The goal of this project, over Phase I and Phase II, is to develop and validate a new diagnostic platform for biowarfare detection that provides ultrafast design and implementation. Today, both the scientific and security communities believe that advances in biotechnology have increased the concern for misuse in biological weapon programs. As reports of anthrax attacks across the United States multiplied late last year, an increasing concern grew that new strains with altered genomes may appear. Therefore, new diagnostic technologies that provide quick turnaround assays to previously unknown biowarfare strains are needed. To this end, we developed a novel platform, GENE-CODE 2.0, that provides an ultraquick turn-around to real-time PCR genetic testing. GENE-CODE 2.0 employs an expanded genetic information system (AEGIS) that allows for site-specific enzymatic incorporation of reporter molecules during PCR. The platform has already been demonstrated to the commercial market for ultrasensitive quantitative anthrax detection. In Phase I we will design and demonstrate the platform on CDC Category A biological terror agents. In Phase II we will develop multiplexed systems to analyze multiple genetic sites within a given biowarfare agent with internal assay capabilities that will allow the manufacturer to change sequence specificity in an ultrafast manner.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Business Innovation Research Grants (SBIR) - Phase I (R43)
Project #
1R43AI052898-01
Application #
6555349
Study Section
Special Emphasis Panel (ZRG1-SSS-K (12))
Program Officer
Baker, Phillip J
Project Start
2002-07-15
Project End
2003-01-14
Budget Start
2002-07-15
Budget End
2003-01-14
Support Year
1
Fiscal Year
2002
Total Cost
$105,250
Indirect Cost
Name
Eragen Biosciences, Inc.
Department
Type
DUNS #
City
Madison
State
WI
Country
United States
Zip Code
53717
Sherrill, Christopher B; Marshall, David J; Moser, Michael J et al. (2004) Nucleic acid analysis using an expanded genetic alphabet to quench fluorescence. J Am Chem Soc 126:4550-6