DeDionisio L A, Raible A M, Nelson J S
Lynx Therapeutics, Inc., Hayward, CA 94545, USA.
Electrophoresis. 1998 Nov;19(16-17):2935-8. doi: 10.1002/elps.1150191623.
N3'-->P5' phosphoramidate/phosphorothioate chimeric oligonucleotides (ODNs) are presently under investigation as potential antisense drugs. Within the field of antisense research, "second generation" chimeric ODNs have exhibited improved characteristics relative to oligonucleotides with uniformly modified backbones. The ODN of interest for this study consisted of a chemically synthesized 18-mer of mixed nucleotide base sequence with a backbone consisting of eight central phosphorothioate linkages flanked by four N3'-->P5' phosphoramidate (amidate) linkages on the 5'-end and five amidate linkages ont he 3'-end. This chimera presents analytical challenges due to the central phosphorothioate region. Here, we present a capillary gel electrophoresis (CGE) method for the analysis of the above N3'-->P5' phosphoramidate/phosphorothioate chimera. CGE was used to analyze the product prior to its purification by reversed phase - high performance liquid chromatography (RP-HPLC), and each fraction collected from the purification was similarly analyzed. An internal standard was utilized to determine the relative mobility of our product, and polyacrylamide gel electrophoresis (PAGE) analysis was used to verify CGE results.
N3'→P5'氨基磷酸酯/硫代磷酸酯嵌合寡核苷酸(ODN)目前正作为潜在的反义药物进行研究。在反义研究领域,“第二代”嵌合ODN相对于具有均匀修饰主链的寡核苷酸表现出更好的特性。本研究感兴趣的ODN由化学合成的18聚体组成,其混合核苷酸碱基序列的主链由八个中心硫代磷酸酯键组成,在5'端两侧各有四个N3'→P5'氨基磷酸酯(氨基酯)键,在3'端有五个氨基酯键。由于中心硫代磷酸酯区域,这种嵌合体带来了分析挑战。在此,我们提出一种毛细管凝胶电泳(CGE)方法来分析上述N3'→P5'氨基磷酸酯/硫代磷酸酯嵌合体。在通过反相高效液相色谱(RP-HPLC)纯化产物之前,使用CGE对其进行分析,并且对从纯化过程中收集的每个馏分进行类似的分析。使用内标来确定我们产物的相对迁移率,并使用聚丙烯酰胺凝胶电泳(PAGE)分析来验证CGE结果。