Structure, function, and assembly of heme centers in mitochondrial respiratory complexes

Authors

Hyung J. Kim, University of Utah Health Sciences Center
Oleh Khalimonchuk, University of Nebraska-LincolnFollow
Pamela M. Smith, University of Utah Health Sciences Center
Dennis R. Winge, University of Utah Health Sciences Center

Document Type

Article

Date of this Version

2012

Citation

Biochim Biophys Acta. 2012 September ; 1823(9): 1604–1616.

Comments

© 2012 Elsevier B.V. All rights reserved.

Abstract

The sequential flow of electrons in the respiratory chain, from a low reduction potential substrate to O₂, is mediated by protein-bound redox cofactors. In mitochondria, hemes—together with flavin, iron–sulfur, and copper cofactors—mediate this multi-electron transfer. Hemes, in three different forms, are used as a protein-bound prosthetic group in succinate dehydrogenase (complex II), in bc₁ complex (complex III) and in cytochrome c oxidase (complex IV). The exact function of heme b in complex II is still unclear, and lags behind in operational detail that is available for the hemes of complex III and IV. The two b hemes of complex III participate in the unique bifurcation of electron flow from the oxidation of ubiquinol, while heme c of the cytochrome c subunit, Cyt1, transfers these electrons to the peripheral cytochrome c. The unique heme a₃, with Cu_B, form a catalytic site in complex IV that binds and reduces molecular oxygen. In addition to providing catalytic and electron transfer operations, hemes also serve a critical role in the assembly of these respiratory complexes, which is just beginning to be understood. In the absence of heme, the assembly of complex II is impaired, especially in mammalian cells. In complex III, a covalent attachment of the heme to apo-Cyt1 is a prerequisite for the complete assembly of bc₁, whereas in complex IV, heme a is required for the proper folding of the Cox 1 subunit and subsequent assembly. In this review, we provide further details of the aforementioned processes with respect to the hemes of the mitochondrial respiratory complexes.