Lloyd J R, Cotter M L, Ohori D, Doyle D L
Research Laboratories, Ortho Pharmaceutical Corporation, Raritan, New Jersey.
Biomed Environ Mass Spectrom. 1988 Apr 1;15(7):399-402. doi: 10.1002/bms.1200150707.
A fast atom bombardment/collisional activation/linked-scan at constant B/E (tandem mass spectrometric) method is described which can distinguish between alpha- and beta-aspartyl and alpha- and gamma-glutamyl underivatized peptides. The method is based upon differences in loss of CO from aspartyl or glutamyl B-fragment ions (IB) in these isomers which are rationalized from the stability of the resultant A-fragment ions (IA). It was observed that the ratio of IB:IA which was used in this determination was dependent upon the collision cell pressure. The higher the collision cell pressure, the larger the difference between the IB:IA ratios for these linkages.
描述了一种快速原子轰击/碰撞活化/在恒定B/E下的联动扫描(串联质谱)方法,该方法可区分α-和β-天冬氨酰以及α-和γ-谷氨酰未衍生化肽。该方法基于这些异构体中天冬氨酰或谷氨酰B-碎片离子(IB)损失CO的差异,这可从所得A-碎片离子(IA)的稳定性得到合理说明。据观察,此测定中使用的IB:IA比值取决于碰撞池压力。碰撞池压力越高,这些连接的IB:IA比值之间的差异就越大。