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用于多重反应监测质谱法的 b-和 y-离子的碰撞能量优化。

Collision energy optimization of b- and y-ions for multiple reaction monitoring mass spectrometry.

机构信息

Institute for Systems Biology, Seattle, Washington 98103, USA.

出版信息

J Proteome Res. 2011 Jan 7;10(1):231-40. doi: 10.1021/pr1004289. Epub 2010 Nov 22.

Abstract

Multiple reaction monitoring (MRM) is a highly sensitive and increasingly popular method of targeted mass spectrometry (MS) that can be used to selectively detect and quantify peptides and their corresponding proteins of interest within biological samples. The sensitivity of MRM-MS is highly dependent upon the tuning of transition-specific parameters, especially the collision energy (CE) applied during peptide fragmentation. Currently, empirical equations for CE work best for y-type ions and are much less effective for other types of transitions, such as b-type ions and small y-type transitions across particular amide bonds, which could also be useful for MRM-MS if optimized for maximum signal transmission. In this work, we have performed a CE optimization of all transitions for 80 doubly charged peptides, the results of which were used to define separate CE equations for b-ions and y-ions, as well as for small y-type ions derived from the fragmentation of amide bonds bounded on the amino-terminal side by aspartic or glutamic acid residues (D/E-X transitions). This analysis yielded four major observations: (1) b-ions tend to require lower collision energies than y-ions for optimal fragmentation, while D/E-X transitions tend to require more; (2) CE equations predict the optimal CEs more closely when product ion m/z dependence is included, in addition to the current standard of precursor ion m/z dependence; (3) separate CE equations for y-ions, b-ions, and D/E-X transitions are more effective than the previous one-size-fits-all equations, but best results are achieved by optimizing transitions individually; and (4) while b-ions gain substantial signal from CE optimization-often increases of several-fold-they still tend to rank lower than y-ions from the same peptide. These results confirm the notion that y-ions are usually the first-choice transitions for MRM experiments but also demonstrate, for the first time, that b-ions can be viable targets as well, if the proper collision energies are used.

摘要

多反应监测 (MRM) 是一种高度敏感且日益流行的靶向质谱 (MS) 方法,可用于选择性检测和定量生物样品中的肽及其相应的感兴趣蛋白。MRM-MS 的灵敏度高度依赖于特定转换参数的调整,特别是在肽片段化过程中应用的碰撞能 (CE)。目前,CE 的经验公式最适合 y 型离子,而对其他类型的转换(如 b 型离子和特定酰胺键上的小 y 型转换)的效果要差得多,如果优化为最大信号传输,则这些转换也可能对 MRM-MS 有用。在这项工作中,我们对 80 个双电荷肽的所有转换进行了 CE 优化,结果用于为 b 离子和 y 离子以及由天冬氨酸或谷氨酸残基(D/E-X 转换)侧酰胺键片段化而来的小 y 型离子定义单独的 CE 方程。这项分析得出了四个主要观察结果:(1) b 离子的最佳片段化所需的碰撞能通常低于 y 离子,而 D/E-X 转换则需要更多;(2) 当除了当前的前体离子 m/z 依赖性标准外,还包括产物离子 m/z 依赖性时,CE 方程更能准确预测最佳 CE;(3) y 离子、b 离子和 D/E-X 转换的单独 CE 方程比以前的一刀切方程更有效,但通过单独优化转换可以获得最佳结果;(4) 虽然 b 离子通过 CE 优化会获得大量信号——通常会增加几倍——但它们的排名仍低于来自同一肽的 y 离子。这些结果证实了 y 离子通常是 MRM 实验的首选转换的观点,但也首次表明,如果使用适当的碰撞能,b 离子也可以成为可行的目标。

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