Alteration of the oxygen-dependent reactivity of de novo Due Ferri proteins

• Published in: Nature chemistry 2012-11, Vol.4 (11), p.900-906
• Main Authors: Reig, Amanda J., Pires, Marcos M., Snyder, Rae Ana, Wu, Yibing, Jo, Hyunil, Kulp, Daniel W., Butch, Susan E., Calhoun, Jennifer R., Szyperski, Thomas, Solomon, Edward I., DeGrado, William F.
• Format: Article
• Language: English
• Subjects: 639/638/263; 639/638/45/535; 639/638/92/469; Amino Acid Sequence; Amino acids; Analytical Chemistry; Biochemistry; Ceruloplasmin - metabolism; Chemistry; Chemistry/Food Science; Drug Design; Electrons; Enzymes; Hydroquinones - chemistry; Hydroquinones - metabolism; Hydroxylation; Inorganic Chemistry; Iron; Iron-Binding Proteins - chemistry; Iron-Binding Proteins - metabolism; Kinetics; Ligands; Models, Molecular; Molecular Sequence Data; Mutation; Organic Chemistry; Oxidation; Oxygen - metabolism; Physical Chemistry; Protein Folding; Protein Stability; Protein Structure, Secondary; Proteins
• ISSN: 1755-4330; 1755-4349
• DOI: 10.1038/nchem.1454

De novo proteins provide a unique opportunity to investigate the structure–function relationships of metalloproteins in a minimal, well-defined and controlled scaffold. Here, we describe the rational programming of function in a de novo designed di-iron carboxylate protein from the Due Ferri family. Originally created to catalyse the O 2 -dependent, two-electron oxidation of hydroquinones, the protein was reprogrammed to catalyse the selective N -hydroxylation of arylamines by remodelling the substrate access cavity and introducing a critical third His ligand to the metal-binding cavity. Additional second- and third-shell modifications were required to stabilize the His ligand in the core of the protein. These structural changes resulted in at least a 10 6 -fold increase in the relative rate between the arylamine N -hydroxylation and hydroquinone oxidation reactions. This result highlights the potential for using de novo proteins as scaffolds for future investigations of the geometric and electronic factors that influence the catalytic tuning of di-iron active sites. Representing the first successful rational reprogramming of function in a de novo protein, the reactivity of a designed di-iron carboxylate protein from the Due Ferri family was altered from hydroquinone oxidation to arylamine N -hydroxylation through the introduction of a critical third histidine ligand in the active site.