Role for zinc(II) in the copper(I) regulated protein CopY

Paul A. Cobine, Christopher E. Jones, Charles T. Dameron

Research output: Contribution to journalArticlepeer-review

18 Citations (Scopus)

Abstract

Despite the importance of copper-thiolate clusters in the regulation of copper metabolism the formation chemistry of these clusters in proteins is not well understood. The number of Cu(I) ions that can be incorporated within a given molecule and their coordination number varies. CopY is a repressor protein from Enterococcus hirae which utilises a copper-thiolate cluster in the regulation of the copper homeostasis genes. Physical, biological assays of purified native reconstituted apoCopY suggest that the formation of a Zn(II)-protein prior to Cu(I) incorporation is necessary to achieve the native Cu(I)-S cluster. In this protein the Zn(II) is readily displaced by the Cu(I). CopY proteins with homologous metal binding motifs are being used to investigate cluster formation stabilisation.

Original languageEnglish
Pages (from-to)192-196
Number of pages5
JournalJournal of Inorganic Biochemistry
Volume88
Issue number2
DOIs
Publication statusPublished - 15 Jan 2002
Externally publishedYes

Keywords

  • Copper chaperone
  • CopY
  • Cu(I)
  • Enterococcus hirae
  • Metal-thiolate
  • Metalloregulation
  • Repressor
  • Zn(II)

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