"
Team:Berkeley Wetlab
From 2009.igem.org
Jennbrophy (Talk | contribs) |
Jennbrophy (Talk | contribs) |
||
| (5 intermediate revisions not shown) | |||
| Line 1: | Line 1: | ||
{{newtemplateBerkeley}}<br> | {{newtemplateBerkeley}}<br> | ||
| - | <center> [[Image:Display-o-matic2.png| | + | <center> [[Image:Display-o-matic2.png|550px]] </center> <br> |
<big><font size="5" face="Book Antiqua"> Abstract</font> </big> <br> | <big><font size="5" face="Book Antiqua"> Abstract</font> </big> <br> | ||
| - | Cell surface display in | + | Cell surface display in ''E. coli'' tethers proteins to the outer membrane in order to localize them to the extracellular environment. While this form of localization has allowed many novel functions to be engineered into ''E. coli'', work within this space relies on a trial and error approach rather than design principles. We worked to create a foundation of research which would make the rational design of cell surface display systems in ''E. coli'' possible. We used a combinatorial approach to compare the ability of different display proteins to display different classes of functional proteins. This required the development and implementation of an automated assembly method able to construct the large number of devices necessary to draw meaningful conclusions about design within this space. |
<br> | <br> | ||
| + | <br> | ||
| + | <br> | ||
| + | <center><font size="5" face="Book Antiqua">Our Team</font></center> <br> | ||
| + | [[Image:BerkeleyWetlabTeam.jpg|center|600px]] | ||
<br> | <br> | ||
<br> | <br> | ||
Latest revision as of 19:14, 21 October 2009
|
Abstract
Cell surface display in E. coli tethers proteins to the outer membrane in order to localize them to the extracellular environment. While this form of localization has allowed many novel functions to be engineered into E. coli, work within this space relies on a trial and error approach rather than design principles. We worked to create a foundation of research which would make the rational design of cell surface display systems in E. coli possible. We used a combinatorial approach to compare the ability of different display proteins to display different classes of functional proteins. This required the development and implementation of an automated assembly method able to construct the large number of devices necessary to draw meaningful conclusions about design within this space.
Acknowledgements
We thank our wonderful advisers: Chris Anderson, Terry Johnson, and Lane Weaver for their guidance and support. We also thank our generous sponsors:
