Nelissen Frank H T, Heus Hans A, Wijmenga Sybren S
Biophysical Chemistry, Institute for Molecules and Materials, Radboud University, Heyendaalseweg 135, 6525AJ, Nijmegen, The Netherlands.
Methods Mol Biol. 2015;1316:33-44. doi: 10.1007/978-1-4939-2730-2_4.
Bacterial overproduction of recombinant RNA using a tRNA scaffold yields large amounts of chimeric RNA. For structural and functional characterizations of the RNA it is often necessary to remove the scaffold. Here we describe an efficient and facile method to release the RNA of interest from the tRNA scaffold by selective cleavage using cis-acting hammerhead ribozymes. After cleavage, the RNA of interest is purified to homogeneity using standard chromatographic and electrophoretic methods. Up to 5 mg of highly pure end-product RNA can be obtained from a single liter of bacterial culture.
利用tRNA支架进行细菌重组RNA的过量表达可产生大量嵌合RNA。为了对RNA进行结构和功能表征,通常需要去除支架。在此,我们描述了一种高效且简便的方法,即通过使用顺式作用锤头状核酶进行选择性切割,从tRNA支架上释放出感兴趣的RNA。切割后,使用标准的色谱和电泳方法将感兴趣的RNA纯化至同质。从一升细菌培养物中可获得高达5毫克的高纯度终产物RNA。