Roberts Blaine R, Tainer John A, Getzoff Elizabeth D, Malencik Dean A, Anderson Sonia R, Bomben Valerie C, Meyers Kathrin R, Karplus P Andrew, Beckman Joseph S
Department of Biochemistry and Biophysics, Oregon State University, Corvallis, OR 97331, USA.
J Mol Biol. 2007 Nov 2;373(4):877-90. doi: 10.1016/j.jmb.2007.07.043. Epub 2007 Aug 2.
Over 130 mutations to copper, zinc superoxide dismutase (SOD) are implicated in the selective death of motor neurons found in 25% of patients with familial amyotrophic lateral sclerosis (ALS). Despite their widespread distribution, ALS mutations appear positioned to cause structural and misfolding defects. Such defects decrease SOD's affinity for zinc, and loss of zinc from SOD is sufficient to induce apoptosis in motor neurons in vitro. To examine the importance of the zinc site in the structure and pathogenesis of human SOD, we determined the 2.0-A-resolution crystal structure of a designed zinc-deficient human SOD, in which two zinc-binding ligands have been mutated to hydrogen-bonding serine residues. This structure revealed a 9 degrees twist of the subunits, which opens the SOD dimer interface and represents the largest intersubunit rotational shift observed for a human SOD variant. Furthermore, the electrostatic loop and zinc-binding subloop were partly disordered, the catalytically important Arg143 was rotated away from the active site, and the normally rigid intramolecular Cys57-Cys146 disulfide bridge assumed two conformations. Together, these changes allow small molecules greater access to the catalytic copper, consistent with the observed increased redox activity of zinc-deficient SOD. Moreover, the dimer interface is weakened and the Cys57-Cys146 disulfide is more labile, as demonstrated by the increased aggregation of zinc-deficient SOD in the presence of a thiol reductant. However, equimolar Cu,Zn SOD rapidly forms heterodimers with zinc-deficient SOD (t1/2 approximately 15 min) and prevents aggregation. The stabilization of zinc-deficient SOD as a heterodimer with Cu,Zn SOD may contribute to the dominant inheritance of ALS mutations. These results have general implications for the importance of framework stability on normal metalloenzyme function and specific implications for the role of zinc ion in the fatal neuropathology associated with SOD mutations.
超过130种铜锌超氧化物歧化酶(SOD)突变与25%的家族性肌萎缩侧索硬化症(ALS)患者中运动神经元的选择性死亡有关。尽管这些突变分布广泛,但ALS突变似乎会导致结构和错误折叠缺陷。这些缺陷会降低SOD对锌的亲和力,而SOD中锌的丢失足以在体外诱导运动神经元凋亡。为了研究锌位点在人SOD结构和发病机制中的重要性,我们确定了一种设计的锌缺乏型人SOD的2.0埃分辨率晶体结构,其中两个锌结合配体已突变为氢键丝氨酸残基。该结构揭示了亚基发生9度扭转,这打开了SOD二聚体界面,代表了人SOD变体中观察到的最大亚基间旋转位移。此外,静电环和锌结合亚环部分无序,催化重要的精氨酸143从活性位点旋转开,通常刚性的分子内半胱氨酸57-半胱氨酸146二硫键呈现两种构象。这些变化共同使得小分子更容易接近催化铜,这与观察到的锌缺乏型SOD氧化还原活性增加一致。此外,二聚体界面被削弱,半胱氨酸57-半胱氨酸146二硫键更不稳定,这在硫醇还原剂存在下锌缺乏型SOD聚集增加中得到证明。然而,等摩尔的铜锌SOD能迅速与锌缺乏型SOD形成异二聚体(半衰期约15分钟)并防止聚集。锌缺乏型SOD与铜锌SOD形成异二聚体的稳定作用可能有助于ALS突变的显性遗传。这些结果对于框架稳定性对正常金属酶功能的重要性具有普遍意义,对于锌离子在与SOD突变相关的致命神经病理学中的作用具有特定意义。