Petritis Konstantinos, Brussaux Sylvain, Guenu Sophie, Elfakire Claire, Dreux Michel
Institut de Chimie Organique et Analytique, CNRS UMR-6005, Université d'Orléans, France.
J Chromatogr A. 2002 May 31;957(2):173-85. doi: 10.1016/s0021-9673(02)00372-2.
The single run analysis of 23 small peptides (principally glycyl and lysyl dipeptides) is performed by ion-pair reversed-phase liquid chromatography coupled with evaporative light scattering detection or electrospray (tandem) mass spectrometry. Several perfluorinated carboxylic acid homologues are evaluated with an octadecyl silica stationary phase (Supelcosil ABZ+ Plus). Among the perfluorocarboxylic acids tested the nonafluoropentanoic acid and the tridecafluoroheptanoic acid gave the best results. Special attention was paid to the separation of isomer/isobar dipeptides (e.g., Gly-Ile, Gly-Leu, Leu-Gly, as well as Gly-Gln, Gly-Lys, etc.) which is usually necessary in spite of the high specificity of mass spectrometry. Before LC-MS analysis, ion-spray fragmentation as well as optimization of MS parameters of the analysed peptides was investigated. The optimum collision energy of glysyl peptides, Ala-Gln, Asp-Asp and Asp-Asp-Asp (13-18 eV) was different from that of the lysyl peptides, Tyr-Glu and oxidised glutathione (25-32 eV). Limits of detection varied from 0.1 to 1.2 mg l(-1) for simple MS and 0.05 to 25 mg l(-1) for tandem MS.
通过离子对反相液相色谱结合蒸发光散射检测或电喷雾(串联)质谱法对23种小肽(主要是甘氨酰和赖氨酰二肽)进行单次运行分析。使用十八烷基硅胶固定相(Supelcosil ABZ+ Plus)评估了几种全氟羧酸同系物。在所测试的全氟羧酸中,九氟戊酸和十三氟庚酸给出了最佳结果。特别关注了异构体/等压二肽(例如,甘氨酰-异亮氨酸、甘氨酰-亮氨酸、亮氨酰-甘氨酸,以及甘氨酰-谷氨酰胺、甘氨酰-赖氨酸等)的分离,尽管质谱具有高特异性,但这种分离通常是必要的。在液相色谱-质谱分析之前,研究了离子喷雾碎片化以及所分析肽段的质谱参数优化。甘氨酰肽段、丙氨酰-谷氨酰胺、天冬氨酰-天冬氨酸和天冬氨酰-天冬氨酰-天冬氨酸(13 - 18电子伏特)的最佳碰撞能量与赖氨酰肽段、酪氨酰-谷氨酸和氧化型谷胱甘肽(25 - 32电子伏特)的不同。简单质谱的检测限在0.1至1.2毫克/升之间,串联质谱的检测限在0.05至25毫克/升之间。