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通过与4-氟-7-硝基-2,1,3-苯并恶二唑进行在线衍生化,对毛细管电泳中的肽和氨基酸进行荧光检测。

Fluorescent detection of peptides and amino acids for capillary electrophoresis via on-line derivatization with 4-fluoro-7-nitro-2,1,3-benzoxadiazole.

作者信息

Zhang Hongyi, Le Potier Isabelle, Smadja Claire, Zhang Jiyou, Taverna Myriam

机构信息

College of Chemistry and Environmental Science, Hebei University, Baoding 071002, People's Republic of China.

出版信息

Anal Bioanal Chem. 2006 Nov;386(5):1387-94. doi: 10.1007/s00216-006-0709-6. Epub 2006 Sep 5.

Abstract

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.

摘要

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。

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