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Heme-containing integral membrane proteins are at the heart of many bioenergetic complexes and electron transport chains. The importance of these electron relay hubs across biology has inspired the design of de novo proteins that recreate their core features within robust, versatile, and tractable protein folds. To this end, we report here the computational design and in-cell production of a minimal diheme membrane cytochrome which successfully integrates into the cellular membrane of live bacteria. This synthetic construct emulates a four-helix bundle found in modern respiratory complexes but has no sequence homology to any polypeptide sequence found in nature. The two b-type hemes, which appear to be recruited from the endogenous heme pool, have distinct split redox potentials with values close to those of natural membrane-spanning cytochromes. The purified protein can engage in rapid biomimetic electron transport with small molecules, with other redox proteins, and with biologically relevant diffusive electron carriers. We thus report an artificial membrane metalloprotein with the potential to serve as a functional electron transfer module in both synthetic protocells and living systems.

Original publication

DOI

10.1073/pnas.2300137120

Type

Journal article

Journal

Proceedings of the National Academy of Sciences of the United States of America

Publication Date

04/2023

Volume

120

Addresses

School of Biochemistry, University of Bristol, Bristol BS8 1TD, United Kingdom.

Keywords

Heme, Cytochromes, Metalloproteins, Electron Transport, Oxidation-Reduction