Chi Y Y, Bassel A R
J Virol. 1974 Jun;13(6):1194-9. doi: 10.1128/JVI.13.6.1194-1199.1974.
A method for preparation of single-stranded RNA for electron microscopy determination of molecular weight is reported. The method uses treatment with formaldehyde at elevated temperatures to remove secondary structure and spreading in a protein monolayer from 50% formamide onto a 50% formamide hypophase. Molecular weights were determined for some bacterial and animal viruses, for which conflicting values had been reported earlier. Molecular weights determined by the method, using Escherichia coli large subunit rRNA for a standard (1.1 x 10(6)), are as follows: E. coli small subunit rRNA, 0.53 x 10(6); coliphage f2-RNA, 1.3 x 10(6); Qbeta-RNA, 1.55 x 10(6); and Newcastle disease virus RNA, 5.78 x 10(6).
报道了一种用于制备单链RNA以通过电子显微镜测定分子量的方法。该方法采用在高温下用甲醛处理以去除二级结构,并在从50%甲酰胺到50%甲酰胺亚相的蛋白质单层中铺展。测定了一些细菌和动物病毒的分子量,此前曾报道过这些病毒分子量存在相互矛盾的值。使用大肠杆菌大亚基rRNA作为标准(1.1×10⁶),通过该方法测定的分子量如下:大肠杆菌小亚基rRNA,0.53×10⁶;大肠杆菌噬菌体f2-RNA,1.3×10⁶;Qβ-RNA,1.55×10⁶;以及新城疫病毒RNA,5.78×10⁶。