针对可调节片段的生物结合物:自由基启动的序列 (FRIPS)
Robert Hodyss1, Heather A Cox, J L Beauchamp
1Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Journal of the American Chemical Society
|September 8, 2005
概括
一种新方法使用自由基启动器在质谱仪中碎片化. 这种技术主要产生z型碎片,推进气相蛋白质测序.
科学领域:
- 质谱测量质量谱测量
- 化学分析 化学分析
- 蛋白质组学是指蛋白质组学.
背景情况:
- 粉碎对于蛋白质测序至关重要.
- 像碰撞激活解离 (CAD) 和电子捕获解离 (ECD) 这样的现有方法都有局限性.
- 开发新的碎片化技术对于促进蛋白质组学的发展至关重要.
研究的目的:
- 引入一种使用自由基启动器进行片分裂的新方法.
- 为了研究由Vazo 68-联产生的碎片化模式.
- 评估这种方法在气相蛋白质测序方面的潜力.
主要方法:
- 将自由基启动器Vazo 68与酸进行合.
- 在离子陷质谱仪中喷射结合物.
- 通过激进物种的碰撞激活诱导碎片化.
主要成果:
- 在碰撞激活时,Vazo 68-联体会产生自由基.
- 这些基因诱导骨裂变,主要形成z型碎片.
- 对 ангиотензин II-Vazo 68 结合物的分析揭示了潜在的原子抽象地点.
结论:
- 这种激进启动的碎片化方法是现有技术的可行替代方案.
- 生成的z型碎片提供了有价值的序列信息.
- 这种方法代表了迈向完全气相蛋白质测序的重要一步.
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