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Updated: Jun 2, 2026

An Improved Method to Isolate Mitochondrial Contact Sites
Published on: June 16, 2023
The mitochondrial cytochrome c N-terminal region is critical for maturation by holocytochrome c synthase
Julie M Stevens1, Yulin Zhang, Gajanthan Muthuvel
1Department of Biochemistry, University of Oxford, Oxford, United Kingdom. julie.stevens@bioch.ox.ac.uk
Abstract:
The covalent attachment of heme to mitochondrial cytochrome c is catalysed by holocytochrome c synthase (HCCS, also called heme lyase). How HCCS functions and recognises the substrate apocytochrome is unknown. Here we have examined HCCS recognition of a chimeric substrate comprising a short mitochondrial cytochrome c N-terminal region with the C-terminal sequence, including the CXXCH heme-binding motif, of a bacterial cytochrome c that is not otherwise processed by HCCS. Heme attachment to the chimera demonstrates the importance of the N-terminal region of the cytochrome. A series of variants of a mitochondrial cytochrome c with amino acid replacements in the N-terminal region have narrowed down the specificity determinants, providing insight into HCCS substrate recognition.
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