IGEM:Stanford/2009/GCPR: Difference between revisions

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==Papers==
==Papers==
*Genetic analysis of G protein-coupled receptor expression in Escherichia coli: Inhibitory role of DnaJ on the membrane integration of the human central cannabinoid receptor," article from Biotechnology and Bioengineering http://www3.interscience.wiley.com/search/allsearch?mode=viewselected&product=journal&ID=121385939&view_selected.x=100&view_selected.y=6&view_selected=view_selected
*Troubleshooting??  Genetic analysis of G protein-coupled receptor expression in Escherichia coli: Inhibitory role of DnaJ on the membrane integration of the human central cannabinoid receptor," article from Biotechnology and Bioengineering http://www3.interscience.wiley.com/search/allsearch?mode=viewselected&product=journal&ID=121385939&view_selected.x=100&view_selected.y=6&view_selected=view_selected
*"Efficient production of membrane-integrated and detergent-soluble G protein-coupled receptors in Escherichia coli," article from Protein Science, 2008: http://www.ncbi.nlm.nih.gov/pubmed/18593817
*"Efficient production of membrane-integrated and detergent-soluble G protein-coupled receptors in Escherichia coli," article from Protein Science, 2008: http://www.ncbi.nlm.nih.gov/pubmed/18593817
**Article that discusses some of the complications that emerge when expressing GPCRs in microbial systems.  One of the solutions this group found was co-expression of the GPCR-GFP construct with various regulatory proteins involved in membrane metabolism.  Coexpression with the AAA+ protease FtsH, an enzyme involvedin MP degradation and quality control. (Article to be read in advance of Monday's meeting)
**Article that discusses some of the complications that emerge when expressing GPCRs in microbial systems.  One of the solutions this group found was co-expression of the GPCR-GFP construct with various regulatory proteins involved in membrane metabolism.  Coexpression with the AAA+ protease FtsH, an enzyme involvedin MP degradation and quality control. (Article to be read in advance of Monday's meeting)
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*[http://www.ncbi.nlm.nih.gov/pubmed/15251227 Bible] of GPCR mechanisms.
*[http://www.ncbi.nlm.nih.gov/pubmed/15251227 Bible] of GPCR mechanisms.
*[http://peds.oxfordjournals.org/cgi/reprint/19/1/1 GPCR Engineered in Yeast]
*[http://peds.oxfordjournals.org/cgi/reprint/19/1/1 GPCR Engineered in Yeast]
*The grad students in CSB 220 heard about these modified GPCRs known as RASSL (receptors adapted to synthetic ligands). May be the techniques we are looking for. [http://www.pnas.org/content/104/12/4777.full Review]. [http://www.nature.com/nmeth/journal/v5/n8/abs/nmeth.1232.html Methods]. It doesn't seem as if this technique seems to have expanded to synbio.


==Meeting Notes==
==Meeting Notes==

Latest revision as of 23:33, 24 June 2009

Summary

Comments and Discussion

  • Can we identify a specific GPCR or class of GPCRs that we are interested in manipulating?
  • Which host organism would make the best chassis?
  • What should our GPCR be sensitive to?

Papers

Meeting Notes

  • 5/4 Small Group
    • Methods/Procedures we should familiarize ourselves with: FACS, SDS-PAGE, Western-Blotting, iron-affinity chromatography
    • The paper underscored the difficulty of expressing functional GPCRs in E. coli. Can we find other papers that have troubleshooted this? Or perhaps should we designate a sub-group to examine the activity/functionality of our GPCR while the bulk of the team works on co-expressing two GPCRs in E. coli?
    • Should we consider yeast as our chassis? What are the tradeoffs? What has been done to express GPCRs in yeast?
    • Is there necessarily a trade-off between activity and modularity? (i.e. Will the time constraint limit us to either pursuing a functional GPCR or a modular and expressed but dysfunctional GPCR plasmid?)

Questions

  • I would highly recommend looking through George Georgiou's literature to see what engineered parts he has made. - Chris
  • Thanks for the suggestion; the article for Monday's meeting is by Georgiou. Any other recommendations?