Department of Molecular Bacteriology, Research Institute for Microbial Diseases, Osaka University, Suita, Osaka, Japan.
The Research Foundation for Microbial Diseases of Osaka University (BIKEN), Suita, Osaka, Japan.
Microbiol Immunol. 2020 Aug;64(8):570-573. doi: 10.1111/1348-0421.12799. Epub 2020 Jul 2.
An autotransporter of Bordetella pertussis, virulence-associated gene 8 (Vag8), binds and inactivates the complement regulator, C1 inhibitor (C1-Inh), and plays a role in evasion of the complement system. However, the molecular interaction between Vag8 and C1-Inh remains unclear. Here, we localized the minimum region of Vag8 required for interaction with C1-Inh by examining the differently truncated Vag8 derivatives for the ability to bind and inactivate C1-Inh. The truncated Vag8 containing amino-acid residues 102-548, but not 102-479 and 202-648, showed the full activity of intact Vag8, suggesting that the separate 102-202 and 548-648 amino-acid regions of Vag8 mediate the interaction with C1-Inh.
百日咳博德特氏菌的一种自转运蛋白,毒力相关基因 8(Vag8),可结合并失活补体调节蛋白,C1 抑制剂(C1-Inh),并在逃避补体系统中发挥作用。然而,Vag8 与 C1-Inh 之间的分子相互作用仍不清楚。在这里,我们通过检查不同截断的 Vag8 衍生物与 C1-Inh 结合和失活的能力,定位了与 C1-Inh 相互作用所需的 Vag8 的最小区域。含有氨基酸残基 102-548 的截断 Vag8,但不含有 102-479 和 202-648 的 Vag8,显示出完整 Vag8 的全部活性,表明 Vag8 的单独 102-202 和 548-648 氨基酸区域介导与 C1-Inh 的相互作用。