Szer W, Leffler S
Proc Natl Acad Sci U S A. 1974 Sep;71(9):3611-5. doi: 10.1073/pnas.71.9.3611.
MS2 RNA binds at 0 degrees to 30S subunits from E. coli and, to a smaller extent, to those of a Pseudomonas species, as judged by filtration on nitrocellulose membranes; this mRNA does not bind to 30S subunits from Bacillus brevis or Caulobacter crescentus. Binding does not depend on the presence of initiation factors; it is sensitive to aurintricarboxylic acid but insensitive to edeine and is competitive with such synthetic polynucleotides as poly(U) and poly(AUG). Complex formation can also be detected by electrophoresis on polyacrylamide-agarose gels. By this procedure, E. coli 30S subunits are separated into two major components. Only the more slowly moving component, which contains the ribosomal protein S1, interacts with the RNA.
通过在硝酸纤维素膜上进行过滤判断,MS2 RNA在0摄氏度时与来自大肠杆菌的30S亚基结合,在较小程度上也与一种假单胞菌属物种的30S亚基结合;这种信使核糖核酸不与短短芽孢杆菌或新月柄杆菌的30S亚基结合。结合不依赖于起始因子的存在;它对金精三羧酸敏感,但对伊短菌素不敏感,并且与诸如聚(U)和聚(AUG)等合成多核苷酸具有竞争性。复合物的形成也可以通过在聚丙烯酰胺 - 琼脂糖凝胶上进行电泳来检测。通过这个程序,大肠杆菌30S亚基被分离成两个主要成分。只有移动较慢的成分,即含有核糖体蛋白S1的成分,与RNA相互作用。