Using macromolecular neutron crystallography to study hydrogen atoms in the catalytic mechanism of the FADH cofactor in cholesterol oxidase

The protein microenvironment surrounding the flavin cofactor in flavoenzymes is key to the efficiency and diversity of reactions catalysed by this class of enzymes. X-ray diffraction structures of oxidoreductase flavoenzymes have revealed recurrent features which facilitate catalysis, such as a hydrogen bond between a main chain nitrogen atom and the flavin redox center (N5). A neutron diffraction study of cholesterol oxidase has revealed an unusual elongated main chain nitrogen to hydrogen bond distance positioning the hydrogen atom towards the flavin N5 reactive center. Investigation of the structural features which could cause such an unusual occurrence revealed a positively charged lysine side chain, conserved in other flavin mediated oxidoreductases, in a second shell away from the FAD cofactor acting to polarize the peptide bond through interaction with the carbonyl oxygen atom. Double-hybrid density functional theory calculations confirm that this electrostatic arrangement affects the N-H bond length in the region of the flavin reactive center. We propose a novel second-order partial-charge interaction network which enables the correct orientation of the hydride receiving orbital of N5. The implications of these observations for flavin mediated redox chemistry are discussed.

Keywords

Proteins, Isoalloxazines, Enzymes, X-ray diffraction, Oxidoreductases, Neutron diffraction, Cholesterol

Citation

Golden, E., Yu, L.-J., Meilleur, F., Blakeley, M., Duff, A., Karton, A., & Vrielink, A. (2017). Using macromolecular neutron crystallography to study hydrogen atoms in the catalytic mechanism of the FADH cofactor in cholesterol oxidase. Paper presented at ICNS 2017 (International Conference on Neutron Scattering), Daejeon, South Korea, 9 to 13 July 2017. Retrieved from: http://www.icns2017.org/program.php

URI

http://www.icns2017.org/program.php
https://apo.ansto.gov.au/dspace/handle/10238/11377

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