Team:Washington/Accomplishments

From 2009.igem.org

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='''Accomplished'''=
='''Accomplished'''=
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*Demonstrated that at least one new BioBrick Part of our own design and construction works as expected.
 
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**Protein Expression Vector (LINK TO REGISTRY & WIKI SITE)
 
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**Target Expression Vector (LINK TO REGISTRY & WIKI SITE)
 
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**OpdA, a nerve agent degrading enzyme (LINK TO REGISTRY & WIKI SITE)
 
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*Characterized an existing BioBrick Part and entered the information back on the Registry. [https://2009.igem.org/Team:Washington/Project/]
 
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**[http://partsregistry.org/wiki/index.php/Part:BBa_J36848 BBa_J36848]
 
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**[http://partsregistry.org/wiki/index.php/Part:BBa_J36849 BBa_J36849]
 
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**[http://partsregistry.org/wiki/index.php/Part:BBa_J36850 BBa_J36850]
 
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**[http://partsregistry.org/wiki/index.php/Part:BBa_J36851 BBa_J36851]
 
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*Synthesize and BioBrick type I secretion system from Erwinia Chrysanthemi
 
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**[http://partsregistry.org/wiki/index.php/Part:BBa_K215107 BBa_K215107], prtDEF from Erwinia Chrysanthemi under constitutive expression in low copy plasmid STRONG PROMOTER
 
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**[http://partsregistry.org/wiki/index.php/Part:BBa_K215107 BBa_K215107], prtDEF from Erwinia Chrysanthemi under constitutive expression in low copy plasmid MEDIUM PROMOTER
 
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**[http://partsregistry.org/wiki/index.php/Part:BBa_K215107 BBa_K215107], prtDEF from Erwinia Chrysanthemi under constitutive expression in low copy plasmid WEAK PROMOTER
 
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*Develop assay for looking for secreted proteins
 
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**[https://2009.igem.org/Team:Washington/Project/Secretion]See Project Page: Secretion
 
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*Develop new modular surface display system
 
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*Computationally design novel Biotin-binding protein using Rosetta
 
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*Gain real-world synthetic biology experience
 
 +
=== Demonstrated that at least one new BioBrick Part of our own design and construction works as expected ===
 +
*Protein Expression Vector (LINK TO REGISTRY & WIKI SITE)
 +
*Target Expression Vector (LINK TO REGISTRY & WIKI SITE)
 +
*OpdA, a nerve agent degrading enzyme (LINK TO REGISTRY & WIKI SITE)
 +
 +
=== Characterized an existing BioBrick Part and entered the information back on the Registry. [https://2009.igem.org/Team:Washington/Project/] ===
 +
*[http://partsregistry.org/wiki/index.php/Part:BBa_J36848 BBa_J36848]
 +
*[http://partsregistry.org/wiki/index.php/Part:BBa_J36849 BBa_J36849]
 +
*[http://partsregistry.org/wiki/index.php/Part:BBa_J36850 BBa_J36850]
 +
*[http://partsregistry.org/wiki/index.php/Part:BBa_J36851 BBa_J36851]
 +
 +
=== Synthesize and BioBrick type I secretion system from Erwinia Chrysanthemi ===
 +
*[http://partsregistry.org/wiki/index.php/Part:BBa_K215107 BBa_K215107], prtDEF from Erwinia Chrysanthemi under constitutive expression in low copy plasmid STRONG PROMOTER
 +
*[http://partsregistry.org/wiki/index.php/Part:BBa_K215107 BBa_K215107], prtDEF from Erwinia Chrysanthemi under constitutive expression in low copy plasmid MEDIUM PROMOTER
 +
*[http://partsregistry.org/wiki/index.php/Part:BBa_K215107 BBa_K215107], prtDEF from Erwinia Chrysanthemi under constitutive expression in low copy plasmid WEAK PROMOTER
 +
 +
=== Develop assay for looking for secreted proteins ===
 +
*[https://2009.igem.org/Team:Washington/Project/Secretion]See Project Page: Secretion
 +
 +
=== Develop new modular surface display system ===
 +
 +
=== Computationally design novel Biotin-binding protein using Rosetta ===
 +
 +
=== Gain real-world synthetic biology experience ===
='''BioBricks'''=
='''BioBricks'''=

Revision as of 20:21, 18 October 2009

Uw title logo.png



Accomplished

Demonstrated that at least one new BioBrick Part of our own design and construction works as expected

  • Protein Expression Vector (LINK TO REGISTRY & WIKI SITE)
  • Target Expression Vector (LINK TO REGISTRY & WIKI SITE)
  • OpdA, a nerve agent degrading enzyme (LINK TO REGISTRY & WIKI SITE)

Characterized an existing BioBrick Part and entered the information back on the Registry. [1]

Synthesize and BioBrick type I secretion system from Erwinia Chrysanthemi

  • BBa_K215107, prtDEF from Erwinia Chrysanthemi under constitutive expression in low copy plasmid STRONG PROMOTER
  • BBa_K215107, prtDEF from Erwinia Chrysanthemi under constitutive expression in low copy plasmid MEDIUM PROMOTER
  • BBa_K215107, prtDEF from Erwinia Chrysanthemi under constitutive expression in low copy plasmid WEAK PROMOTER

Develop assay for looking for secreted proteins

  • [2]See Project Page: Secretion

Develop new modular surface display system

Computationally design novel Biotin-binding protein using Rosetta

Gain real-world synthetic biology experience

BioBricks

Target Vector

Target structure.png

BBa_K215002 Is a BioBrick part that was made to work in conjunction with the Secretion System (BBa_K215107). When used it creates a fusion protein, that contains the prtB secretion signal recognized by the secretion system. It also fuses to the protein a nano-tag that is able to bind Streptavidin, TEV protease site (for isolating your protein from the fusion) and Histidine Epitote Tags for easy protein purification.

  • Current Status: Complete





Secretion System



Secretion structure.png

BBa_K215107 Is a BioBrick version of the Type 1 secretion system of Erwinia Chrysanthemi. It secretes proteins that contain the prtB C-terminus Epitote tag. To create a fusion protein with the prtB tag see BBa_K215002.

  • Current Status: In progress





Display System



Display structure.png

BBa_K215200 is a Display vector that will allow for the presentation of any protein onto the surface of a cell by fusing the protein to Outer Membrane Protein A (OMPA). The fusion protein contains a GS peptide linker to space the displayed protein away from the outer membrane and also contains a TEV protease site to allow for purification of the displayed protein.

  • This Part is composed of:
    • BBa_K215201: Display Vector with 5 trans-membrane OMPA
    • BBa_K215250: Coding Sequence for fusion protein scaffold, 1 trans-membrane OMPA
    • BBa_K215251: Coding Sequence for fusion protein scaffold, 5 trans-membrane OMPA


  • Current Status: In progress





Quick overview of what was done and the status of everyting. Maybe 3 paragraphs (display, secretion, conclusions)