Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, Michigan, USA.
Department of Molecular, Cellular and Developmental Biology, University of Michigan, Ann Arbor, Michigan, USA
mBio. 2020 Jul 28;11(4):e01017-20. doi: 10.1128/mBio.01017-20.
Maintaining cellular iron homeostasis is critical for organismal survival. Whereas iron depletion negatively affects the many metabolic pathways that depend on the activity of iron-containing enzymes, any excess of iron can cause the rapid formation of highly toxic reactive oxygen species (ROS) through Fenton chemistry. Although several cellular iron chelators have been identified, little is known about if and how organisms can prevent the Fenton reaction. By studying the effects of cisplatin, a commonly used anticancer drug and effective antimicrobial, we discovered that cisplatin elicits severe iron stress and oxidative DNA damage in bacteria. We found that both of these effects are successfully prevented by polyphosphate (polyP), an abundant polymer consisting solely of covalently linked inorganic phosphates. Subsequent and studies revealed that polyP provides a crucial iron reservoir under nonstress conditions and effectively complexes free iron and blocks ROS formation during iron stress. These results demonstrate that polyP, a universally conserved biomolecule, plays a hitherto unrecognized role as an iron chelator and an inhibitor of the Fenton reaction. How do organisms deal with free iron? On the one hand, iron is an essential metal that plays crucial structural and functional roles in many organisms. On the other hand, free iron is extremely toxic, particularly under aerobic conditions, where iron rapidly undergoes the Fenton reaction and produces highly reactive hydroxyl radicals. Our study now demonstrates that we have discovered one of the first physiologically relevant nonproteinaceous iron chelators and Fenton inhibitors. We found that polyphosphate, a highly conserved and ubiquitous inorganic polyanion, chelates iron and, through its multivalency, prevents the interaction of iron with peroxide and therefore the formation of hydroxyl radicals. We show that polyP provides a crucial iron reservoir for metalloproteins under nonstress conditions and effectively chelates free iron during iron stress. Importantly, polyP is present in all cells and organisms and hence is likely to take on this crucial function in both prokaryotic and eukaryotic cells.
维持细胞内铁稳态对生物的生存至关重要。铁的缺乏会对依赖含铁酶活性的许多代谢途径产生负面影响,而任何过量的铁都会通过芬顿化学快速形成高毒性的活性氧(ROS)。尽管已经鉴定出几种细胞内铁螯合剂,但对于生物体是否以及如何能够防止芬顿反应知之甚少。通过研究顺铂(一种常用的抗癌药物和有效的抗菌药物)的影响,我们发现顺铂在细菌中引发严重的铁应激和氧化 DNA 损伤。我们发现,多聚磷酸盐(polyP)可以成功预防这两种效应,polyP 是一种仅由共价连接的无机磷酸盐组成的丰富聚合物。随后的研究揭示了 polyP 在非应激条件下提供了一个关键的铁库,并在铁应激期间有效地螯合游离铁并阻止 ROS 形成。这些结果表明,polyP 作为一种普遍保守的生物分子,在作为铁螯合剂和芬顿反应抑制剂方面发挥了迄今为止尚未被认识的作用。生物体如何处理游离铁?一方面,铁是一种必需的金属,在许多生物体中发挥着至关重要的结构和功能作用。另一方面,游离铁极其有毒,特别是在有氧条件下,铁会迅速发生芬顿反应并产生高反应性的羟基自由基。我们的研究现在表明,我们已经发现了第一个具有生理相关性的非蛋白质类铁螯合剂和芬顿抑制剂之一。我们发现,多聚磷酸盐是一种高度保守且普遍存在的无机多阴离子,它可以螯合铁,并通过多价性防止铁与过氧化物相互作用,从而阻止羟基自由基的形成。我们表明,在非应激条件下,polyP 为金属蛋白提供了一个关键的铁库,并在铁应激期间有效地螯合游离铁。重要的是,polyP 存在于所有细胞和生物体中,因此很可能在原核和真核细胞中都具有这一关键功能。