Real-Time Heteroplasmy Analysis on Microarrays

Award Information
Agency: Department of Health and Human Services
Branch: N/A
Contract: 1R44GM084603-01
Agency Tracking Number: GM084603
Amount: $200,362.00
Phase: Phase I
Program: SBIR
Awards Year: 2008
Solicitation Year: 2008
Solicitation Topic Code: N/A
Solicitation Number: PHS2007-2
Small Business Information
DUNS: 804895600
HUBZone Owned: Y
Woman Owned: Y
Socially and Economically Disadvantaged: Y
Principal Investigator
 () -
Business Contact
Phone: (801) 703-5157
Research Institution
DESCRIPTION (provided by applicant): Many human diseases-if not all human diseases-and human health appear to be linked to our genetics. Major government and private research efforts are focused on investigating this linkage. Unfortunately, one of our bes t tools for this critical work-i.e., microarrays-holds us back, as most provide only generally qualitative results, limiting their usefulness. One key example is single nucleotide polymorphism (SNP) detection. Current SNP analysis is not quantitative becau se of imperfect molecular recognition (cross-hybridization) and pseudoequilibrium analyses performed with microarrays, limiting their use (e.g., to preliminary screening, as with the Affymetrix SNPChip). The microarray techniques attempt to compensate via excessive redundancy, leading to massive quantities of inaccurate/irreproducible data. The need to sort through these copious amounts of data extends analysis time, leads to improper conclusions, initiates scientific controversy, and may misdirect diagnost ic and pharmaceutical research. Fortunately, these outcomes can be improved upon-which is the primary goal of the multi-phase STTR Fast-Track project proposed here. One key task that requires next-generation tools for real-time, reliable, quantitative SNPs analysis-including new data-management/analysis capabilities and simple yet powerful chemistries-is heteroplasmy (semiquantitative mitochondrial DNA SNP assays). Heteroplasmy could fulfill a major unmet need for reliable/costefficient quantitative tests i nvolving cancer, diabetes, Alzheimer's disease, hypertension and a variety of neuromuscular, neurodegenerative, and metabolic diseases. Our goal is to develop, prototype, and commercialize real-time and quantitative heteroplasmy research tools based on tec hnology licensed from the U of Utah and developed by Sigma founders. Preliminary data using our proprietary competitive displacement analysis (CDA)-the key innovation-strongly indicates the potential for successful development and rapid commercialization under this Fast-Track project. Specifically, we propose to develop our new method of performing real-time SNP microarray analysis (via CDA) by monitoring non-linear binding kinetics of known competitors in the presence of unlabeled targets. Our Phase I Ai ms are to 1) Demonstrate relevant binding kinetics; 2) Prove/validate feasibility of using CDA for heteroplasmy-based SNP detection in a model system; and 3) Develop CDA-based analytical approaches for multi-component model systems, based on synthetic targ ets, competitors, and lower-affinity species (background). Meeting the key Phase I milestones will allow us to pursue Phase II Aims: 4) Characterize CDA for heteroplasmy analysis on A3243G mutation locus; 5) Scale up CDA to interrogate multiple mutations; and 6) Complete comparative validation of CDA versus reference methods. Phase II success will provide the data needed to attract Phase III industry and financial partners. This will facilitate rapid product introduction into a key niche in a multi-billio n-dollar research/diagnostics industry that benefits human health worldwide.

* Information listed above is at the time of submission. *

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