期刊
JOURNAL OF BIOLOGICAL CHEMISTRY
卷 294, 期 6, 页码 1956-1966出版社
AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.RA118.005283
关键词
chaperone; copper transport; superoxide dismutase (SOD); protein complex; metallo-protein; metal ion-protein interaction; multifunctional enzyme; post-translational modification (PTM); oxidative stress; CCS1; dual chaperone; enzyme maturation; metallo-chaperone; copper-zinc superoxide dismutase (SOD1)
资金
- National Institutes of Health [R01 GM120252]
- Robert A. Welch Foundation [AT-1935-20170325]
- NIGMS, National Institutes of Health [R35GM128704]
- University of Texas at Dallas
Copper (Cu) is essential for the survival of aerobic organisms through its interaction with molecular oxygen (O-2). However, Cu's chemical properties also make it toxic, requiring specific cellular mechanisms for Cu uptake and handling, mediated by Cu chaperones. CCS1, the budding yeast (S. cerevisiae) Cu chaperone for Cu-zinc (Zn) superoxide dismutase (SOD1) activates by directly promoting both Cu delivery and disulfide formation in SOD1. The complete mechanistic details of this transaction along with recently proposed molecular chaperone-like functions for CCS1 remain undefined. Here, we present combined structural, spectroscopic, kinetic, and thermodynamic data that suggest a multifunctional chaperoning role(s) for CCS1 during SOD1 activation. We observed that CCS1 preferentially binds a completely immature form of SOD1 and that the SOD1CCS1 interaction promotes high-affinity Zn(II) binding in SOD1. Conserved aromatic residues within the CCS1 C-terminal domain are integral in these processes. Previously, we have shown that CCS1 delivers Cu(I) to an entry site at the SOD1CCS1 interface upon binding. We show here that Cu(I) is transferred from CCS1 to the entry site and then to the SOD1 active site by a thermodynamically driven affinity gradient. We also noted that efficient transfer from the entry site to the active site is entirely dependent upon the oxidation of the conserved intrasubunit disulfide bond in SOD1. Our results herein provide a solid foundation for proposing a complete molecular mechanism for CCS1 activity and reclassification as a first-of-its-kind dual chaperone.
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