PNNL lands $10.3 million NIH biodefense contract to unlock proteomes of salmonella and pox
5-year project will explore how our cells interact with infectious-agents and point the way to new, fast-acting drugs
September 10, 2004
RICHLAND, Wash. –
Pacific Northwest National Laboratory has received a $10.3 million biodefense contract from the National Institute of Allergies and Infectious Diseases (NIAID) to identify the proteins that regulate the bacteria that cause salmonella poisoning and typhoid fever, and the monkey pox virus.
The five-year award is the Department of Energy lab's third $10 million National Institutes of Health grant or contract in the past year and the second for Richard D. Smith, principal investigator and a Battelle Fellow at PNNL.
Besides monkey pox, which serves as a close viral analog to deadly smallpox, two species from the genus Salmonella will be examined: typhimurium (which causes food poisoning) and typhi (typhoid fever). These pathogens, which spread quickly and are not easily combated with conventional drugs, could lead to major epidemics if enlisted by terrorists. NIAID is banking that determining which microbial proteins interact with which human host cells will point drug designers toward quick and effective treatments during an outbreak.
To conduct the analysis of these microbial proteins, scientists at PNNL will use proteomics instruments and approaches unavailable elsewhere that simultaneously combine the high-resolution separation of proteins with their identification, on a suite of powerful mass spectrometers developed at the W.R. Wiley Environmental Molecular Science Laboratory on the PNNL campus.
Collaborators at Oregon Health & Science University in Portland will prepare the infectious agents for the proteomics at PNNL and will assist in analyzing the data generated there. The OHSU group has been able to knock out key genes that regulate the degree of pathogenic activity in the microbes. This capability will allow researchers to test proteins identified at PNNL as candidates to be targeted by drugs.
Tags: Energy, Fundamental Science, Proteomics