Macdonald P M, Damha M J, Ganeshan K, Braich R, Zabarylo S V
Department of Chemistry, Erindale College, University of Toronto, Ontario M5S 1A2, Canada.
Nucleic Acids Res. 1996 Aug 1;24(15):2868-76. doi: 10.1093/nar/24.15.2868.
31P cross polarization (CP) magic angle spinning (MAS) nuclear magnetic resonance (NMR) spectra were acquired for various linear and branched di- and tri-nucleotides attached to a controlled pore glass (CPG) solid support. The technique readily distinguishes the oxidation state of the phosphorus atom (phosphate versus phosphate), the presence or absence of a protecting group attached directly to phosphorus (cyanoethyl), and other large changes in the phosphorus chemistry (phosphate versus phosphorothioate). However, differences in configurational details remote from the phosphorus atom, such as the attachment position of the ribose sugar (2'5' versus 3'5'), or the particulars of the nucleotide bases (adenine versus uridine versus thymine), could not be resolved. When different stages of the oligonucleotide synthetic cycle were examined, 31P CPMAS NMR revealed that the cyanoethyl protecting group is removed during the course of chain assembly.
对连接到可控孔径玻璃(CPG)固体支持物上的各种线性和支化二核苷酸及三核苷酸进行了31P交叉极化(CP)魔角旋转(MAS)核磁共振(NMR)光谱测定。该技术能够轻松区分磷原子的氧化态(磷酸根与磷酸)、直接连接到磷上的保护基团(氰乙基)的存在与否以及磷化学的其他重大变化(磷酸根与硫代磷酸根)。然而,远离磷原子的构型细节差异,如核糖糖的连接位置(2'5'与3'5')或核苷酸碱基的具体情况(腺嘌呤与尿嘧啶与胸腺嘧啶),无法分辨。当检查寡核苷酸合成周期的不同阶段时,31P CPMAS NMR显示氰乙基保护基团在链组装过程中被去除。