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Team:Berkeley Wetlab/Project Overview
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We made passengers representative of the major types of protiens/peptides people have tried to display in the past. Made many display systems in a combinatorial fashion to come up stemployed a combinatorial method, testing many variations of display and spacers for each passenger, in order to come . Because this requires the construction of a very large number of parts, we developed a high throughput automated assembly method. The data generated by this method allows future investigators to estimate the number of combinations that must be constructed in order to find functional display, and helps investigators chose subsets of combinations within the design space that are most likely to yield success. | We made passengers representative of the major types of protiens/peptides people have tried to display in the past. Made many display systems in a combinatorial fashion to come up stemployed a combinatorial method, testing many variations of display and spacers for each passenger, in order to come . Because this requires the construction of a very large number of parts, we developed a high throughput automated assembly method. The data generated by this method allows future investigators to estimate the number of combinations that must be constructed in order to find functional display, and helps investigators chose subsets of combinations within the design space that are most likely to yield success. | ||
=====Passengers===== | =====Passengers===== | ||
| - | * | + | * Typically passengers are proteins/peptides that would not naturally reside on the outermembrane of E.coli, but are put there by a cell surface display device. They are the functional units of cell surface display devices. We chose to examine passengers that would be essential to display for bacterial systems of interesting application. We also chose passengers whose functional display could be assayed in vivo and high throughput. To read more about the passengers we used and our success in dispalying them, visit our [[Team:Berkeley_Wetlab/Assay_Protocols | parts]] page. |
=====Displayers===== | =====Displayers===== | ||
Revision as of 19:44, 19 October 2009
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Contents |
What is Cell Surface Display?
Cell surface display is a system for exposing proteins/peptides to the extracellular environment by anchoring them to the outermembrane of a cell. This is done by fusing a protein or peptide of interest to a protein domain that naturally inserts itself into the outer membrane. Genetic devices for cell surface display are generally composed of three basic components:
- Passenger domain: the protein or peptide exposed to the extracellular environment.
- Displayer domain: the domain that anchors the passenger to the outer membrane.
- Structural Spacer Element: a link between the passenger and the displayer.
The Problem
Certain functions cannot be engineered into E. coli without a cell surface display system. However, success in building a functional cell surface display system currently relies on a trial and error approach that is not guided by design principles. While it is almost certain that for a given passenger, a combination of displayer and structural spacers exists that leads to functional display, it is not clear what this combination is or how to chose such a combination rationally.
Our Goal
To create basic design principles for cell surface display which can serve as guidelines for future iGEM teams (and others) attempting to build systems that involve cell surface display.
Our Approach
We made passengers representative of the major types of protiens/peptides people have tried to display in the past. Made many display systems in a combinatorial fashion to come up stemployed a combinatorial method, testing many variations of display and spacers for each passenger, in order to come . Because this requires the construction of a very large number of parts, we developed a high throughput automated assembly method. The data generated by this method allows future investigators to estimate the number of combinations that must be constructed in order to find functional display, and helps investigators chose subsets of combinations within the design space that are most likely to yield success.
Passengers
- Typically passengers are proteins/peptides that would not naturally reside on the outermembrane of E.coli, but are put there by a cell surface display device. They are the functional units of cell surface display devices. We chose to examine passengers that would be essential to display for bacterial systems of interesting application. We also chose passengers whose functional display could be assayed in vivo and high throughput. To read more about the passengers we used and our success in dispalying them, visit our parts page.
Displayers
- Displayers can be divided into two classes, N terminal and C terminal, based on which terminus of the displayer its passenger is fused to. We built cell surface display systems using many different N and C terminal displayers. Most of the displayers we examined were autotransporters, proteins that form a pore in the outermembrane and then pull their N terminus through this pore, but many were common outermembrane proteins that have exposed extracellular termini. To read more about the displayers we used, visit our parts page.
Spacers
- Structural spacer regions are common in natural display systems. However, their function is unclear, so most people engineer cell surface display devices without spacer regions. We decided to examine the effect that spacer elements have on engineered cell surface display devices. To read more about the spacer parts we built visit our parts page.
