Mutations of human cytochrome P450 reductase differentially modulate heme oxygenase-1 activity and oligomerization

Christopher C. Marohnic, Warren J. Huber, J. Patrick Connick, James R. Reed, Karen McCammon, Satya P. Panda, Pavel Martásek, Wayne L. Backes, Bettie Sue S. Masters

Research output: Contribution to journalArticlepeer-review

17 Scopus citations


Genetic variations in POR, encoding NADPH-cytochrome P450 oxidoreductase (CYPOR), can diminish the function of numerous cytochromes P450, and also have the potential to block degradation of heme by heme oxygenase-1 (HO-1). Purified full-length human CYPOR, HO-1, and biliverdin reductase were reconstituted in lipid vesicles and assayed for NADPH-dependent conversion of heme to bilirubin. Naturally-occurring human CYPOR variants queried were: WT, A115V, Y181D, P228L, M263V, A287P, R457H, Y459H, and V492E. All CYPOR variants exhibited decreased bilirubin production relative to WT, with a lower apparent affinity of the CYPOR-HO-1 complex than WT. Addition of FMN or FAD partially restored the activities of Y181D, Y459H, and V492E. When mixed with WT CYPOR, only the Y181D CYPOR variant inhibited heme degradation by sequestering HO-1, whereas Y459H and V492E were unable to inhibit HO-1 activity suggesting that CYPOR variants might have differential binding affinities with redox partners. Titrating the CYPOR-HO-1 complex revealed that the optimal CYPOR:HO-1 ratio for activity was 1:2, lending evidence in support of productive HO-1 oligomerization, with higher ratios of CYPOR:HO-1 showing decreased activity. In conclusion, human POR mutations, shown to impact P450 activities, also result in varying degrees of diminished HO-1 activity, which may further complicate CYPOR deficiency.

Original languageEnglish (US)
Pages (from-to)42-50
Number of pages9
JournalArchives of Biochemistry and Biophysics
Issue number1
StatePublished - Sep 1 2011


  • HO-1
  • Heme
  • Oxygenase
  • P450
  • POR deficiency
  • Reductase

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology


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