We have investigated Cu,Zn Superoxide Dismutase (Cu,Zn SOD) metal sites at
high pressure using X-ray absorption. XAS (X-ray Absorption Spectroscopy) g
ives information on local structure and it is particularly suited to metal
site investigation. To the best of our knowledge, this is the first time th
at protein conformational states have been investigated using the high pres
sure XAS technique. Cu, Zn SOD catalyses the dismutation of toxic ox)gen ra
dicals produced in cells; this reaction occurs at the copper metal site. St
ructural changes around the copper, induced by pressure, can be directly re
lated to protein substates. Their characterisation is thus important in the
understanding of protein activity.
The high-pressure device was a Paris-Edinburgh large volume cell.
Experiments were performed on lyophilised Cu, Zn SOD between 0 and 48 kbar
at the copper and zinc K-edges. The two metal local atomic environments hav
e a different behaviour as pressure increases: copper exhibits a more flexi
ble environment; on the contrary, zinc shows small structural modifications
. We have identified a state, formed between 3 and 8 kbar, which is stable
up to 48 kbar.