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RNA化学合成的最新进展。

Recent advances in the chemical synthesis of RNA.

作者信息

Beaucage Serge L, Reese Colin B

机构信息

Food and Drug Administration, Bethesda, Maryland, USA.

出版信息

Curr Protoc Nucleic Acid Chem. 2009 Sep;Chapter 2:Unit 2.16 1-31. doi: 10.1002/0471142700.nc0216s38.

Abstract

As a consequence largely of recent developments in RNA interference (RNAi) research, the availability of rapid and efficient methods for the chemical synthesis of RNA sequences has become a matter of considerable urgency. This unit is concerned mainly with work that has been carried out, especially in the past decade, on the design of new and improved methods of RNA synthesis. The main criteria for the choice of protecting groups for the 2'-hydroxy functions of the ribonucleoside building blocks, which is arguably the most crucial strategic decision to be made, are discussed. A number of new ether-, acetal-, orthoester-, and ester-based 2'-protecting groups are described and their application, mainly in phosphoramidite-based solid-phase synthesis, is discussed in some detail. Brief consideration is also given to solution-phase RNA synthesis, which may well prove to be of great importance if a systemic drug is developed and multikilogram quantities of synthetic RNA sequences are required.

摘要

由于RNA干扰(RNAi)研究近期的发展,快速高效地化学合成RNA序列的方法变得极为迫切。本单元主要关注尤其是过去十年中在设计新的和改进的RNA合成方法方面所开展的工作。讨论了核糖核苷构建块2'-羟基功能保护基团选择的主要标准,这可以说是最关键的战略决策。描述了一些新的基于醚、缩醛、原酸酯和酯的2'-保护基团,并详细讨论了它们主要在基于亚磷酰胺的固相合成中的应用。还简要考虑了溶液相RNA合成,如果开发出一种全身药物并且需要数千克量的合成RNA序列,溶液相RNA合成很可能会被证明非常重要。

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