Phase II year
2015
(last award dollars: 2016)
Phase II Amount
$1,020,836
Real-time label-free technologies such as surface plasmon resonance biosensors provide high-resolution information about the kinetics, affinity, stoichiometry, activity, and specificity, of two (or more) binding partners. While the application f biosensors is well established, current instrumentation has limited sampling throughput. Screens of even a fairly small chemical library (e.g., 3000-5000 compounds) require days to weeks to complete using traditional label-free instruments. Because of the quality of the data generated by SPR, drug discovery scientists are clamoring to use enhanced biosensors as a screening tool for small molecule applications; however, lack of throughput hinders their ability to move in this direction. We propose to develop a biosensor platform that has increased throughput yet maintains the data quality and ease of use to which researchers are accustomed. We will couple our novel Continuous Flow Microspotter (CFM) with an enhanced-sensitivity SPR biosensor from BiOptix to enable label-free screening and kinetic analsyis of small molecules and biologics. In high-throughput screening mode our 96 channel integrated CFM/E-biosensor platform will be capable of collecting data for >30,000 samples in less than 24 hours - a sampling rate 24x faster than fastest small-molecule capable label-free biosensor, the Biacore 4000.
Public Health Relevance Statement: Public Health Relevance: Label-free real-time biosensors enable the measurement of the kinetics of biomolecule binding. Getting this information earlier in the drug discovery process reduces false positives, identifies candidates that may have been missed, improves subject matter for patent filings, and increases the probability of the selected candidate's eventual success. Traditional label-free biosensors have limited sample throughput, which has restricted their use to secondary roles. By combining our highly parallel microfluidic sample delivery technology with a small-molecule sensitive biosensor, we will enable the high-throughput label-free analysis of small molecules and biologics, which offers significant potential for increasing the efficiency of early stage drug discovery.
NIH Spending Category: Bioengineering; Biotechnology; Networking and Information Technology R&D
Project Terms: Affinity; Antibodies; Antigens; Automation; Binding (Molecular Function); Biosensing Techniques; Biosensor; Chemistry; Computer software; computerized data processing; cost; Coupling; Data; Data Analyses; Data Collection; Data Quality; Detection; detector; Devices; drug discovery; Grant; Healthcare; high throughput screening; Hour; Image; Imaging technology; improved; industry partner; instrument; instrumentation; Interferometry; Investments; Kinetics; Label; Legal patent; Libraries; Light; Location; Marketing; Measurement; Membrane; Microfluidics; Molecular Weight; Monitor; novel; Pharmaceutical Preparations; Pharmacologic Substance; Phase; Phosphotransferases; Preparation; pressure; Probability; Process; protein protein interaction; Protocols documentation; public health relevance; Race; Research; research and development; Research Personnel; Resolution; Risk; Role; Sampling; Sampling Studies; Scientist; screening; Secondary to; sensor; Small Business Technology Transfer Research; small molecule; small molecule libraries; Specificity; Spottings; Staging; stoichiometry; success; Surface; Surface Plasmon Resonance; System; Technology; Testing; Time; tool; Work
