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Peptide nucleic acid and amino acid modified peptide nucleic acid analysis by capillary zone electrophoresis

机译:肽核酸和氨基酸改性肽核酸分析毛细管区电泳

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摘要

A rapid, high resolution, and low sample consumption CZE method is developed for peptide nucleic acid (PNA) analysis for the first time. 30% v/v acetonitrile in PNA sample and 20% v/v acetonitrile in 50 mM borax-boric acid (pH 8.7) as BGE were employed after optimization. The calibration curves were linear for PNA concentration ranging from 1 to 50 mu mol/L. LOD and LOQ of PNA were 0.2 and 1.0 mu mol/L, respectively. Since the commercially available reagent gives rise to huge PNA peak and an apparent impurity peak, the purity of PNA was evaluated to be about 81.4% by CZE method, obviously lower than the supplier's purity value of 99.9% evaluated by RP-HPLC, and also lower than 94.8% determined with RP-HPLC by our research group. The CZE method takes only 5 min, needs only 90 nL PNA, much less than 20 min and 20 mu L PNA in RP-HPLC method. Moreover, the CZE method is applicable for the analysis of glutamic acid modified and lysine modified PNAs, they show different migration time with their corresponding complementary PNAs. Our results show CZE provides a new choice for PNA and modified PNA analysis, also their purity or quality evaluation.
机译:首次开发了一种快速,高分辨率和低样品消耗CZE方法,用于肽核酸(PNA)分析。在优化后,使用PNA样品中30%v / v乙腈和在50mM硼酸硼酸(pH8.7)中的20%v / v乙腈作为BGE。校准曲线是线性的,用于PNA浓度范围为1至50μmmol/ l。 PNA的LOD和LOQ分别为0.2和1.0μmmol/ l。由于市售试剂引起巨大PNA峰和表观杂质峰,PNA的纯度评价为大约由CZE方法81.4%,明显高于通过RP-HPLC评价为99.9%的供应商的纯度值降低,并且还我们的研究组与RP-HPLC确定的94.8%。 CZE方法仅需5分钟,仅需要90nL PNA,rp-HPLC方法中的少于20分钟和20μl的PNA。此外,CZE方法适用于分析谷氨酸改性和赖氨酸改性PNA的分析,它们显示出不同的迁移时间与相应的互补PNA。我们的结果显示CZE为PNA和改性PNA分析提供了新的选择,也是它们的纯度或质量评估。

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