Dec 1, 1975

Cytochrome c interaction with membranes. Absorption and emission spectra and binding characteristics of iron-free cytochrome c

European Journal of Biochemistry
J M Vanderkooi, M Erecińska

Abstract

A cytochrome c derivative from which iron is removed has been prepared and characterized. Several lines of evidence indicate that native and porphyrin cytochrome c have similar conformations: they have similar elution characteristics on Sephadex gel chromatography; in both proteins the tryptophan fluorescence is quenched and the pK values of protonation of the porphyrin are identical. Porphyrin cytochrome c does not substitute for native cytochrome c in either the oxidase reaction or in restoring electron transport in cytochrome-c-depleted mitochondria. It does however competitively inhibit native cytochrome c in these reactions, the Ki for inhibition being larger than the Km for reaction. The absorption and emission spectra, and the polarized excitation spectrum of the porphyrin cytochrome c are characteristic of free base porphyrin. The absence of fluorescence quenching of porphyrin cytochrome c when the protein is bound to cytochrome oxidase suggests that heme to heme distance between these proteins is larger than 0.5 to 0.9 nm depending upon orientation. Binding of the porphyrin cytochrome c to phospholipids or to mitochondria increases the fluorescence polarization of a positively polarized absorption band, which indicates...Continue Reading

Mentioned in this Paper

CYCS
Tryptophan
Cytochrome C Oxidase
Tissue Membrane
Energy Transfer
Oxidase
Electron Transport
Myocardium
Mitochondria, Liver
Cytochrome c Group

About this Paper

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