Multiple Wavelength Anomalous Diffraction (MAD) Crystal Structure of Rusticyanin: a Highly Oxidizing Cupredoxin with Extreme Acid Stability

• Published in: Journal of molecular biology 1996-11, Vol.263 (5), p.730-751
• Main Authors: Walter, Richard L., Ealick, Steven E., Friedman, Alan M., Blake II, Robert C., Proctor, Peter, Shoham, Menachem
• Format: Article
• Language: English
• Subjects: acid stability; Azurin - analogs & derivatives; Azurin - chemistry; Azurin - metabolism; Bacterial Proteins - chemistry; Bacterial Proteins - metabolism; Binding Sites; Copper - metabolism; crystal structure; Crystallography, X-Ray; cupredoxins; Hydrogen-Ion Concentration; MAD phasing; Oxidation-Reduction; Protein Structure, Secondary; Protein Structure, Tertiary; rusticyanin; type-1 copper binding proteins; Tyrosine - chemistry
• ISSN: 0022-2836; 1089-8638
• DOI: 10.1006/jmbi.1996.0612

The X-ray crystal structure of the oxidized form of the extremely stable and highly oxidizing cupredoxin rusticyanin from Thiobacillus ferrooxidanshas been determined by the method of multiwavelength anomalous diffraction (MAD) and refined to 1.9 Å resolution. Like other cupredoxins, rusticyanin is a copper-containing metalloprotein, which is composed of a core β-sandwich fold. In rusticyanin the β-sandwich is composed of a six- and a seven-stranded β-sheet. Also like other cupredoxins, the copper ion is coordinated by a cluster of four conserved residues (His85, Cys138, His143, Met148) arranged in a distorted tetrahedron. Rusticyanin has a redox potential of 680 mV, roughly twice that of any other cupredoxin, and it is optimally active at pH values ≤2. By comparison with other cupredoxins, the three-dimensional structure of rusticyanin reveals several possible sources of the chemical differences, including more ordered secondary structure and more intersheet connectivity than other cupredoxins. The acid stability and redox potential of rusticyanin may also be enhanced over other cupredoxins by a more extensive internal hydrogen bonding network and by more extensive hydrophobic interactions surrounding the copper binding site. Finally, reduction in the number of charged residues surrounding the active site may also make a major contribution to acid stability. We propose that the resulting rigid copper binding site, which is constrained by the surrounding hydrophobic environment, structurally and electronically favours Cu(I). We propose that the two extreme chemical properties of rusticyanin are interrelated; the same unique structural features that enhance acid stability also lead to elevated redox potential.