Protein kinases are chemically tractable drug targets, yet less than 5% of the human kinome has been thoroughly explored with selective small molecule inhibitors to demonstrate their therapeutic utility. Pharmaceutical companies are interested in evaluation of the therapeutic potential of targeting kinases to define new opportunities to address unmet medical needs. Lucidicor, Inc. has identified and extensively engineered an unusual marine-derived protein, termed PhosFluor", which varies its fluorescence upon phosphorylation. We have extensively engineered native PhosFluor" using Protein Kinase A as a prototype, and are developing this into a cell-based fluorescence assay that provides real-time in vivo visualization of protein phosphorylation. This platform can be applied to virtually any of the 518 protein kinases of the human kinome. The objective of this application is to optimize our novel cell-based platform to respond to protein kinase inhibitors. The working hypothesis is that PhosFluor" can easily be engineered to fluoresce in response to other protein kinases, and can therefore be used monitor the action of compounds that have been developed to modulate protein kinases. Our experimental approach will be to create additional PhosFluor" derivatives by converting engineered phosphorylation sites into substrate sequences for a tyrosine kinase (Fyn kinase) and a cyclin-dependent protein kinase (cdk5). The rationale for the proposed research is that many well-characterized compounds have already been developed for these kinases, and that the successful testing of these biosensors will enable us to determine the effectiveness of our screening method. The proposed research is significant, because it is offers a novel cellular screening platform for new drugs to target kinases and phosphatases, which may result in innovative treatments for disorders such as cancer, inflammation, pain and neuropsychiatric disorders. Finally, this new technology will be convertible to a wide array of protein kinases, greatly expanding the number of drug targets that may potentially be screened.
Public Health Relevance Statement: Public Health Relevance: The proposed research is relevant to public health because developing methods to study and screen protein kinases is ultimately expected to facilitate the search for compounds that may be efficacious for various diseases, including inflammation, cancer, neurological disorders and metabolic conditions. Thus, the proposed research is relevant to mission of the NIH to eliminate suffering and death due to disease.
Project Terms: Academia; Address; base; Binding (Molecular Function); Biological; Biological Assay; Biological Sciences; Biology; Biosensor; Cell Line; Cells; Cessation of life; Cloning; Communities; Cyclic AMP-Dependent Protein Kinases; Cyclin-Dependent Kinases; Development; Disease; Dissociation; drug discovery; Drug Industry; Drug Targeting; Ecosystem; Effectiveness; Engineering; Exhibits; Expeditions; Fluorescence; Fostering; Human; Human Cell Line; Imagery; In Vitro; in vivo; Inflammation; inhibitor/antagonist; Inhibitory Concentration 50; innovation; interest; kinase inhibitor; Knowledge; Legal patent; Letters; Life; Malignant Neoplasms; Mammalian Cell; Marines; Medical; Metabolic; Methods; Mission; Molecular; Monitor; Nature; nervous system disorder; neuropsychiatry; new technology; novel; novel therapeutics; Outcome; Pain; Pharmaceutical Preparations; Pharmacologic Substance; Phase; Phosphoric Monoester Hydrolases; Phosphorylation; Phosphorylation Site; Phosphotransferases; Physiological Processes; Process; Protein Kinase; protein kinase inhibitor; Protein Kinase Inhibitors; protein kinase modulator; Proteins; Proto-Oncogene Proteins c-fyn; prototype; public health medicine (field); public health relevance; Research; response; Scientist; screening; Services; Small Business Innovation Research Grant; small molecule; Technology; Testing; Therapeutic; therapeutic evaluation; Time; tool; Translational Research; translational study; United States National Institutes of Health; Work
