Crestoni Maria Elisa, Fornarini Simonetta
Dipartimento di Studi di Chimica e Tecnologia delle Sostanze Biologicamente Attive, Università di Roma La Sapienza, Piazzale A. Moro 5, Rome, Italy.
Inorg Chem. 2007 Oct 29;46(22):9018-20. doi: 10.1021/ic700698d. Epub 2007 Sep 26.
Gaseous iron protoporphyrin IX (heme) ions, Fe(PP-IX)+, obtained by electrospray ionization of a methanol solution of hemin chloride, are allowed to react with ozone, forming a species that is tentatively assigned the structure of an oxo complex, namely, an oxo iron(IV) protoporphyrin IX radical-cation species, (PP-IX).+FeIV=O. This species, representing the naked core of the putative active oxidant (compound I) of heme enzymes, is characterized by its reactivity behavior in Fourier transform ion cyclotron resonance mass spectrometry, performing as an active O-atom donor. A quite distinct reactivity is displayed by an isomeric species, holding the additional oxygen on the porphyrin frame, Fe(PP-IX(O))+. This isomer undergoes a ligand addition process, as was previously observed for Fe(PP-IX)+.
通过对氯化血红素甲醇溶液进行电喷雾电离得到的气态铁原卟啉IX(血红素)离子Fe(PP - IX)+,使其与臭氧反应,形成一种暂定为氧代配合物结构的物质,即氧代铁(IV)原卟啉IX自由基阳离子物质(PP - IX).+FeIV=O。该物质代表血红素酶假定活性氧化剂(化合物I)的裸核,通过其在傅里叶变换离子回旋共振质谱中的反应行为进行表征,表现为活性氧原子供体。一种异构体物种Fe(PP - IX(O))+表现出截然不同的反应性,其在卟啉框架上带有额外的氧。如先前对Fe(PP - IX)+所观察到的那样,这种异构体经历配体加成过程。