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Jeremy Driskell - Tripp Lab, UGA

Viral Immunology: Tripp Laboratory

Jeremy Driskell, PhD

Jeremy looking at his newest nano substrate

jdriskel@uga.edu

Animal Health Research Center, Room 113

Office: (706) 542-2205


Research Interests

Development of diagnostic methods for rapid and sensitive identification of viruses is essential for the advancement of therapeutic and preventive intervention strategies necessary to protect public health. Current diagnostic methods, including virus isolation, PCR, antigen detection and serology, are time-consuming, cumbersome, or lack the required sensitivity. Thus, there is a critical need to develop novel strategies to overcome the limitations of these traditional methods.
My research focuses on the integration of nanotechnology, spectroscopy, chemistry, and multivariate statistical analysis for the direct detection and classification of intact whole viruses. This method relies on surface-enhanced Raman spectroscopy (SERS) for viral fingerprinting. The strength of a SERS-based biosensor is its abilities to detect extremely low levels of material and to provide virus-specific structural information for identification. Historically, SERS has been limited by the lack of a technology to reproducibly fabricate nanostructured surfaces required for SERS. Recently, oblique angle deposition (OAD) has been developed for the fabrication of nanorod arrays which provides the reproducibility required for SERS-based viral fingerprinting.
OAD-fabricated substrates have been employed to collect SERS spectral libraries for several viruses, including respiratory syncytial virus (RSV), HIV, measles virus, influenza, and rotavirus.  Chemometric analysis of the intrinsic SERS spectra collected from these assays facilitates classification of the virus samples, and the results demonstrate that this method has the specificity to differentiate between different strains of a single virus.

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Publications

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Book Chapters

  • Kenseth JR, Kwarta KM, Driskell JD, Porter MD, Neill JD, Ridpath JF. Strategies in the use of atomic force microscopy as a multiplexed readout tool of chip-scale protein motifs. Combinatorial Materials Science. S. Mallapragada and B. Narasimhan, Eds.; Wiley, 2007.
  • Park HY, Driskell JD, Kwarta KM, Lipert RJ, Porter MD, Schoen C, Neill JD, Ridpath JF. Ultrasensitive immunoassays based on surface-enhanced Raman scattering by immunogold labels” Surface-Enhanced Raman Scattering – Physics and Applications. K. Kneipp, H. Kneipp, and M. Moskovits, Eds.; Springer, 2006.
  • Driskell JD, Shanmukh S, Liu Y, Chaney S, Hennigan S, Jones L, Krause D, Tripp RA, Zhao YP, Dluhy RA. Novel nanoarray SERS substrates used for high sensitivity virus biosensing and classification. Nanoscience and Nanotechnology for Chembio Defense. Ramanathan, Ed.; ACS, 2007 in press.

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This page last updated March 10, 2010 .