Unusual structures and unknown roles of FeS clusters in metalloenzymes seen from a resonance Raman spectroscopic perspective

[Display omitted] •Unusual, non-conventional FeS clusters are continuously emerging in metalloenzymes.•RR spectroscopy provides insights into electronic structures of FeS clusters.•RR spectroscopy has identified unique catalytic intermediates in hydrogenases.•RR spectroscopy allows elucidation of Fe...

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Veröffentlicht in:Coordination chemistry reviews 2022-02, Vol.452, p.214287, Article 214287
Hauptverfasser: Caserta, Giorgio, Zuccarello, Lidia, Barbosa, Catarina, Silveira, Célia M., Moe, Elin, Katz, Sagie, Hildebrandt, Peter, Zebger, Ingo, Todorovic, Smilja
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Sprache:eng
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Zusammenfassung:[Display omitted] •Unusual, non-conventional FeS clusters are continuously emerging in metalloenzymes.•RR spectroscopy provides insights into electronic structures of FeS clusters.•RR spectroscopy has identified unique catalytic intermediates in hydrogenases.•RR spectroscopy allows elucidation of FeS cluster composition in radical-SAM enzymes.•RR spectroscopy reveals insights into the role of FeS clusters in DNA repair enzymes. The universe of known biological FeS clusters is constantly enlarging. Besides the conventional, well described [2Fe–2S], [3Fe–4S] and cubane [4Fe–4S] clusters, novel, unprecedented structures are emerging. They include unusually coordinated clusters, with additional sulfur atoms, e.g., [4Fe–5S], [5Fe–5S], [4Fe–4S]-5S-[4Fe–4S], [8Fe–7S], [8Fe–9S] and [8Fe–8S–C] and heteronuclear clusters, e.g., [Ni–4Fe–4S], [2Ni–4Fe–4S], [4Fe–4S]-[2Ru], [Me–7Fe–9S–C–(homocitrate)] that undertake versatile physiological roles in the activation of small molecules (H2, CO2, CO and N2) and in the sulfuration of different compounds (e.g., t-RNAs, biotin and lipoic acid) in biology. A few structures are characterized by highly distorted geometries, e.g., the non-cubane [4Fe–4S] center and the hydrogenase-related [4Fe–3S] cluster, and contain atypical ligations or vacant coordination sites, which confer them novel functions far from the common electron transfer. Herein, we single out clusters found in i) hydrogenases that ensure sustainable hydrogen cycling, promising a clean fuel production in the future, ii) radical-SAM enzymes that can inspire applied catalysis due to an intrinsic flexibility of the radical chemistry, and iii) standard [4Fe–4S] cluster with still unknown function in DNA repair enzymes, which offer a possibility to interfere with DNA repair in pathogens or improve it in humans. Focusing on the abovementioned enzymes, we demonstrate the unique power of resonance Raman spectroscopy to unveil remarkable features in FeS centers, which has contributed to our understanding of unusual structures and disentangling of unknown functions.
ISSN:0010-8545
1873-3840
DOI:10.1016/j.ccr.2021.214287