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 language | English |
|---|---|
| Pages (from-to) | 192-196 |
| Number of pages | 5 |
| Journal | Journal of Inorganic Biochemistry |
| Volume | 88 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - 15 Jan 2002 |
| Externally published | Yes |
Keywords
- Copper chaperone
- CopY
- Cu(I)
- Enterococcus hirae
- Metal-thiolate
- Metalloregulation
- Repressor
- Zn(II)