Synthesis of short DNA and RNA fragments by resonant acoustic mixing (RAM)†

James D. Thorpe, Julian Marlyn, Stefan G. Koenig and Masad J. Damha
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Abstract

We demonstrate the first use of Resonant Acoustic Mixing (RAM) without bulk solvent for the synthesis of short oligonucleotide fragments. Using the modified H-phosphonate approach, DNA, RNA, and 2′-modified nucleotides were successfully coupled to 3′-protected nucleosides in high yields (63–92%) while reducing solvent volume by 90%. In addition to synthesizing protected phosphodiester (PO) dimers and trimers, we also synthesized protected phosphorothioate (PS) dimers in good yields (63–65%). Using phosphoramidite chemistry, we were similarly able to reduce the solvent volume by 90% while coupling DNA phosphoramidites (58–92%) and RNA phosphoramidites (55–95%) with 3′-protected nucleosides in high yields followed by traditional oxidation with iodine in solution. Both strategies were successfully scaled up to multi-gram quantities which was facilitated by the use of RAM, offering the potential for larger scale-up, up to hundreds of kilograms continuously.

Abstract Image

通过共振声混合 (RAM) † 合成短 DNA 和 RNA 片段
我们首次在不使用大量溶剂的情况下将共振声学混合(RAM)用于合成短寡核苷酸片段。利用改良的 H-膦酸盐方法,DNA、RNA 和 2′-修饰核苷酸成功地与 3′-保护核苷酸偶联,产率高达 63-92%,同时溶剂体积减少了 90%。除了合成受保护的磷酸二酯(PO)二聚体和三聚体外,我们还合成了受保护的硫代磷酸酯(PS)二聚体,收率高达 63-65%。利用亚磷酰胺化学,我们同样能够将溶剂体积减少 90%,同时将 DNA 亚磷酰胺(58-92%)和 RNA 亚磷酰胺(55-95%)与 3′保护核苷进行高产率偶联,然后在溶液中用碘进行传统氧化。由于使用了 RAM,这两种方法都成功地放大到了数克的量级,为更大规模的放大提供了可能,可连续放大到数百公斤。
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