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Snapshot blotting: transfer of nucleic acids and nucleoprotein complexes from electrophoresis gels to grids for electron microscopy.

机译:快照印迹:将核酸和核蛋白复合物从电泳凝胶转移到电子显微镜的网格上。

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摘要

We present a technique, "snapshot blotting," for the electrophoretic transfer of nucleic acids and nucleoprotein complexes in gel electrophoresis bands onto highly stable carbon film-coated grids for imaging by electron microscopy. The method permits structural analysis of macromolecular species that have been resolved by a gel mobility-shift assay. To demonstrate the efficiency and integrity of the transfer process for a multiprotein-DNA assembly, we have imaged various species of a prokaryotic transcription complex, using the cleavage-defective EcoRI(Q111) protein as an orientation marker and as a blockade of transcription elongation. Snapshot blotting should be of great utility in the structural characterization of nucleic acids and protein-nucleic acid interactions.
机译:我们提出了一种“快照印迹”技术,用于将凝胶电泳带中的核酸和核蛋白复合物电泳转移到高度稳定的碳膜涂层网格上,以通过电子显微镜成像。该方法允许对已经通过凝胶迁移率移动分析法解决的大分子种类进行结构分析。为了证明多蛋白-DNA组装的转移过程的效率和完整性,我们使用裂解缺陷型EcoRI(Q111)蛋白作为方向标记和对转录伸长的阻断,对各种原核转录复合物进行了成像。快照印迹在核酸的结构表征和蛋白质-核酸相互作用中应具有很大的用途。

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