This proposal concerns the artificially expanded genetic information system (AEGIS), a DNA-like molecular system having 8 letters in addition to the 4 in natural DNA. AEGIS displays five features of a synthetic genetic system (rule-based design, orthogonality, semi-predictable affinity, higher information density, and polymerase incorporability) that permits it to solve a range of problems in medical diagnostics, systems biology, and genomics. Today, over 400,000 patients have their health care improved due to AEGIS -enabled clinical assays that support personalized medicine. This project will move beyond AEGIS as a passive binding system to allow AEGIS components to participate as part of a dynamic system that exploits DNA polymerases and reverse transcriptases. This requires that we develop polymerases that incorporate AEGIS components with very high fidelity and efficiency. To obtain these, DNA polymerase that already do this reasonably well will be placed under selective pressure in a directed evolution experiment. The polymerases that are obtained will then be used in real time PCR instruments to develop nucleotide-polymerase-recipe combinations that support 6-letter polymerase chain reactions. Supporting technology, including the determination of fidelity of incorporation of these. We will then do a demonstration project to show that AEGIS components can solve a difficult problem in modern molecular, systems, and clinical biology: the multiplexing of PCR. Multiplexed PCR is the rate limiting step in many genomics analyses. Our long term, highly ambitious goal is to develop a """"""""synthetic biology"""""""", a chemical system capable of Darwinian evolution, based on AEGIS components. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM081527-02
Application #
7487877
Study Section
Special Emphasis Panel (ZRG1-GGG-J (10))
Program Officer
Portnoy, Matthew
Project Start
2007-08-20
Project End
2011-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
2
Fiscal Year
2008
Total Cost
$265,487
Indirect Cost
Name
Foundation for Applied Molecular Evolutn
Department
Type
DUNS #
134136394
City
Gainesville
State
FL
Country
United States
Zip Code
32604
Benner, Steven A (2012) Aesthetics in synthesis and synthetic biology. Curr Opin Chem Biol 16:581-5
Yang, Zunyi; Chen, Fei; Alvarado, J Brian et al. (2011) Amplification, mutation, and sequencing of a six-letter synthetic genetic system. J Am Chem Soc 133:15105-12
Chen, Fei; Yang, Zunyi; Yan, Maocai et al. (2011) Recognition of an expanded genetic alphabet by type-II restriction endonucleases and their application to analyze polymerase fidelity. Nucleic Acids Res 39:3949-61
Kim, Hyo-Joong; Leal, Nicole A; Benner, Steven A (2009) 2'-deoxy-1-methylpseudocytidine, a stable analog of 2'-deoxy-5-methylisocytidine. Bioorg Med Chem 17:3728-32
Sheng, Pinpin; Yang, Zunyi; Kim, Youngmi et al. (2008) Design of a novel molecular beacon: modification of the stem with artificially genetic alphabet. Chem Commun (Camb) :5128-30