Metal ions such as Fe and Cu play an essential role in many cellular processes including energy production, biosynthesis and antioxidation. The key to their usefulness as enzyme cofactors lies in their ability to participate in electron transfer and to catalyze redox reactions. Yet this very chemistry imposes a stringent requirement to regulate the speciation, concentration and transport of cellular metal ions, since the free ions are themselves highly cytotoxic via Fenton mediated chemistry. Heme copper oxidases (HCOs) are classic examples of essential metalloproteins, and are utilized as the terminal electron acceptors in many prokaryotic and eukaryotic electron transfer chains. HCOs have evolved complex processes to assemble and metalate the multisubunit structures that are required for enzyme activity. In particular, the copper-binding Sco chaperone is required for the correct assembly and metalation of the mixed-valence dinuclear CuA center, which resides in subunit 2, and accepts electrons into the oxidase from cytochrome c. The chemistry at the heart of these cellular processes involves the exchange of CuI or CuII from chaperone to enzyme or transporter via molecular mechanisms which are only poorly understood. In this proposal we build on advanced spectroscopic methodologies developed in our laboratory to unravel the detailed mechanisms of metal transport and exchange. These experiments are underpinned by our expertise in X-ray absorption spectroscopy which is the only spectroscopic technique capable of directly observing the CuI state as it is transferred along the homeostatic pathways. Specifically we propose to apply the technique of Se labeling coupled to XAS detection to investigate the metallation of the CuA center by its putative chaperone Sco and by the periplasmic copper-binding protein PCuAC or its homologues. Spectroscopic and kinetic studies of metal transfer will be correlated with function across a number of different prokaryotic and eukaryotic systems, using relationships between mutagenesis and phenotype to elucidate the structural determinants of the transfer mechanism. These studies will lead to a better understanding of the molecular basis of copper trafficking and will aid in combating diseases of aberrant copper homeostasis.

Public Health Relevance

Cells have evolved complex molecular machinery to maintain metal ion concentrations within a narrow range since free metal ions are highly cytotoxic. Because of this, genetic defects in the regulation of cellular copper levels lead to diseases such as Menkes and Wilson diseases, while neurodegenerative disorders including ALS, Alzheimer's, and Parkinson's disease have been associated with mutations in copper enzymes (SOD), or abnormal copper levels. This proposal aims to develop new methods based on advanced spectroscopy to gain a more detailed understanding of the molecular mechanisms involved in metal ion trafficking, and thereby to contribute to the science that will eventually provide cures for diseases of aberrant metal ion homeostasis.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM054803-14
Application #
8461129
Study Section
Macromolecular Structure and Function A Study Section (MSFA)
Program Officer
Anderson, Vernon
Project Start
1997-05-01
Project End
2016-02-29
Budget Start
2013-03-01
Budget End
2014-02-28
Support Year
14
Fiscal Year
2013
Total Cost
$252,543
Indirect Cost
$83,668
Name
Oregon Health and Science University
Department
Engineering (All Types)
Type
Schools of Medicine
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
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