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Protein-Assisted Formation of Molybdenum Heterometallic Clusters: Evidence for the Formation of S<sub>2</sub>MoS<sub>2</sub>–M–S<sub>2</sub>MoS<sub>2</sub> Clusters with M = Fe, Co, Ni, Cu, or Cd within the Orange Protein

17

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29

References

2017

Year

Abstract

The Orange Protein (ORP) is a small bacterial protein, of unknown function, that harbors a unique molybdenum/copper (Mo/Cu) heterometallic cluster, [S<sub>2</sub>Mo<sup>VI</sup>S<sub>2</sub>Cu<sup>I</sup>S<sub>2</sub>Mo<sup>VI</sup>S<sub>2</sub>]<sup>3-</sup>, noncovalently bound. The apo-ORP is able to promote the formation and stabilization of this cluster, using Cu<sup>II</sup>- and Mo<sup>VI</sup>S<sub>4</sub><sup>2-</sup> salts as starting metallic reagents, to yield a Mo/Cu-ORP that is virtually identical to the native ORP. In this work, we explored the ORP capability of promoting protein-assisted synthesis to prepare novel protein derivatives harboring molybdenum heterometallic clusters containing iron, cobalt, nickel, or cadmium in place of the "central" copper (Mo/Fe-ORP, Mo/Co-ORP, Mo/Ni-ORP, or Mo/Cd-ORP). For that, the previously described protein-assisted synthesis protocol was extended to other metals and the Mo/M-ORP derivatives (M = Cu, Fe, Co, Ni, or Cd) were spectroscopically (UV-visible and electron paramagnetic resonance (EPR)) characterized. The Mo/Cu-ORP and Mo/Cd-ORP derivatives are stable under oxic conditions, while the Mo/Fe-ORP, Mo/Co-ORP, and Mo/Ni-ORP derivatives are dioxygen-sensitive and stable only under anoxic conditions. The metal and protein quantification shows the formation of 2Mo:1M:1ORP derivatives, and the visible spectra suggest that the expected {S<sub>2</sub>MoS<sub>2</sub>MS<sub>2</sub>MoS<sub>2</sub>} complexes are formed. The Mo/Cu-ORP, Mo/Co-ORP, and Mo/Cd-ORP are EPR-silent. The Mo/Fe-ORP derivative shows an EPR S = <sup>3</sup>/<sub>2</sub> signal (E/D ≈ 0.27, g ≈ 5.3, 2.5, and 1.7 for the lower M= ±<sup>1</sup>/<sub>2</sub> doublet, and g ≈ 5.7 and 1.7 (1.3 predicted) for the upper M = ±<sup>3</sup>/<sub>2</sub> doublet), consistent with the presence of either one S = <sup>5</sup>/<sub>2</sub> Fe<sup>III</sup> antiferromagnetically coupled to two S = <sup>1</sup>/<sub>2</sub> Mo<sup>V</sup> or one S = <sup>3</sup>/<sub>2</sub> Fe<sup>I</sup> and two S = 0 Mo<sup>VI</sup> ions, in both cases in a tetrahedral geometry. The Mo/Ni-ORP shows an EPR axial S = <sup>1</sup>/<sub>2</sub> signal consistent with either one S = <sup>1</sup>/<sub>2</sub> Ni<sup>I</sup> and two S = 0 Mo<sup>VI</sup> or one S = <sup>1</sup>/<sub>2</sub> Ni<sup>III</sup> antiferromagnetically coupled to two S = <sup>1</sup>/<sub>2</sub> Mo<sup>V</sup> ions, in both cases in a square-planar geometry. The Mo/Cu-ORP and Mo/Cd-ORP are described as {Mo<sup>VI</sup>-Cu<sup>I</sup>-Mo<sup>VI</sup>} and {Mo<sup>VI</sup>-Cd<sup>II</sup>-Mo<sup>VI</sup>}, respectively, while the other derivatives are suggested to exist in at least two possible electronic structures, {Mo<sup>VI</sup>-M<sup>I</sup>-Mo<sup>VI</sup>} ↔ {Mo<sup>V</sup>-M<sup>III</sup>-Mo<sup>V</sup>}.

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