Wincott F E
Ribozyme Pharmaceuticals, Inc., Boulder, Colorado, USA.
Curr Protoc Nucleic Acid Chem. 2001 May;Chapter 3:Unit 3.5. doi: 10.1002/0471142700.nc0305s00.
Advances in oligoribonucleotide synthesis have lagged behind those in oligodeoxyribonucleotide synthesis because of the difficulty in identifying orthogonal protecting groups for the 2'- and 5'-hydroxyls. Adaptation of the phosphoramidite method for DNA synthesis to RNA synthesis has greatly improved our understanding of RNA. It allows site-specific introduction of modified nucleosides to any position in an RNA molecule, as well as introduction of variations at multiple sites in the molecule. This overview discusses issues that are relevant to RNA synthesis by the phosphoramidite approach, including supports used, activation of the ribonucleoside phosphoramidites, and protection of the nucleobase, phosphate, and 2'- and 5'-hydroxyls.
由于难以确定2'-和5'-羟基的正交保护基团,寡核糖核苷酸合成的进展落后于寡脱氧核糖核苷酸合成。将用于DNA合成的亚磷酰胺方法应用于RNA合成,极大地增进了我们对RNA的理解。它允许将修饰的核苷位点特异性地引入RNA分子的任何位置,以及在分子的多个位点引入变异。本综述讨论了与通过亚磷酰胺方法进行RNA合成相关的问题,包括所用的载体、核糖核苷亚磷酰胺的活化以及碱基、磷酸基团和2'-和5'-羟基的保护。