The broad goal of the research in the area is to develop a complete mechanistic description of the proteins, regulatory processes and mechanisms involved in the intracellular routing of copper. Exciting developments over the past decade have lead to an increase in the understanding of copper homeostasis, its essentiality, toxicity and pivotal role in metabolism. The unique redox properties of copper make it an essential cofactor for a wide range of critical enzymes. Although these enzymes are readily identified (cytochrome c oxidase, superoxide dismutase, dopamine phydroxylase etc.) it is still not understood how copper is transported through the body, across membranes, incorporated into enzymes, recycled and excess excreted. Still less is understood about the mechanisms of these processes in normal and diseased states. It is clear that sever dysfunctions result from defects in copper metabolism, encountered in some human genetic diseases likeJvlenkes and Wilsons. Utilizing the features of the simple, highly characterized Enteroccus hirae bacterial system, that contributed previously to the understanding of copper metabolism, key mechanistic and regulatory questions will be investigated.
The specific aims are: 1) characterize the putative transfer of copper from an import protein to a intracellular transport protein 2) evaluate the role of the metal ligands in a transport protein to attract and donate copper ions 3) define, at a molecular level, the metal sensing mechanism of a regulatory molecule. Accomplishment of these goals will further advance the understanding of the mechanisms and the - regulation of the copper import and cellular distribution processes.
| Collins, Tyler C; Dameron, Charles T (2012) Dissecting the dimerization motif of Enterococcus hirae's Zn(II)CopY. J Biol Inorg Chem 17:1063-70 |
| Pazehoski, Kristina O; Cobine, Paul A; Winzor, Donald J et al. (2011) Evidence for involvement of the C-terminal domain in the dimerization of the CopY repressor protein from Enterococcus hirae. Biochem Biophys Res Commun 406:183-7 |
| Pazehoski, Kristina O; Collins, Tyler C; Boyle, Robert J et al. (2008) Stalking metal-linked dimers. J Inorg Biochem 102:522-31 |
