In this competitive renewal, the Proteomics Core is focused on the application and continued improvement ofcutting-edge proteomic technologies to study the process of hepatitis C virus (HCV) infection and its impacton liver function, AIDS, and the intravenous drug abuse population. To support these activities, the Centerhas teamed with the Biological Systems Analysis and Mass Spectrometry group headed by Dr. Richard D.Smith at Pacific Northwest National Laboratory (PNNL). This group brings to the effort unrivaled massspectrometry instrumentation and world-class proteomics expertise.
In Specific Aim 1, the Center will expandupon its use of unique, highly sensitive Fourier transform ion cyclotron mass spectrometry (FTICR-MS)instrumentation available at PNNL to investigate the clinical significance of HCV-associated proteinabundance changes using biopsy samples that provide limited protein yields. Applying proteomics to largersample sets from a broader spectrum of HCV-infected individuals (e.g., intravenous drug abuser and HIV-1co-infected patients) will provide a better understanding of the host response to HCV and HIV-1 infection andthe impact of drug abuse on basic HCV (HIV-1) infection biology.
In Specific Aim 2, we will leverageincreases in PNNL's throughput capabilities to extend our quantitative proteomic studies to multiple HCV andHIV-1 model systems (animal and cell culture). We will further leverage recent technological andmethodological advances that now permit in-depth proteome coverage of high dynamic range samples toanalyze additional sample types (human plasma samples complementary to liver biopsy tissues andHCV/HIV cell culture secreted proteins) not proposed in the original grant. The data generated from thesestudies will suport efforts to provide a detailed molecular portrait of the protein abundance changes thatoccur during the progression from HCV infection to end-stage liver disease and are likely to yield improveddiagnostic methods, markers of disease progression, and novel approaches to therapeutic intervention.
In Specific Aim 3, PNNL will provide the informatics resources needed to supply processed peptideidentification and quantification data to the NIDA Center for higher-order analyses and biologicalinterpretation. PNNL will also provide the raw MS data in various forms supporting release to the scientificcommunity for independent verification and comparison with other large-scale proteomic datasets.
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