Broker T R, Angerer L M, Yen P H, Hershey N D, Davidson N
Nucleic Acids Res. 1978 Feb;5(2):363-84. doi: 10.1093/nar/5.2.363.
A method is described for indirect electron microscopic visualization and mapping of tRNA and other short transcripts hybridized to DNA. This method depends upon the attachment of the electron-dense protein ferritin to the RNA, the binding being mediated by the remarkably strong association of the egg white protein avidin with biotin. Biotin is covalently attached to the 3' end of tRNA using an NH2(CH2)5NH2 bridge. The tRNA-biotin adduct is hybridized to complementary DNA sequences present in a single stranded non-homology loop of a DNA:DNA heteroduplex. Avidin, covalently crosslinked to ferritin, is mixed with the heteroduplex and becomes bound to the hybridized tRNA-biotin. Observation of the DNA:RNA-biotin:avidin-ferritin complex by electron microscopy specifically and accurately reveals the position of the tRNA gene, with a frequency of labeling of approximately 50%.
本文描述了一种用于间接电子显微镜观察和定位与DNA杂交的tRNA及其他短转录本的方法。该方法依赖于将电子致密蛋白铁蛋白附着到RNA上,这种结合是由蛋清蛋白抗生物素蛋白与生物素之间非常强的结合作用介导的。使用NH2(CH2)5NH2桥将生物素共价连接到tRNA的3'末端。tRNA-生物素加合物与存在于DNA:DNA异源双链体单链非同源环中的互补DNA序列杂交。与铁蛋白共价交联的抗生物素蛋白与异源双链体混合,并与杂交的tRNA-生物素结合。通过电子显微镜观察DNA:RNA-生物素:抗生物素蛋白-铁蛋白复合物,可特异性且准确地揭示tRNA基因的位置,标记频率约为50%。