Edward A. Doisy Department of Biochemistry and Molecular Biology, St. Louis University School of Medicine, St. Louis, Missouri 63104, USA.
J Biol Chem. 2013 May 3;288(18):12692-8. doi: 10.1074/jbc.M113.459347. Epub 2013 Mar 25.
The two plasma inhibitors, protein Z-dependent protease inhibitor (ZPI) and tissue factor pathway inhibitor (TFPI), effectively inhibit the activity of activated factor X (FXa); however, neither inhibitor exhibits any reactivity with the homologous protease activated factor IX (FIXa). In this study, we investigated the molecular basis for the lack of reactivity of FIXa with these plasma inhibitors and discovered that unique structural features within residues of the 39-loop are responsible for restricting the inhibitor specificity of FIXa. This loop in FXa is highly acidic and contains three Glu residues at positions 36, 37, and 39. On the other hand, the loop is shorter by one residue in FIXa (residue 37 is missing), and it contains a Lys and an Asp at positions 36 and 39, respectively. We discovered that replacing residues of the 39-loop (residues 31-41) of FIXa with corresponding residues of FXa renders the FIXa chimera susceptible to inactivation by both ZPI and TFPI. Thus, the inactivation rate of the FIXa chimera by ZPI in the presence of protein Z (PZ), negatively charged membrane vesicles, and calcium ions approached the same diffusion-limited rate (>10(7) m(-1) s(-1)) that has been observed for the PZ-dependent inhibition of FXa by ZPI. Interestingly, sequence alignments indicated that, similar to FXa, residue 36 is a Glu in both mouse and bovine FIXa and that both proteases are also susceptible to inhibition by the PZ-ZPI complex. These results suggest that structural features within residues of the 39-loop contribute to the resistance of FIXa to inhibition by plasma inhibitors ZPI and TFPI.
两种血浆抑制剂,蛋白 Z 依赖性蛋白酶抑制剂(ZPI)和组织因子途径抑制剂(TFPI),能有效抑制激活的因子 X(FXa)的活性;然而,这两种抑制剂均与同源蛋白酶激活的因子 IX(FIXa)无反应性。在这项研究中,我们研究了 FIXa 与这些血浆抑制剂缺乏反应性的分子基础,并发现 39 环内独特的结构特征限制了 FIXa 对抑制剂的特异性。FXa 中的该环高度酸性,在位置 36、37 和 39 处含有三个谷氨酸残基。另一方面,FIXa 中的环短一个残基(缺失位置 37 的残基),并且在位置 36 和 39 处分别含有一个赖氨酸和天冬氨酸。我们发现,用 FXa 的相应残基替换 FIXa 的 39 环(残基 31-41)的残基,使 FIXa 嵌合体易受 ZPI 和 TFPI 的失活。因此,在蛋白 Z(PZ)、带负电荷的膜囊泡和钙离子存在下,ZPI 对 FIXa 嵌合体的失活速率接近观察到的 PZ 依赖性 ZPI 对 FXa 的抑制的相同扩散限制速率(>10(7) m(-1) s(-1))。有趣的是,序列比对表明,与 FXa 相似,36 位残基在鼠和牛 FIXa 中均为谷氨酸,并且这两种蛋白酶均易受 PZ-ZPI 复合物的抑制。这些结果表明,39 环内残基的结构特征有助于 FIXa 抵抗血浆抑制剂 ZPI 和 TFPI 的抑制。