Cytochrome P450 Compound I: Capture, Characterization, and C-H Bond Activation Kinetics
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Abstract
Cytochrome P450 enzymes are responsible for the phase I metabolism of approximately 75% of known pharmaceuticals. P450s perform this and other important biological functions through the controlled activation of C-H bonds. Here, we report the spectroscopic and kinetic characterization of the long-sought principal intermediate involved in this process, P450 compound I (P450-I), which we prepared in approximately 75% yield by reacting ferric CYP119 with m-chloroperbenzoic acid. The Mössbauer spectrum of CYP119-I is similar to that of chloroperoxidase compound I, although its electron paramagnetic resonance spectrum reflects an increase in |J|/D, the ratio of the exchange coupling to the zero-field splitting.…
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Keywords
- Cytochrome P450
- Kinetics
- Chemistry
- Substrate (aquarium)
- Enzyme
- Oxidative phosphorylation
- Oxygen
- Stereochemistry
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