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Imaging of T7 RNA Polymerase Elongation Complexes by Atomic Force Microscopy

机译:T7 RNA聚合酶伸长复合物的原子力显微镜成像。

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摘要

Atomic force microscopy was used to visualize the complexes of bacteriophage T7 RNA polymerase (RNAP) with a DNA template during transcription. A 1414-bp fragment of linearized pGEMEX DNA was used as a template; the fragment contained the T7 promoter and terminator asymmetrically located at the template ends. Images of stable complexes of T7 RNAP and template terminal fragments were obtained for single molecules. Individual template DNA molecules bound with two or three T7 RNAP molecules, which corresponded to transcription initiation, elongation, and termination, and complexes containing RNA transcripts were imaged under conditions preventing nonspecific binding. The results suggest that T7 RNAP binds initially to the DNA template terminal fragment located near the promoter in order to exclude skipping the promoter site.
机译:原子力显微镜用于可视化转录过程中噬菌体T7 RNA聚合酶(RNAP)与DNA模板的复合物。线性化的pGEMEX DNA的1414bp片段用作模板;该片段含有不对称地位于模板末端的T7启动子和终止子。对于单个分子,获得了T7 RNAP和模板末端片段的稳定复合物的图像。与两个或三个T7 RNA分子结合的单个模板DNA分子,分别对应于转录的起始,延伸和终止,并在防止非特异性结合的条件下对含有RNA转录物的复合物进行成像。结果表明,T7 RNAP最初与位于启动子附近的DNA模板末端片段结合,以排除跳过启动子位点。

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