SBIR/STTR Research Award
Imaging of Apoptosis
Award amount
$100,000Program and phase
SBIR · Phase IAward year
2001Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- MOLECULAR THERAPEUTICS, INC.
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
DESCRIPTION (provided by applicant): The long term goal of the proposed
project is to develop a transgenic rodent wherein activation of apoptosis can
be imaged non-invasively. Strict coordination of proliferation and apoptosis
is essential for normal physiology. An imbalance in these two opposing
processes results in various diseases including AIDS, neurodegenerative
disorders (Alzheimer's disease), myelodysplastic syndromes (Aplastic anemia,
thalassemia), ischemia/reperfusion injury, cancer and autoimmune disease among
others. Objective imaging of apoptosis will be a major advancement not only
in the screening and validation of novel therapeutic molecules for the above
diseases but also in the evaluation of therapeutic success or failure of
current and future therapeutic treatment paradigms. In phase I of this
proposal we will construct and test in a tissue culture a recombinant DNA
molecule that codes for an inactive luciferase protein which during apoptosis
becomes a functional luciferase enzyme thus enabling imaging of apoptosis.
The ability to image apoptosis non-invasively and dynamically over time will
be an invaluable resource to pharmaceutical companies for in vitro high
throughput screening of compounds with pro- and anti-apoptotic activity, but
also for target validation in vivo.
PROPOSED COMMERCIAL APPLICATION:
Apoptosis has been implicated in a wide variety of human diseases. The development of
drugs that specifically target enzymes involved in the apoptotic cascade is a vibrant and
dynamic research area. The ability to non-invasively image the effectiveness of these
drugs in vivo would be a breakthrough that would have significant market applications.
Technology keywords
Not reported