SBIR/STTR Research Award

Development of an EFC Assay to Measure Growth Factor Receptor Dimer Formation for

Award identifier fe2fedb84bfd2d702fb434e3f159f58df52089533d9c29e6540ab045b2a49d43Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$113,104

Program and phase

SBIR · Phase I

Award year

2007

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
DISCOVERX CORPORATION
Proposal award date
Not reported
Contract end date
Not reported
UEI
HANEMEJA2KD7
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Cell surface receptors mediate the biological actions of growth factors. Most growth factor receptors are activated by ligand induced homo or heterodimerization. Because of their role in regulating cellular functions and the diseases caused by their disregulation, much interest exists in the pharmaceutical industry to develop drugs targeting growth factor receptors. In this grant, we propose to develop a novel technology that can be used to discover small molecule growth factor antagonists or agonists. The assay is based on our enzyme fragment complementation (EFC) technology that utilizes two genetically engineered fragments of E. coli a-gal. The larger fragment, Enzyme Acceptor (EA), contains a deletion near the amino terminus, while the smaller fragment, ProLabel, contains the amino-terminal sequence missing from EA. Alone, EA is inactive, but in vitro it can spontaneously recombine with ProLabel to form an active enzyme that can catalyze the formation of a luminescent product that can be detected photometrically. We have begun to adapt EFC to measure the interaction of different growth factor receptor subunits. The spontaneous, robust complementation of EA and ProLabel was transformed into a protein interaction detection system by mutating the ProLabel peptide to create a weakly complementing a-gal fragment termed ProLink. Because the system complements only weakly, when EA and ProLink are genetically fused to two proteins that interact, the interaction of the two proteins enhances the complementation resulting in increased a-gal activity. In this grant, we will provide proof of principle of the universality of the assay by developing EFC to measure activation of different subfamilies of growth factor receptors. These studies will provide the foundation of future phase II studies to optimize the assay format for HTS and initial drug discovery efforts against these different receptor subfamilies. This grant is focused on developing an assay that can measure the activation of any growth factor receptor in the Human Genome. This technology will allow for the discovery of novel small molecule drugs that regulate this important class of proteins and could provide for the generation of new drugs to treat a host of diseases including cancer and autoimmune disorders.

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Research funding history

14 SBIR/STTR records share this UEI (2000–2007). Reported award amounts total $2,880,871. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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