Directory: Faculty

Jennifer S. Shumaker-Parry

ANALYTICAL CHEMISTRY

Assistant Professor

B.S. University of South Dakota, 1995
Ph.D. University of Washington, 2002
NSF Mathematical and Physical Sciences Distinguished International Postdoctoral Research Fellow (MPS-DRF), Max Planck Institute for Polymer Research, Mainz, Germany, 2003-2004

Phone: (801) 585-1434

Office: 2504 HEB-S

Email: shumaker-parry@chem.utah.edu

Interfacial & Bioanalytical Chemistry (IBAC)

Publications

Research Interests

Molecular recognition plays a central role in biology by controlling cellular processes such as enzymatic catalysis, transport, regulation and communication. We are developing and applying high-throughput sensing methods based on surface plasmon resonance (SPR) to study molecular recognition between biomolecules. SPR-based sensing provides real-time, quantitative analysis of biomolecule interactions without the need for labels. Detailed information about the strength and specificity of biomolecule interactions impacts medical research, diagnostics, drug discovery and fundamental molecular biology studies. This multi-disciplinary research requires methods and tools from analytical chemistry, surface chemistry, biochemistry, materials science, nano\microfabrication, and microscopy.

Localized Surface Plasmon Resonance (LSPR) Sensing with Nanoparticles. We are developing novel nanoparticles as specific and sensitive nano-sized sensors. Metallic nanoparticle sensors are based on measuring changes in the LSPR when target molecules bind to surface-immobilized receptors. We are tailoring nanoparticle optical properties and developing methods for multiplexing, label-free analysis.

Cartoon of (a) a single nanoparticle sensor and (b) spectra (i.e., light scattering or extinction) for monitoring binding events.

Cartoon of (a) a single nanoparticle sensor and (b) spectra (i.e., light scattering or extinction) for monitoring binding events.

Irregularly-Shaped Nanoparticles. One approach for tailoring nanoparticle properties is to control the physical structure. Noble metal nanoparticles exhibit plasmon resonances that depend on their size, shape and local environment. We are fabricating irregularly-shaped (i.e., non-spherical) nanostructures that exhibit unique plasmon resonances and localized field enhancements.

We are characterizing the nanoparticles using scanning electron microscopy (SEM), atomic force microscopy (AFM), UV-visible spectroscopy and dark field microscopy. Irregularly-shaped nanoparticles have potential application in bioanalytical chemistry, including surface-enhanced spectroscopies (e.g., Surface-Enhanced Raman Spectroscopy (SERS), Surface-Enhanced Infrared Spectroscopy, and Plasmon-Enhanced Fluorescence Spectroscopy).

SPR Microscopy for Array-Based Analysis of Biomolecule Interactions. SPR microscopy is emerging as an important technique for array-based molecular recognition studies. SPR microscopy provides a label- free method for high-throughput, quantitative, real-time kinetic studies of biomolecule interactions (e.g., protein-DNA, protein-protein, protein-vesicle). We are using SPR microscopy for array-based analysis and optimizing sensor surface chemistry and immobilization of binding partners (e.g., proteins or DNAs) for array fabrication.

topSelected Publications