一个带有正电荷表面的静止相允许最小化移动相中的酸度,在LC-MS蛋白质原子实验中增强电喷射电离
Siddharth Jadeja1, Rudolf Kupcik2, Ivo Fabrik2
1Department of Analytical Chemistry, Faculty of Pharmacy in Hradec Králové, Charles University, Heyrovského 1203/8, 500 03 Hradec Králové, Czech Republic. lenco@faf.cuni.cz.
The Analyst
|October 23, 2023
概括
减少液态染色体质谱学 (LC-MS) 移动相中的酸可以提高的识别灵敏度. 降低甲酸度可以改善MS信号响应和用于蛋白质组分析的序列.
科学领域:
- 分析化学 分析化学
- 生物化学 生物化学
- 质谱测量质量谱测量
背景情况:
- 由于其特性,0.10%的酸是自下而上的液态染色学-质谱学 (LC-MS) 蛋白质组分析的标准移动相酸化剂.
- 现在,先进的染色体列允许高效地分离低离子强度的MS友好的移动相.
- 之前的研究还没有探讨降低酸度以提高基于MS的分析方法灵敏度.
研究的目的:
- 评估减少酸度对色谱行为和MS反应的影响.
- 为了研究使用减少的酸与具有正电荷表面的C18静止相柱的使用.
主要方法:
- 在移动阶段评估了减少的甲状酸度 (0.01%).
- 使用的柱子装有C18静止相,具有正电荷表面.
- 用各种蛋白质样本在分析流,微流和纳米流系统中进行测试.
主要成果:
- 使用0.01%的酸保持了出色的染色学性能,同时增加了MS信号响应,而0.10%相比.
- 增强的多发性硬化反应导致大约50%的标识改善,这取决于样本的复杂性和数量.
- 在较低的甲酸度下增加的基保留与酸性残留物数量直接相关.
结论:
- 在移动阶段降低甲酸度是改善LC-MS蛋白质组中的MS敏感性的可行策略.
- 这种优化提高了的识别率,适用于各种流动模式和样本类型.
- 这些发现表明在敏感蛋白质组分析中移动相组合的新标准.
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