Polyethylene glycol promotes autoxidation of cytochrome c

Biochim Biophys Acta Gen Subj. 2018 Jun;1862(6):1339-1349. doi: 10.1016/j.bbagen.2018.03.010. Epub 2018 Mar 11.

Abstract

Cytochrome c (Cyt c) was rapidly oxidized by molecular oxygen in the presence, but not absence of PEG. The redox potential of heme c was determined by the potentiometric titration to be +236 ± 3 mV in the absence of PEG, which was negatively shifted to +200 ± 4 mV in the presence of PEG. The underlying the rapid oxidation was explored by examining the structural changes in Cyt c in the presence of PEG using UV-visible absorption, circular dichroism, resonance Raman, and fluorescence spectroscopies. These spectroscopic analyses suggested that heme oxidation was induced by a modest tertiary structural change accompanied by a slight shift in the heme position (<1.0 Å) rather than by partial denaturation, as is observed in the presence of cardiolipin. The near-infrared spectra showed that PEG induced dehydration from Cyt c, which triggered heme displacement. The primary dehydration site was estimated to be around surface-exposed hydrophobic residues near the heme center: Ile81 and Val83. These findings and our previous studies, which showed that hydrated water molecules around Ile81 and Val83 are expelled when Cyt c forms a complex with CcO, proposed that dehydration of these residues is functionally significant to electron transfer from Cyt c to CcO.

Keywords: Cytochrome c; Dehydration; Electron transfer; Heme.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cytochromes c / chemistry*
  • Electron Transport
  • Heme / chemistry*
  • Humans
  • Oxidation-Reduction
  • Oxygen / chemistry*
  • Polyethylene Glycols / chemistry*
  • Protein Conformation

Substances

  • Polyethylene Glycols
  • Heme
  • Cytochromes c
  • Oxygen