Martin-Diaconescu Vlad, Chacón Kelly N, Delgado-Jaime Mario Ulises, Sokaras Dimosthenis, Weng Tsu-Chien, DeBeer Serena, Blackburn Ninian J
Max Planck Institute for Chemical Energy Conversion , Stiftstraße 34-36, D-45470 Mülheim an der Ruhr, Germany.
Institute of Environmental Health, Oregon Health & Sciences University , 3181 SW Sam Jackson Park Road, Portland, Oregon 97239, United States.
Inorg Chem. 2016 Apr 4;55(7):3431-9. doi: 10.1021/acs.inorgchem.5b02842. Epub 2016 Mar 11.
Biological systems use copper as a redox center in many metalloproteins, where the role of the metal is to cycle between its +1 and +2 oxidation states. This chemistry requires the redox potential to be in a range that can stabilize both Cu(I) and Cu(II) states and often involves protein-derived ligand sets involving mixed histidine-methionine coordination that balance the preferences of both oxidation states. Transport proteins, on the other hand, utilize copper in the Cu(I) state and often contain sites comprised predominately of the cuprophilic residue methionine. The electronic factors that allow enzymes and transporters to balance their redox requirements are complex and are often elusive due to the dearth of spectroscopic probes of the Cu(I) state. Here we present the novel application of X-ray emission spectroscopy to copper proteins via a study of a series of mixed His-Met copper sites where the ligand set varies in a systematic way between the His3 and Met3 limits. The sites are derived from the wild-type peptidylglycine monooxygenase (PHM), two single-site variants which replicate each of its two copper sites (CuM-site and CuH-site), and the transporters CusF and CusB. Clear differences are observed in the Kβ2,5 region at the Met3 and His3 limits. CusB (Met3) has a distinct peak at 8978.4 eV with a broad shoulder at 8975.6 eV, whereas CuH (His3) has two well-resolved features: a more intense feature at 8974.8 eV and a second at 8977.2 eV. The mixed coordination sphere CusF (Met2His) and the PHM CuM variant (Met1His2) have very similar spectra consisting of two features at 8975.2 and 8977.8 eV. An analysis of DFT calculated spectra indicate that the intensity of the higher energy peak near 8978 eV is mediated by mixing of ligand-based orbitals into the Cu d(10) manifold, with S from Met providing more intensity by facilitating increased Cu p-d mixing. Furthermore, reaction of WT PHM with CO (an oxygen analogue) produced the M site CO complex, which showed a unique XES spectrum that could be computationally reproduced by including interactions between Cu(I) and the CO ligand. The study suggests that the valence-to-core (VtC) region can not only serve as a probe of ligand speciation but also offer insight into the coordination geometry, in a fashion similar to XAS pre-edges, and may be sufficiently sensitive to the coordination of exogenous ligands to be useful in the study of reaction mechanisms.
生物系统在许多金属蛋白中使用铜作为氧化还原中心,其中金属的作用是在其+1和+2氧化态之间循环。这种化学性质要求氧化还原电位处于能够稳定Cu(I)和Cu(II)态的范围内,并且通常涉及源自蛋白质的配体组,该配体组涉及组氨酸 - 甲硫氨酸的混合配位,以平衡两种氧化态的偏好。另一方面,转运蛋白利用Cu(I)态的铜,并且通常包含主要由亲铜残基甲硫氨酸组成的位点。使酶和转运蛋白平衡其氧化还原需求的电子因素很复杂,并且由于缺乏Cu(I)态的光谱探针,这些因素常常难以捉摸。在这里,我们通过研究一系列混合的His - Met铜位点,展示了X射线发射光谱在铜蛋白中的新应用,其中配体组在His3和Met3极限之间以系统的方式变化。这些位点源自野生型肽基甘氨酸单加氧酶(PHM)、复制其两个铜位点(CuM位点和CuH位点)的两个单一位点变体以及转运蛋白CusF和CusB。在Met3和His3极限处的Kβ2,5区域观察到明显差异。CusB(Met3)在8978.4 eV处有一个明显的峰,在8975.6 eV处有一个宽肩峰,而CuH(His3)有两个分辨率良好的特征:在8974.8 eV处有一个更强的特征,在8977.2 eV处有第二个特征。混合配位球CusF(Met2His)和PHM CuM变体(Met1His2)具有非常相似的光谱,由8975.2和8977.8 eV处的两个特征组成。对DFT计算光谱的分析表明,8978 eV附近较高能量峰的强度是由基于配体的轨道混入Cu d(10)流形介导的,来自Met的S通过促进增加的Cu p - d混合提供更多强度。此外,WT PHM与CO(一种氧类似物)的反应产生了M位点CO络合物,该络合物显示出独特的XES光谱,通过包括Cu(I)与CO配体之间的相互作用可以通过计算重现。该研究表明,价到核(VtC)区域不仅可以作为配体形态的探针,还可以以类似于XAS预边缘的方式提供有关配位几何结构的见解,并且可能对外源配体的配位足够敏感,可用于反应机制的研究。