NR AMAR
AU Viles,J.H.; Cohen,F.E.; Prusiner,S.B.; Goodin,D.B.; Wright,P.E.; Dyson,H.J.
TI Copper binding to the prion protein: structural implications of four identical cooperative binding sites.
QU Proceedings of the National Academy of Sciences of the United States of America 1999 Mar 2; 96(5): 2042-7
PT journal article
AB Evidence is growing to support a functional role for the prion protein (PrP) in copper metabolism. Copper ions appear to bind to the protein in a highly conserved octapeptide repeat region (sequence PHGGGWGQ) near the N terminus. To delineate the site and mode of binding of Cu(II) to the PrP, the copper-binding properties of peptides of varying lengths corresponding to 2-, 3-, and 4-octarepeat sequences have been probed by using various spectroscopic techniques. A two-octarepeat peptide binds a single Cu(II) ion with Kd approximately 6 microM whereas a four-octarepeat peptide cooperatively binds four Cu(II) ions. Circular dichroism spectra indicate a distinctive structuring of the octarepeat region on Cu(II) binding. Visible absorption, visible circular dichroism, and electron spin resonance spectra suggest that the coordination sphere of the copper is identical for 2, 3, or 4 octarepeats, consisting of a square-planar geometry with three nitrogen ligands and one oxygen ligand. Consistent with the pH dependence of Cu(II) binding, proton NMR spectroscopy indicates that the histidine residues in each octarepeat are coordinated to the Cu(II) ion. Our working model for the structure of the complex shows the histidine residues in successive octarepeats bridged between two copper ions, with both the Nepsilon2 and Ndelta1 imidazole nitrogen of each histidine residue coordinated and the remaining coordination sites occupied by a backbone amide nitrogen and a water molecule. This arrangement accounts for the cooperative nature of complex formation and for the apparent evolutionary requirement for four octarepeats in the PrP.
MH Amino Acid Sequence; Binding Sites; Circular Dichroism; Copper/*metabolism; Electron Spin Resonance Spectroscopy; Kinetics; Models, Molecular; Molecular Sequence Data; Peptide Fragments/chemistry; Prions/*chemistry/*metabolism; *Protein Conformation; Repetitive Sequences, Amino Acid; Support, U.S. Gov't, P.H.S.
AD Scripps Research Institute, La Jolla, CA 90237, USA
SP englisch
PO USA