Hobbs F W, Yarem J A
Dupont Merck Pharmaceutical Company, Wilmington, DE 19880.
Biotechniques. 1993 Apr;14(4):584-91.
Purification of oligonucleotides by HPLC is limited by association between failure sequences and full-length oligonucleotide. We describe a protocol for denaturing purification of 5'-dimethoxytritylated oligonucleotides that ensures that separation of tritylated and non-tritylated species will not be complicated by strand association. Fully denaturing conditions are produced by the use of tetraethylammonium hydroxide, which is a basic reagent with ion-pairing properties similar to triethylammonium acetate. The method also includes two other convenient features: a) the option of loading the crude oligonucleotide without removing concentrated ammonium hydroxide and b) detritylation on the column with separation of dimethoxytrityl alcohol.
通过高效液相色谱法(HPLC)纯化寡核苷酸受到失败序列与全长寡核苷酸之间缔合的限制。我们描述了一种用于5'-二甲氧基三苯甲基化寡核苷酸变性纯化的方案,该方案可确保三苯甲基化和非三苯甲基化物种的分离不会因链缔合而变得复杂。使用氢氧化四乙铵可产生完全变性的条件,氢氧化四乙铵是一种具有与乙酸三乙铵类似的离子配对特性的碱性试剂。该方法还包括另外两个便利之处:a)无需去除浓氢氧化铵即可加载粗寡核苷酸的选项;b)在柱上进行脱三苯甲基化并分离二甲氧基三苯甲醇。