Difference between revisions of "Applications of Ribozymes in Synthetic Systems - Danielle Jordan"
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== Ribozymes in Synthetic Systems == | == Ribozymes in Synthetic Systems == | ||
=== [[Nanocircles]] === | === [[Nanocircles]] === | ||
| − | [http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11752404&dopt=AbstractPlus Efficient bacterial transcription of DNA nanocircle vectors with optimized single-stranded promoters] Ohmichi ''et al.'' | + | [http://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11752404&dopt=AbstractPlus Efficient bacterial transcription of DNA nanocircle vectors with optimized single-stranded promoters] Ohmichi ''et al.'' 2001. |
=== [[Ribozyme Switch]] === | === [[Ribozyme Switch]] === | ||
| − | [http://www.pnas.org/cgi/content/abstract/104/36/14283 A modular and extensible RNA-based gene-regulatory platform for engineering cellular function] Win and Smolke. | + | [http://www.pnas.org/cgi/content/abstract/104/36/14283 A modular and extensible RNA-based gene-regulatory platform for engineering cellular function] Win and Smolke. 2007. |
=== [[Ribozyme vesicles]] === | === [[Ribozyme vesicles]] === | ||
Revision as of 16:21, 20 November 2007
Contents
History and Background
What are ribozymes?
Ribozymes, also known as RNA enzymes or catalytic RNA, are RNA molecules that cataylze chemical reactions. They are able to catalzye hydrolysis of their own phosphodiester bonds or other RNA bonds. Some, such as RNA polymerase ribozymes, are able to catalyze their own synthesis.
How do you make artificial ribozymes?
The method of directed evolution is used to create specific ribozymes. Large quantities of RNA are produced using polymerase enzymes. The large library of ribozymes are mutated and amplified using error prone rtPCR (reverse transcriptase PCR). One method of selection is by using biotin tags, which are covalently bonded to a particular substrate and can then be extracted by streptavidin-magnetic beads. Thus, the molecules that exhibit the optimal ligase activity are recoved using the streptavidin matrix.
Why are they being used?
Current protein promoters cannot easily be transferred from prokaryotic to eukaryotic organisms. However, ribozymes can be used in both systems because ribozymes do not rely on the cell's genetic information. Also, ribozymes can be artifically selected to respond to any set of exogenous molecules whereas there are only a limited number of protein promoters. Lastly, ribozymes can be transported into the cell to affect gene regulatory function whereas protein promoters have to be integrated into the DNA. Ribozymes will not naturally stay permanently in a cell but rather be transported out of the cell or diluted over time.
Ribozymes in Synthetic Systems
Nanocircles
Efficient bacterial transcription of DNA nanocircle vectors with optimized single-stranded promoters Ohmichi et al. 2001.
Ribozyme Switch
A modular and extensible RNA-based gene-regulatory platform for engineering cellular function Win and Smolke. 2007.
Ribozyme vesicles
RNA Catalysis in Model Protocell Vesicles Chen et al. 2005
References
Chen IA, Salehi-Ashtiani K, Szostak JW (2005). RNA Catalysis in Model Protocell Vesicles. Journal of the American Chemical Society 127(38):13213-9.
Lindstrom UM, Chandrasekaran RA, Orbai L, Helquist SA, Miller GP, Oroudjev E, Hansma HG, Kool ET (2002). Artificial human telomeres from DNA nanocircle templates. PNAS 99(25):15953-8. Epub 2002 Nov 20. Abstract
Ohmichi T, Maki A, Kool ET (2001). Efficient bacterial transcription of DNA nanocircle vectors with optimized single-stranded promoters. PNAS 99(1):54-9. Epub 2001 Dec 18. Abstract.
Win MN, Smolke CD (2007). A modular and extensible RNA-based gene-regulatory platform for engineering cellular function. PNAS 104(36):14283-8. Epub 2007 Aug 20. Abstract.
