>C. elegans</i> to seek out and neutralize harmful chemicals from batteries or plastics that disturb the surrounding environment. </regulartext><p> |
- | <regulartext>Additionally, <i>C. elegans</i> could be used as a biosensor, again with the added | + | <regulartext>Additionally, <i>C. elegans</i> could be used as a biosensor, again with the added advantage of motility compared to bacteria, such as <i>E. coli</i>. A graded biosensor can be made by having the worm express a different colour based on the concentration of the molecule. This may serve as a way to see where sewage pipes are leaking and the extent of their leakage. Its use as a biosensor may even have agricultural applications. Programming <i>C. elegans</i> to detect certain beneficial minerals or compounds in farming may serve as a way for farmers to assess the quality of their fields better. If a certain compound is limited or present in excess he/she would be able to detect that using <i>C. elegans </i> and adjust his planting routine accordingly. Because <i>C. elegans</i> is non-pathogenic to humans and does not feed on any agricultural products it would be safe to use in this context (provided it had a proper kill switch to prevent an invasive species outbreak). </regulartext><p> |
<regulartext>When working with chemotaxis mechanisms in <i> C. elegans</i> it seems the only limiting factor is finding GPCRs that bind to your target ligand. As a eukaryotic multicellular model organism, GPCRs from a variety of species have a good chance of working well. The ability of human transgenes coding for GPCRs to be successfully expressed in <i>C. elegans</i> would allow for future teams to program the worm to respond to stimuli recognized by human GPCRs. This would likely prove to be a worthwhile endeavor. </regulartext> | <regulartext>When working with chemotaxis mechanisms in <i> C. elegans</i> it seems the only limiting factor is finding GPCRs that bind to your target ligand. As a eukaryotic multicellular model organism, GPCRs from a variety of species have a good chance of working well. The ability of human transgenes coding for GPCRs to be successfully expressed in <i>C. elegans</i> would allow for future teams to program the worm to respond to stimuli recognized by human GPCRs. This would likely prove to be a worthwhile endeavor. </regulartext> |
Revision as of 04:38, 29 September 2011