用SAMDI质谱测量进行高通量实验的分析物无痕不移
Kazi Y Helal, Azmain Alamgir, Eric J Berns
1Department of Cell and Molecular Biology , Northwestern University Feinberg School of Medicine , Chicago , Illinois 60611 , United States.
Journal of the American Chemical Society
|June 15, 2018
概括
这项研究引入了一种无痕化学方法,用于将分子固定在表面上进行质谱分析. 这种技术避免改变分子活性,使得药物发现和反应优化的高吞吐量选成为可能.
科学领域:
- 分析化学
- 生物化学
- 有机化学
背景情况:
- 无标签的质谱测试可促进高通量反应分析.
- 目前的方法通常需要功能组来固定反应物/产物,从而可能改变分子活性.
- 在基于表面的测试中存在无痕固定技术的需求.
研究的目的:
- 开发一种无痕迹的方法,将多种分子与自组装单层 (SAM) 相对应.
- 在不改变感兴趣的分子内在性质的情况下进行基于表面的质谱分析.
- 证明这种方法在特征酶和监测化学反应中的有用性.
主要方法:
- 用3 - 三甲基-3 - - 迪亚齐林组对SAM进行功能化.
- 通过紫外线照射生成碳酸中间体.
- 碳化合物的共价插入到各种分子键中进行固定.
- 使用表面辅助激光吸附/电离 (SAMDI) 质谱法对固定 adducts 的分析.
主要成果:
- 一个成功的无痕共价固定分子到功能化的SAM.
- 通过SAMDI质谱检测固定 adducts.
- 使用该方法来表征P450药物代谢酶.
- 使用开发的技术监测木-米亚拉合反应.
结论:
- 开发的无痕固定方法对基于表面的质谱有效.
- 这种方法保留了分子的原生活性,这对于生物化学和化学研究至关重要.
- 该方法在各种科学领域具有高通量选,反应发现和优化的巨大潜力.
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