The goal of this proposal is to develop a sensitive, high-throughput localized surface plasmon resonance assay for the detection of a wide range of biomarkers at levels reaching down to that of single molecules and with a highly scalable dynamic range. We have recently shown that plasmon resonant nanoparticles are highly sensitive to their proximity to nearby conductive substrates. They display large spectral shifts in resonance (or color) as well as changes in scattered light polarization upon nanometer-scale changes in distance from a nearby metal film. In addition, such nanoparticles are also effective labels for biomolecules because of their ease of functionalization and detection. Proposed here is a scheme whereby plasmon resonant nanoparticles and metal surfaces are functionalized with capture molecules designed to recognize specific biomarkers varying in size from small molecules/DNA targets to proteins. Upon exposure to clinical samples, the functionalized nanoparticles bind target analytes and are then directed to specific areas on conductive substrates defined by surface patterns of complimentary capture molecules. The completely novel innovation proposed here is that targets bound to nanoparticles will be detected and discriminated from nonspecific adsorption of nanoparticles without targets by searching in a digital image for a predetermined nanoparticle color and/or scattering polarization that is specific to the physical size (and hence, spacing between nanoparticle and film) determined by bound target.
Specific aims of this proposal are as follows: 1. Optimization of the sensor response. 2. Design of """"""""receptor"""""""" functionalized NPs and fabrication of sensor chips. 3. Detect clinical analytes. Public Health Relevance: As our knowledge of disease expands the need to reliably detect biomolecules of various sizes and concentrations becomes more important. The goal of this work is to develop a novel detection platform that is scalable from the single molecule level to the multiplexed assay level where signal is easily disguishable from background noise, thus increasing the accuracy, sensitivy, and applicability of clinical biomarker assays.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
1F32EB009299-01A1
Application #
7676425
Study Section
Special Emphasis Panel (ZRG1-F14-G (20))
Program Officer
Erim, Zeynep
Project Start
2009-08-01
Project End
2011-07-31
Budget Start
2009-08-01
Budget End
2010-07-31
Support Year
1
Fiscal Year
2009
Total Cost
$50,054
Indirect Cost
Name
Duke University
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
044387793
City
Durham
State
NC
Country
United States
Zip Code
27705
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Mock, Jack J; Hill, Ryan T; Tsai, Yu-Ju et al. (2012) Probing dynamically tunable localized surface plasmon resonances of film-coupled nanoparticles by evanescent wave excitation. Nano Lett 12:1757-64
Ciracì, C; Hill, R T; Mock, J J et al. (2012) Probing the ultimate limits of plasmonic enhancement. Science 337:1072-4
Hill, Ryan T; Mock, Jack J; Hucknall, Angus et al. (2012) Plasmon ruler with angstrom length resolution. ACS Nano 6:9237-46
Hill, Ryan T; Mock, Jack J; Urzhumov, Yaroslav et al. (2010) Leveraging nanoscale plasmonic modes to achieve reproducible enhancement of light. Nano Lett 10:4150-4
Jenness, Nathan J; Hill, Ryan T; Hucknall, Angus et al. (2010) A versatile diffractive maskless lithography for single-shot and serial microfabrication. Opt Express 18:11754-62