J. Biol. Chem.-2018-Freeman-5210-9.pdf (1.85 MB)
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Solution structure of the cytochrome P450 reductase–cytochrome c complex determined by neutron scattering

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journal contribution
posted on 30.04.2018, 15:55 by Samuel L. Freeman, Anne Martel, Juliette M. Devos, Jaswir Basran, Emma L. Raven, Gordon C. K. Roberts
Electron transfer in all living organisms critically relies on formation of complexes between the proteins involved. The function of these complexes requires specificity of the interaction to allow for selective electron transfer but also a fast turnover of the complex, and they are therefore often transient in nature, making them challenging to study. Here, using small-angle neutron scattering with contrast matching with deuterated protein, we report the solution structure of the electron transfer complex between cytochrome P450 reductase (CPR) and its electron transfer partner cytochrome c This is the first reported solution structure of a complex between CPR and an electron transfer partner. The structure shows that the interprotein interface includes residues from both the FMN- and FAD-binding domains of CPR. In addition, the FMN is close to the heme of cytochrome c but distant from the FAD, indicating that domain movement is required between the electron transfer steps in the catalytic cycle of CPR. In summary, our results reveal key details of the CPR catalytic mechanism, including interactions of two domains of the reductase with cytochrome c and motions of these domains relative to one another. These findings shed light on interprotein electron transfer in this system and illustrate a powerful approach for studying solution structures of protein-protein complexes.

History

Citation

Journal of Biological Chemistry, 2018, 293 (14), pp. 5210-5219

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/Biological Sciences/Old Departments Pre 01 Aug 2015/Department of Biochemistry (Pre 01 Aug 2015)

Version

VoR (Version of Record)

Published in

Journal of Biological Chemistry

Publisher

American Society for Biochemistry and Molecular Biology

issn

0021-9258

eissn

1083-351X

Copyright date

2018

Available date

30/04/2018

Publisher version

http://www.jbc.org/content/293/14/5210

Language

en