受调节的eIF2α激酶的NO诱导的激活机制
Haruto Ishikawa1, Bo-Geon Yun, Satoshi Takahashi
1Department of Molecular Engineering, Graduate School of Engineering, Kyoto University, Kyoto 606-8501, Japan.
Journal of the American Chemical Society
|November 15, 2002
概括
氧化 (NO) 通过与其铁结合,激活受血调节的真核细胞启动因子2alpha (eIF2alpha) 激酶 (HRI). 这种激活机制涉及特定的NO-氨基酸相互作用,而不是破坏铁-基结合.
科学领域:
- 生物化学 生物化学
- 分子生物学分子生物学
- 蛋白质化学 蛋白质化学
背景情况:
- 由血红细胞调节的真核细胞启动因子2alpha (eIF2alpha) 激酶 (HRI) 在调节蛋白质合成中起着至关重要的作用,特别是在网状细胞中.
- 在HRI中含有一种N终端血结合域 (NT-HBD),可感知氧化 (NO).
研究的目的:
- 阐明NO与HRI的NT-HBD结合激活其激酶活性的分子机制.
- 要区分HRI中的NO结合机制与其他NO传感器蛋白质 (如可溶性酸环酶 (sGC)) 的 NO结合机制.
主要方法:
- 电子偏磁共振 (EPR) 光谱分析NO结合的NT-HBD.
- 共振拉曼光谱用于研究非活跃的HRI状态 (铁联体无结合和CO结合).
主要成果:
- NO与HRI的血红铁结合会产生一个六坐标复合体,与sGC中形成的五坐标复合体不同.
- 在HRI中,铁-基结合在NO结合上没有裂开,表明这不是激活触发器.
- 对HRI的CO结合也形成了六坐标复合体,表明单独的连接体替换不足以激活.
结论:
- NO诱导的HRI激活不是由于铁-基键裂解或简单的连接体替换.
- 结合NO和周围的氨基酸残留物之间的特定相互作用被认为是NO介导的HRI激活的关键机制.
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