Arbelo-Lopez Hector D, Simakov Nikolay A, Smith Jeremy C, Lopez-Garriga Juan, Wymore Troy
Chemistry Department, University of Puerto Rico , Mayagüez Campus, Mayagüez 00681, Puerto Rico.
Center for Computational Research, University of Buffalo , Buffalo, New York 14203, United States.
J Phys Chem B. 2016 Aug 4;120(30):7319-31. doi: 10.1021/acs.jpcb.6b02839. Epub 2016 Jul 22.
Many heme-containing proteins with a histidine in the distal E7 (HisE7) position can form sulfheme in the presence of hydrogen sulfide (H2S) and a reactive oxygen species such as hydrogen peroxide. For reasons unknown, sulfheme derivatives are formed specifically on solvent-excluded heme pyrrole B. Sulfhemes severely decrease the oxygen-binding affinity in hemoglobin (Hb) and myoglobin (Mb). Here, use of hybrid quantum mechanical/molecular mechanical methods has permitted characterization of the entire process of sulfheme formation in the HisE7 mutant of hemoglobin I (HbI) from Lucina pectinata. This process includes a mechanism for H2S to enter the solvent-excluded active site through a hydrophobic channel to ultimately form a hydrogen bond with H2O2 bound to Fe(III). Proton transfer from H2O2 to His64 to form compound (Cpd) 0, followed by hydrogen transfer from H2S to the Fe(III)-H2O2 complex, results in homolytic cleavage of the O-O and S-H bonds to form a reactive thiyl radical (HS(•)), ferryl heme Cpd II, and a water molecule. Subsequently, the addition of HS(•) to Cpd II, followed by three proton transfer reactions, results in the formation of a three-membered ring ferric sulfheme that avoids migration of the radical to the protein matrix, in contrast to that in other peroxidative reactions. The transformation of this three-membered episulfide ring structure to the five-membered thiochlorin ring structure occurs through a significant potential energy barrier, although both structures are nearly isoenergetic. Both three- and five-membered ring structures reveal longer NB-Fe(III) bonds compared with other pyrrole nitrogen-Fe(III) bonds, which would lead to decreased oxygen binding. Overall, these results are in agreement with a wide range of experimental data and provide fertile ground for further investigations of sulfheme formation in other heme proteins and additional effects of H2S on cell signaling and reactivity.
许多在远侧E7位含有组氨酸(HisE7)的含血红素蛋白,在硫化氢(H₂S)和活性氧(如过氧化氢)存在的情况下能够形成硫血红素。原因不明的是,硫血红素衍生物是在溶剂排除的血红素吡咯B上特异性形成的。硫血红素会严重降低血红蛋白(Hb)和肌红蛋白(Mb)中的氧结合亲和力。在这里,使用混合量子力学/分子力学方法能够对来自栉孔扇贝的血红蛋白I(HbI)的HisE7突变体中硫血红素形成的整个过程进行表征。这个过程包括H₂S通过疏水通道进入溶剂排除的活性位点,最终与结合到Fe(III)上的H₂O₂形成氢键的机制。质子从H₂O₂转移到His64形成化合物(Cpd)0,随后氢从H₂S转移到Fe(III)-H₂O₂复合物,导致O-O和S-H键的均裂,形成反应性硫自由基(HS(•))、高铁血红素Cpd II和一个水分子。随后,HS(•)添加到Cpd II上,接着进行三个质子转移反应,形成一个三元环铁硫血红素,与其他过氧化反应不同的是,该过程避免了自由基向蛋白质基质的迁移。尽管这两种结构的能量几乎相等,但这种三元环硫醚环结构向五元环硫卟啉环结构的转变会通过一个显著的势能垒。与其他吡咯氮-Fe(III)键相比,三元环和五元环结构都显示出更长的NB-Fe(III)键,这会导致氧结合能力下降。总体而言,这些结果与广泛的实验数据一致,并为进一步研究其他血红素蛋白中硫血红素的形成以及H₂S对细胞信号传导和反应性的其他影响提供了丰富的研究基础。