Team:MIT projectContext

UV Toggle

• In 2005, the UT Austin team worked on a light-dependent bacterial printer.

• Kobayashi, Collins, et al. "Programmable cells: Interfacing natural and engineered gene networks". PNAS. 2004.
• Crowl, et al. "Repressor cleavage as a prophage induction mechanism: Hypersensitivity of a mutant λ cI protein to RecA-mediated proteolysis". J Mol Bio. 1981.
• Gimble and Sauer. "Mutations in Bacteriophage X Repressor That Prevent RecA-Mediated Cleavage". Journal of Bacteriology. 1985.

Phage

• In 2006 the McGill team attempted to use leucine zippers fused to split YFP to display on cells and cause the cells to adhere via the split YFP. See: http://parts.mit.edu/wiki/index.php/McGill_University_2006



• The 2009 Freiburg Bioware team used Fos/Jun for a 'programmable enzyme' using Fok-fused Fos/Jun as factor in DNA cleavage. See: https://2009.igem.org/Team:Freiburg_bioware/Project/FOS



• Paris's team in 2009 attempted to use Jun/Fos as a snare; Jun on signal vesicle, Fos on membrane of receiving cell. See: https://2009.igem.org/Team:Paris#top



• This year, Duke's team is using Jun- and Fos-based synthetic leucine zippers for genetic regulation. See: https://2010.igem.org/Team:Duke/Project#Leucine_Zippers

• Rackonjac and Model. "Roles of pIII is Filamentous Phage Assembly". J Mol Bio. 1998.
• Barbas III, et al. "Phage Display: A Laboratory Manual". CSH Press. 2001.
• Wang, et al. "Adapter-directed display: a modular design for shuttling display on phage surfaces". J Mol Bio. 2010.
• Smith and Petrenko. "Phage Display". Chemical Review. 1997.
• Sweeney, et al. "Assembly of Multimeric Phage Nanostructures Through Leucine Zipper Interactions". Biotechnology and Bioengineering. 2006.
• Roth, et al. "A Minimized M13 Coat Protein Defines the Requirements for Assembly into the Bacteriophage Particle". J Mol Bio. 2002.
• Weiss and Sidhu. "Design and Evolution of Artificial M13 Coat Proteins". J Mol Bio. 2000.