Schäffner A R, Jorgensen E D, McAllister W T, Hartmann G R
Institut für Biochemie, Ludwig-Maximilians-Universität, München, FRG.
Nucleic Acids Res. 1987 Nov 11;15(21):8773-81. doi: 10.1093/nar/15.21.8773.
We describe a method for specifically labelling T7 RNA polymerase at (or near) the active site. Enzyme molecules that have been modified by covalent attachment of a benzaldehyde nucleotide derivative in the presence of template DNA are subsequently incubated with radioactively labelled nucleoside triphosphates. Labelling of the enzyme occurs as a result of the formation of the first phosphodiester bond. The labelling is template-directed and the expected specificity of initiation at individual T7 promoters is observed. The label has been localized to an 80 kd tryptic fragment that contains the carboxy-terminal portion of the enzyme.
我们描述了一种在活性位点(或其附近)特异性标记T7 RNA聚合酶的方法。在模板DNA存在的情况下,通过共价连接苯甲醛核苷酸衍生物而被修饰的酶分子,随后与放射性标记的核苷三磷酸一起孵育。酶的标记是由于第一个磷酸二酯键的形成而发生的。这种标记是模板导向的,并且观察到了在各个T7启动子处起始的预期特异性。该标记已定位到一个80 kd的胰蛋白酶片段,该片段包含酶的羧基末端部分。