De novo design of an artificial bis[4fe-4s] binding protein

Anindya Roy, Iosifina Sarrou, Michael D. Vaughn, Andrei V. Astashkin, Giovanna Ghirlanda

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

In nature, protein subunits containing multiple iron-sulfur clusters often mediate the delivery of reducing equivalents from metabolic pathways to the active site of redox proteins. The de novo design of redox active proteins should include the engineering of a conduit for the delivery of electrons to and from the active site, in which multiple redox active centers are arranged in a controlled manner. Here, we describe a designed three-helix protein, DSD-bis[4Fe-4S], that coordinates two iron-sulfur clusters within its hydrophobic core. The design exploits the pseudo two-fold symmetry of the protein scaffold, DSD, which is a homodimeric three-helix bundle. Starting from the sequence of the parent peptide, we mutated eight leucine residues per dimer in the hydrophobic core to cysteine to provide the first coordination sphere for cubane-type iron-sulfur clusters. Incorporation of two clusters per dimer is readily achieved by in situ reconstitution and imparts increased stability to thermal denaturation compared to that of the apo form of the peptide as assessed by circular dichroism-monitored thermal denaturation. The presence of [4Fe-4S] clusters in intact proteins is confirmed by UV-vis spectroscopy, gel filtration, analytical ultracentrifugation, and electron paramagnetic resonance spectroscopy. Pulsed electron-electron double-resonance experiments have detected a magnetic dipole interaction between the two clusters ∼0.7 MHz, which is consistent with the expected intercluster distance of 29-34 Å. Taken together, our data demonstrate the successful design of an artificial multi-iron-sulfur cluster protein with evidence of cluster-cluster interaction. The design principles implemented here can be extended to the design of multicluster molecular wires.

Original languageEnglish
Pages (from-to)7586-7594
Number of pages9
JournalBiochemistry
Volume52
Issue number43
DOIs
Publication statusPublished - Oct 29 2013

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Carrier Proteins
Sulfur
Oxidation-Reduction
Iron
Electrons
Proteins
Denaturation
Catalytic Domain
Spectrum Analysis
Dimers
Hot Temperature
Iron-Sulfur Proteins
Peptides
Ultracentrifugation
Electron Spin Resonance Spectroscopy
Protein Subunits
Circular Dichroism
Metabolic Networks and Pathways
Leucine
Gel Chromatography

ASJC Scopus subject areas

  • Biochemistry

Cite this

Roy, A., Sarrou, I., Vaughn, M. D., Astashkin, A. V., & Ghirlanda, G. (2013). De novo design of an artificial bis[4fe-4s] binding protein. Biochemistry, 52(43), 7586-7594. https://doi.org/10.1021/bi401199s

De novo design of an artificial bis[4fe-4s] binding protein. / Roy, Anindya; Sarrou, Iosifina; Vaughn, Michael D.; Astashkin, Andrei V.; Ghirlanda, Giovanna.

In: Biochemistry, Vol. 52, No. 43, 29.10.2013, p. 7586-7594.

Research output: Contribution to journalArticle

Roy, A, Sarrou, I, Vaughn, MD, Astashkin, AV & Ghirlanda, G 2013, 'De novo design of an artificial bis[4fe-4s] binding protein', Biochemistry, vol. 52, no. 43, pp. 7586-7594. https://doi.org/10.1021/bi401199s
Roy, Anindya ; Sarrou, Iosifina ; Vaughn, Michael D. ; Astashkin, Andrei V. ; Ghirlanda, Giovanna. / De novo design of an artificial bis[4fe-4s] binding protein. In: Biochemistry. 2013 ; Vol. 52, No. 43. pp. 7586-7594.
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