Team:Washington/Accomplishments

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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)