Probing a complex of cytochrome c and cardiolipin by magnetic circular dichroism spectroscopy: implications for the initial events in apoptosis

J Am Chem Soc. 2011 Dec 14;133(49):19676-9. doi: 10.1021/ja209144h. Epub 2011 Nov 18.

Abstract

Oxidation of cardiolipin (CL) by its complex with cytochrome c (cyt c) plays a crucial role in triggering apoptosis. Through a combination of magnetic circular dichroism spectroscopy and potentiometric titrations, we show that both the ferric and ferrous forms of the heme group of a CL:cyt c complex exist as multiple conformers at a physiologically relevant pH of 7.4. For the ferric state, these conformers are His/Lys- and His/OH(-)-ligated. The ferrous state is predominantly high-spin and, most likely, His/-. Interconversion of the ferric and ferrous conformers is described by a single midpoint potential of -80 ± 9 mV vs SHE. These results suggest that CL oxidation in mitochondria could occur by the reaction of molecular oxygen with the ferrous CL:cyt c complex in addition to the well-described reaction of peroxides with the ferric form.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis*
  • Cardiolipins / chemistry
  • Cardiolipins / metabolism*
  • Circular Dichroism
  • Cytochromes c / chemistry
  • Cytochromes c / metabolism*
  • Heme / chemistry
  • Heme / metabolism
  • Horses
  • Models, Molecular
  • Oxidation-Reduction
  • Potentiometry
  • Protein Binding
  • Protein Conformation

Substances

  • Cardiolipins
  • Heme
  • Cytochromes c