| Literature DB >> 35796984 |
Michael Pilsl1, Florian B Heiss1, Gisela Pöll1, Mona Höcherl1, Philipp Milkereit1, Christoph Engel2.
Abstract
Recent technological progress revealed new prospects of high-resolution structure determination of macromolecular complexes using cryo-electron microscopy (cryo-EM) . In the field of RNA polymerase (Pol) I research, a number of cryo-EM studies contributed to understanding the highly specialized mechanisms underlying the transcription of ribosomal RNA genes . Despite a broad applicability of the cryo-EM method itself, preparation of samples for high-resolution data collection can be challenging. Here, we describe strategies for the purification and stabilization of Pol I complexes, exemplarily considering advantages and disadvantages of the methodology. We further provide an easy-to-implement protocol for the coating of EM-grids with self-made carbon support films. In sum, we present an efficient workflow for cryo-grid preparation and optimization, including early stage cryo-EM screening that can be adapted to a wide range of soluble samples for high-resolution structure determination .Entities:
Keywords: Grid preparation; Negative staining; Plunge freezing; Preparation of transcription complexes; RNA polymerase I; Single-particle cryo-electron microscopy
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Year: 2022 PMID: 35796984 DOI: 10.1007/978-1-0716-2501-9_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745