Skeel Brighton A, Suess Daniel L M
Department of Chemistry, Massachusetts Institute of Technology, Cambridge, MA, USA.
J Biol Inorg Chem. 2025 Mar;30(2):151-159. doi: 10.1007/s00775-025-02094-0. Epub 2025 Jan 31.
Iron-sulfur proteins perform a wide variety of reactions central to the metabolisms of all living organisms. Foundational to their reaction chemistry are the rich electronic structures of their constituent Fe-S clusters, which differ in important ways from the active sites of mononuclear Fe enzymes. In this perspective, we summarize the essential electronic structure features that make Fe-S clusters unique, and point to the need for studies aimed at understanding the electronic basis for their reactivity under physiological conditions. Specifically, at ambient temperature, both the ground state and a large number of excited states are thermally populated, and thus a complete understanding of Fe-S cluster reactivity must take into account the properties, energies, and reactivity patterns of these excited states. We highlight prior research toward characterizing the low-energy excited states of Fe-S clusters that has established what is now a consensus model of these excited state manifolds and the bonding interactions that give rise to them. In particular, we discuss the low-energy alternate spin states and valence electron configurations that occur in Fe-S clusters of varying nuclearities, and finally suggest that there may be unrecognized functional roles for these states.
铁硫蛋白参与了所有生物体新陈代谢核心的多种反应。其反应化学的基础是组成它们的铁硫簇丰富的电子结构,这些电子结构在重要方面不同于单核铁酶的活性位点。从这个角度出发,我们总结了使铁硫簇独特的基本电子结构特征,并指出需要开展旨在理解其在生理条件下反应的电子基础的研究。具体而言,在环境温度下,基态和大量激发态都有热布居,因此对铁硫簇反应性的全面理解必须考虑这些激发态的性质、能量和反应模式。我们着重介绍了先前对铁硫簇低能激发态进行表征的研究,这些研究建立了目前关于这些激发态流形以及产生它们的键合相互作用的共识模型。特别是,我们讨论了不同核数的铁硫簇中出现的低能交替自旋态和价电子构型,最后提出这些状态可能存在未被认识到的功能作用。