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Low Dose


EMSL Project ID
3205

Abstract

Although it is clear that understanding the protein complement of the cell is extremely important in understanding the function of the cell, the next stop in the further interpretion of pathways active with in the cell is to elucidate how the proteins are complexed. To this end, we are developing a high throughput method for isolating protein complexes from Shewanella oneidnesis using automated microfluidics. We will utilize the mass spectrometry capabilities with in the EMSL to characterize these compleses

Project Details

Project type
Exploratory Research
Start Date
2002-12-05
End Date
2005-10-06
Status
Closed

Team

Principal Investigator

Mary Lipton
Institution
Environmental Molecular Sciences Laboratory

Team Members

Cindy Bruckner-Lea
Institution
Pacific Northwest National Laboratory