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调节应力激酶p38αα调节的氧化还原依赖性 conformational 开关的结构基础
Joan Pous1, Blazej Baginski1,2, Pau Martin-Malpartida1
1Institute for Research in Biomedicine (IRB Barcelona), The Barcelona Institute of Science and Technology, Baldiri Reixac, 10, 08028, Barcelona, Spain.
蛋白激酶p38α可以存在于氧化和还原状态,影响其活性. 这种氧化还原开关为设计p38α抑制剂提供了新的机会.
科学领域:
- 生物化学 生物化学
- 结构生物学 结构生物学
- 分子生物学分子生物学
背景情况:
- 存在300多个蛋白质激酶p38α的结构,主要是在减少的状态.
- 这些结构有助于了解p38α与激活剂,基质和抑制剂的相互作用.
研究的目的:
- 描述蛋白激酶p38α的氧化构造.
- 调查氧化还原状态对p38α结构和活性的功能影响.
- 为了确定用于抑制剂设计的新网站.
主要方法:
- 进行X射线晶体学以确定氧化p38α的结构.
- 氧化和减少的p38α形状的比较分析.
主要成果:
- 确定了p38α的新型氧化状态,在Cys119和Cys162.2之间具有分子内二硫化键.
- 这种氧化不会改变催化部位,而是通过影响αD螺旋来改变对接槽.
- 氧化和还原状态之间的形态变化为p38α活性提供了氧化还原依赖的微调机制.
结论:
- p38α的氧化还原状态提供了一种超出酸化的活性调节机制.
- 氧化还原状态之间的结构灵活性为p38α抑制剂的发展提供了新的裂.
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