Brandstetter H, Bauer M, Huber R, Lollar P, Bode W
Max-Planck-Institut für Biochemie, Martinsried, Germany.
Proc Natl Acad Sci U S A. 1995 Oct 10;92(21):9796-800. doi: 10.1073/pnas.92.21.9796.
Hereditary deficiency of factor IXa (fIXa), a key enzyme in blood coagulation, causes hemophilia B, a severe X chromosome-linked bleeding disorder afflicting 1 in 30,000 males; clinical studies have identified nearly 500 deleterious variants. The x-ray structure of porcine fIXa described here shows the atomic origins of the disease, while the spatial distribution of mutation sites suggests a structural model for factor X activation by phospholipid-bound fIXa and cofactor VIIIa. The 3.0-A-resolution diffraction data clearly show the structures of the serine proteinase module and the two preceding epidermal growth factor (EGF)-like modules; the N-terminal Gla module is partially disordered. The catalytic module, with covalent inhibitor D-Phe-1I-Pro-2I-Arg-3I chloromethyl ketone, most closely resembles fXa but differs significantly at several positions. Particularly noteworthy is the strained conformation of Glu-388, a residue strictly conserved in known fIXa sequences but conserved as Gly among other trypsin-like serine proteinases. Flexibility apparent in electron density together with modeling studies suggests that this may cause incomplete active site formation, even after zymogen, and hence the low catalytic activity of fIXa. The principal axes of the oblong EGF-like domains define an angle of 110 degrees, stabilized by a strictly conserved and fIX-specific interdomain salt bridge. The disorder of the Gla module, whose hydrophobic helix is apparent in electron density, can be attributed to the absence of calcium in the crystals; we have modeled the Gla module in its calcium form by using prothrombin fragment 1. The arched module arrangement agrees with fluorescence energy transfer experiments. Most hemophilic mutation sites of surface fIX residues occur on the concave surface of the bent molecule and suggest a plausible model for the membrane-bound ternary fIXa-FVIIIa-fX complex structure: fIXa and an equivalently arranged fX arch across an underlying fVIIIa subdomain from opposite sides; the stabilizing fVIIIa interactions force the catalytic modules together, completing fIXa active site formation and catalytic enhancement.
凝血因子IXa(fIXa)是血液凝固中的关键酶,其遗传性缺乏会导致B型血友病,这是一种严重的X染色体连锁出血性疾病,每30000名男性中就有1人患病;临床研究已鉴定出近500种有害变体。本文描述的猪fIXa的X射线结构揭示了该疾病的原子起源,而突变位点的空间分布则为磷脂结合的fIXa和辅因子VIIIa激活因子X提供了一个结构模型。3.0埃分辨率的衍射数据清晰地显示了丝氨酸蛋白酶模块以及前面两个表皮生长因子(EGF)样模块的结构;N端的Gla模块部分无序。催化模块与共价抑制剂D-Phe-1I-Pro-2I-Arg-3I氯甲基酮结合,与fXa最为相似,但在几个位置有显著差异。特别值得注意的是Glu-388的紧张构象,该残基在已知的fIXa序列中严格保守,但在其他胰蛋白酶样丝氨酸蛋白酶中保守为甘氨酸。电子密度中明显的灵活性以及建模研究表明,即使在酶原之后,这也可能导致活性位点形成不完全,从而导致fIXa的催化活性较低。长方形EGF样结构域的主轴定义了一个110度的角,由一个严格保守且fIX特异性的结构域间盐桥稳定。Gla模块的无序,其疏水螺旋在电子密度中明显可见,可归因于晶体中缺乏钙;我们通过使用凝血酶原片段1对其钙形式的Gla模块进行了建模。拱形的模块排列与荧光能量转移实验一致。表面fIX残基的大多数血友病突变位点位于弯曲分子的凹面上,并为膜结合的三元fIXa-FVIIIa-fX复合物结构提供了一个合理的模型:fIXa和一个等效排列的fX从相对两侧跨过潜在的FVIIIa亚结构域形成拱形;稳定的FVIIIa相互作用将催化模块聚集在一起,完成fIXa活性位点的形成并增强催化作用。