Bera Subhadeep, Ghude Arijeet, Catalano Vincent J, Mouesca Jean-Marie, García-Serres Ricardo, Murray Leslie J
Center for Catalysis and Florida Center for Heterocyclic Chemistry, Department of Chemistry, University of Florida, Gainesville, Florida 32611, United States.
Department of Chemistry, University of Nevada, Reno, Nevada 89557, United States.
J Am Chem Soc. 2025 Jul 2;147(26):22329-22334. doi: 10.1021/jacs.5c05636. Epub 2025 Jun 16.
Nitric oxide (NO), produced by nitrite reductases or nitric oxide synthases, performs vital roles in signaling and the immune response. Iron sulfur (FeS) clusters are known targets for NO induced degradation, serving as sensors to trigger cellular responses. However, this FeS reactivity is proposed as NO specific, with no demonstrated reactivity toward nitrite, a soluble NO storage molecule. We demonstrate that synthetic FeS clusters supported by various ligands undergo facile nitrosylation by nitrite in the presence of a reductant, evidencing the nitrite reductase reactivity for FeS clusters. Moreover, a mononitrosylated FeS cluster, [tempSFeS(NO)], can be readily synthesized by this approach, enabling further investigation into the FeS cluster repair and decomposition under NO induced oxidative stress.
由亚硝酸还原酶或一氧化氮合酶产生的一氧化氮(NO)在信号传导和免疫反应中发挥着至关重要的作用。铁硫(FeS)簇是已知的NO诱导降解的靶点,可作为触发细胞反应的传感器。然而,这种FeS反应性被认为是NO特异性的,对亚硝酸盐(一种可溶性NO储存分子)没有表现出反应性。我们证明,在还原剂存在下,由各种配体支持的合成FeS簇可通过亚硝酸盐进行容易的亚硝基化,证明了FeS簇的亚硝酸还原酶反应性。此外,通过这种方法可以很容易地合成单亚硝基化的FeS簇[tempSFeS(NO)],从而能够进一步研究在NO诱导的氧化应激下FeS簇的修复和分解。