TY - JOUR
T1 - Spectroscopic and computational study of a nonheme iron nitrosyl center in a biosynthetic model of nitric oxide reductase
AU - Chakraborty, Saumen
AU - Reed, Julian
AU - Ross, Matthew
AU - Nilges, Mark J.
AU - Petrik, Igor D.
AU - Ghosh, Soumya
AU - Hammes-Schiffer, Sharon
AU - Sage, J. Timothy
AU - Zhang, Yong
AU - Schulz, Charles E.
AU - Lu, Yi
PY - 2014/2/24
Y1 - 2014/2/24
N2 - A major barrier to understanding the mechanism of nitric oxide reductases (NORs) is the lack of a selective probe of NO binding to the nonheme Fe B center. By replacing the heme in a biosynthetic model of NORs, which structurally and functionally mimics NORs, with isostructural ZnPP, the electronic structure and functional properties of the FeB nitrosyl complex was probed. This approach allowed observation of the first S=3/2 nonheme {FeNO}7 complex in a protein-based model system of NOR. Detailed spectroscopic and computational studies show that the electronic state of the {FeNO}7 complex is best described as a high spin ferrous iron (S=2) antiferromagnetically coupled to an NO radical (S= 1/2) [Fe2+-NO .]. The radical nature of the FeB-bound NO would facilitate N-N bond formation by radical coupling with the heme-bound NO. This finding, therefore, supports the proposed trans mechanism of NO reduction by NORs. Ironed out: A nonheme iron nitrosyl complex has been prepared at a rationally designed FeB site within a myoglobin-based biosynthetic model of nitric oxide reductases (NORs) that contains a zinc protoporphyrin IX. The designed FeII-ZnPPFeBMb1 forms a nitrosyl complex [FeB2+-NO.] at the nonheme site. The radical nature of NO is implied to promote N-N bond formation by radical coupling, thus supporting the trans mechanism of NORs.
AB - A major barrier to understanding the mechanism of nitric oxide reductases (NORs) is the lack of a selective probe of NO binding to the nonheme Fe B center. By replacing the heme in a biosynthetic model of NORs, which structurally and functionally mimics NORs, with isostructural ZnPP, the electronic structure and functional properties of the FeB nitrosyl complex was probed. This approach allowed observation of the first S=3/2 nonheme {FeNO}7 complex in a protein-based model system of NOR. Detailed spectroscopic and computational studies show that the electronic state of the {FeNO}7 complex is best described as a high spin ferrous iron (S=2) antiferromagnetically coupled to an NO radical (S= 1/2) [Fe2+-NO .]. The radical nature of the FeB-bound NO would facilitate N-N bond formation by radical coupling with the heme-bound NO. This finding, therefore, supports the proposed trans mechanism of NO reduction by NORs. Ironed out: A nonheme iron nitrosyl complex has been prepared at a rationally designed FeB site within a myoglobin-based biosynthetic model of nitric oxide reductases (NORs) that contains a zinc protoporphyrin IX. The designed FeII-ZnPPFeBMb1 forms a nitrosyl complex [FeB2+-NO.] at the nonheme site. The radical nature of NO is implied to promote N-N bond formation by radical coupling, thus supporting the trans mechanism of NORs.
KW - EPR spectroscopy
KW - computational chemistry
KW - heme proteins
KW - iron
KW - reaction mechanisms
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U2 - 10.1002/anie.201308431
DO - 10.1002/anie.201308431
M3 - Article
C2 - 24481708
AN - SCOPUS:84894420721
SN - 1433-7851
VL - 53
SP - 2417
EP - 2421
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 9
ER -