Padmapriya A A, Tang J, Agrawal S
Hybridon, Inc., Worcester, Massachusetts 01605.
Antisense Res Dev. 1994 Fall;4(3):185-99. doi: 10.1089/ard.1994.4.185.
Synthesis of oligonucleotides has been carried out on 1-, 2-, and 5-mmol scales using an appropriately modified automated, commercially available DNA synthesizer. The reaction cycles were optimized to obtain efficient coupling (> or = 97%). The synthesized oligonucleotide was purified by preparative reversed-phase liquid chromatography, followed by detritylation and desalting to obtain the oligonucleotides in the Na+ form. The purified oligonucleotides were characterized by 31P NMR, mass spectrometry, capillary gel electrophoresis, and ion-exchange high-performance liquid chromatography. By using these protocols, a 25-mer oligodeoxyribonucleotide can be synthesized on a 1-, 2-, or 5-mmole scale to obtain approximately 2.4, 4.8, or 12 g of purified product.
使用经过适当改装的市售自动化DNA合成仪,已在1毫摩尔、2毫摩尔和5毫摩尔规模上进行了寡核苷酸的合成。对反应循环进行了优化,以获得高效偶联(≥97%)。合成的寡核苷酸通过制备型反相液相色谱进行纯化,随后进行脱三苯甲基化和脱盐,以获得Na⁺形式的寡核苷酸。纯化的寡核苷酸通过³¹P NMR、质谱、毛细管凝胶电泳和离子交换高效液相色谱进行表征。通过使用这些方案,可以在1毫摩尔、2毫摩尔或5毫摩尔规模上合成25聚体寡脱氧核糖核苷酸,以获得约2.4克、4.8克或12克的纯化产物。