Rapid detection of infectious agents has become more relevant with concerns associated with detection of bioterrorist agents. Current technology for detection and quantification of clinically relevant molecules is based on monoclonal and polyclonal antibodies used for immunoassay or detection of nucleic acids using RT-PCR systems. These assays are relatively slow taking at least 3 hours to complete. A novel, rapid, immunoproteomics assay based on high affinity specific antibodies coupled with a mass spectral read out is proposed. In a series of preliminary studies we have demonstrated the ability to use a single antibody-coated antigen capture and transfer reagent (ACTR) to detect model antigens, with good sensitivity, using surface enhanced laser desorption ionization time-of-flight mass spectrometry (SELDI-TOF). This immunoproteomic assay can be complete in < 1 hour and follows a sequential process in which antibody is immobilized in step 1, antigen is captured in step 2 and bound antigen is analyzed by mass spectrometry in step 3. Immunoproteomic assays may potentially be faster and as sensitive as the current antibody assays and could provide evidence for bacterial or viral antigens or specific antibodies to these products in samples for an infected animal. This RO3 proposal is designed to optimize this platform technology. In the initial proof-of-concept studies, we will develop and evaluate immunoproteomic assays to measure INF gamma (Th1 cytokine) and specific anti-viral antibodies in the serum of ectromelia infected mice. Ectromelia is a surrogate of variola virus, a CDC Category A bioterrorist agent and thus, the successful immunoproteomic approach may be relevant for detection of bioterrorist agents.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Small Research Grants (R03)
Project #
5R03AI053718-02
Application #
6792044
Study Section
Experimental Virology Study Section (EVR)
Program Officer
Gondre-Lewis, Timothy A
Project Start
2003-08-15
Project End
2006-07-31
Budget Start
2004-08-01
Budget End
2006-07-31
Support Year
2
Fiscal Year
2004
Total Cost
$58,256
Indirect Cost
Name
Juniata College
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
072845035
City
Huntingdon
State
PA
Country
United States
Zip Code
16652
Hess, Jennifer L; Porsch, Eric A; Shertz, Cecelia A et al. (2007) Immunoglobulin cleavage by the streptococcal cysteine protease IdeS can be detected using protein G capture and mass spectrometry. J Microbiol Methods 70:284-91
Blazer, Levi L; Boyle, Michael D P (2007) Use of protein chip mass spectrometry to monitor biotinylation reactions. Appl Microbiol Biotechnol 74:717-22
Coyle, Emily M; Blazer, Levi L; White, Abby A et al. (2006) Practical applications of high-affinity, albumin-binding proteins from a group G streptococcal isolate. Appl Microbiol Biotechnol 71:39-45
Boyle, Michael D P; Hess, Jennifer L; Nuara, Anthony A et al. (2006) Application of immunoproteomics to rapid cytokine detection. Methods 38:342-50
Hess, Jennifer L; Blazer, Levi; Romer, Terence et al. (2005) Immunoproteomics. J Chromatogr B Analyt Technol Biomed Life Sci 815:65-75