首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >High-throughput purification of double-stranded RNA molecules using convective interaction media monolithic anion exchange columns
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High-throughput purification of double-stranded RNA molecules using convective interaction media monolithic anion exchange columns

机译:对流相互作用介质整体式阴离子交换柱高通量纯化双链RNA分子

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Recent advances in the field of RNA interference and new cost-effective approaches for large-scale double-stranded RNA (dsRNA) synthesis have fuelled the demand for robust high-performance purification techniques suitable for dsRNA molecules of various lengths. To address this issue, we developed an improved dsRNA purification method based on anion exchange chromatography utilizing convective interaction media (CIM) monolithic columns. To evaluate column performance we synthesized a selection of dsRNA molecules (58-1810. bp) in a one-step enzymatic reaction involving bacteriophage T7 DNA-dependent RNA polymerase and phi6 RNA-dependent RNA polymerase. In addition, small interfering RNAs (siRNAs) of 25-27. bp were generated by Dicer digestion of the genomic dsRNA of bacteriophage phi6. We demonstrated that linearly scalable CIM monolithic quaternary amine (QA) columns can be used as a fast and superior alternative to standard purification methods (e.g. LiCl precipitation) to obtain highly pure dsRNA preparations. The impurities following Dicer treatment were quickly and efficiently removed with the QA CIM monolithic column, yielding siRNA molecules of high purity suitable for potential therapeutic applications. Moreover, baseline separation of dsRNA molecules up to 1. kb in non-denaturing conditions was achieved.
机译:RNA干扰领域的最新进展以及大规模双链RNA(dsRNA)合成的新成本有效方法,激发了对适用于各种长度dsRNA分子的稳健高性能纯化技术的需求。为解决此问题,我们开发了一种改进的基于对流相互作用介质(CIM)整体柱的阴离子交换色谱法的dsRNA纯化方法。为了评估色谱柱性能,我们在涉及噬菌体T7 DNA依赖性RNA聚合酶和phi6 RNA依赖性RNA聚合酶的一步式酶促反应中合成了dsRNA分子(58-1810。bp)。此外,还有25-27的小干扰RNA(siRNA)。通过Dicer消化噬菌体phi6的基因组dsRNA产生bp。我们证明了线性可扩展的CIM整体式季胺(QA)色谱柱可以用作标准纯化方法(例如LiCl沉淀)的快速和优异替代品,以获得高纯度的dsRNA制备物。使用QA CIM整体式色谱柱可快速,有效地去除Dicer处理后的杂质,从而得到适合潜在治疗应用的高纯度siRNA分子。此外,在非变性条件下,可实现高达1. kb的dsRNA分子的基线分离。

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