Wyatt J R, Chastain M, Puglisi J D
University of California, Berkeley.
Biotechniques. 1991 Dec;11(6):764-9.
Biophysical studies of RNA oligonucleotides require milligram amounts of RNA of specific length and sequence. Transcription from synthetic DNA templates using T7 RNA polymerase is a convenient method for synthesis of RNA oligonucleotides ranging in size from 9 to about 45 nucleotides. Here we present methods that make the large-scale synthesis of RNA oligonucleotides practical. This paper describes a rapid method for isolating T7 RNA polymerase free from RNases for use in transcription reactions. Protocols are also described for purification of the desired RNA oligonucleotide from the other products of transcription.
对RNA寡核苷酸进行生物物理研究需要毫克级特定长度和序列的RNA。使用T7 RNA聚合酶从合成DNA模板进行转录是合成大小从9到约45个核苷酸不等的RNA寡核苷酸的便捷方法。在此,我们介绍了使RNA寡核苷酸大规模合成切实可行的方法。本文描述了一种快速方法,用于分离不含核糖核酸酶的T7 RNA聚合酶以用于转录反应。还介绍了从转录的其他产物中纯化所需RNA寡核苷酸的方案。