Zhang Hongyi, Le Potier Isabelle, Smadja Claire, Zhang Jiyou, Taverna Myriam
College of Chemistry and Environmental Science, Hebei University, Baoding 071002, People's Republic of China.
Anal Bioanal Chem. 2006 Nov;386(5):1387-94. doi: 10.1007/s00216-006-0709-6. Epub 2006 Sep 5.
An in-capillary derivatization of amino acids and peptides with 4-fluoro-7-nitro-2,1,3-benzoxadiazole (NBD-F) was developed for their subsequent capillary electrophoretic analysis with laser-induced fluorescence detection (lambda (ex)=488 nm). The in-capillary derivatization was achieved in zone-passing mode by introducing successive plugs of sample and NBD-F into a fused silica capillary previously equilibrated with an alkaline borate buffer. To prevent NBD-F hydrolysis and to achieve a reliable derivatization, NBD-F was prepared daily in absolute ethanol and a plug of absolute ethanol was introduced between the sample and NBD-F reagent plugs. Various parameters influencing the derivatization efficiency were investigated and the optimum conditions were as follows: background electrolyte (BGE), 20 mM borate buffer (pH 8.8); introduction time, 4 s for sample and 2 s for NBD-F; molar ratio of NBD-F/sample, above 215; temperature, 45 degrees C for amino acids and 35 degrees C for peptides; applied voltage, +15 kV. The validation of the in-capillary derivatization method under optimal conditions showed a good linearity between the heights of the derivative peaks and the concentrations of the amino acids. The intra-day relative standard deviations of the migration times and the peak heights were less than 1.3% and 4.6%, respectively. The efficient derivatization and separation of a mixture of valine, alanine, glutamic acid and aspartic acid were achieved using this technique. Peptides such as buccaline and beta-protein fragment 1-42 could also be derivatized using the developed in-capillary derivatization procedure.
开发了一种用4-氟-7-硝基-2,1,3-苯并恶二唑(NBD-F)对氨基酸和肽进行毛细管内衍生化的方法,用于随后通过激光诱导荧光检测(激发波长λ = 488 nm)进行的毛细管电泳分析。通过将连续的样品和NBD-F塞子引入预先用碱性硼酸盐缓冲液平衡的熔融石英毛细管中,以区带通过模式实现毛细管内衍生化。为防止NBD-F水解并实现可靠的衍生化,NBD-F每天用无水乙醇配制,并在样品和NBD-F试剂塞子之间引入一塞无水乙醇。研究了影响衍生化效率的各种参数,最佳条件如下:背景电解质(BGE),20 mM硼酸盐缓冲液(pH 8.8);进样时间,样品4 s,NBD-F 2 s;NBD-F/样品的摩尔比,高于215;温度,氨基酸为45℃,肽为35℃;施加电压,+15 kV。在最佳条件下对毛细管内衍生化方法的验证表明,衍生化峰高与氨基酸浓度之间具有良好的线性关系。迁移时间和峰高的日内相对标准偏差分别小于1.3%和4.6%。使用该技术实现了缬氨酸、丙氨酸、谷氨酸和天冬氨酸混合物的高效衍生化和分离。使用所开发的毛细管内衍生化程序,也可以对诸如颊肌素和β-蛋白片段1-42等肽进行衍生化。