Making plant tissue accessible for cryo-electron tomography

作者：Matthias Pöge, Marcel Dickmanns, Peng Xu, Meijing Li, Oda Helene Schiøtz, Christoph J. O. Kaiser, Jun Ma, Anna Bieber, Cristina Capitanio, Johann Brenner, Margot Riggi, Sven Klumpe, Manuel Miras, Neda S. Kazemein Jasemi, Waltraud X. Schulze, Rüdiger Simon, Wolf B Frommer, Jürgen M. Plitzko, Wolfgang Baumeister · 发表于：eLife · 年份：2025 · DOI：10.7554/elife.106455.1 · 被引用次数：6 · 研究领域：Advanced Electron Microscopy Techniques and Applications、Characterization and Applications of Magnetic Nanoparticles、Electron and X-Ray Spectroscopy Techniques

Abstract Cryo-Electron Tomography (cryo-ET) allows to visualize the molecular architecture of pristinely preserved cells and tissues. The workflow of sample preparation for cryo-ET is rather complex; it involves vitrification by rapid freezing followed by cryo-Focused Ion Beam (FIB) milling rendering the volumes of interest thin enough for cryo-ET data acquisition. The established protocols for single cells grown on or deposited on EM-grids are not suitable for multicellular plant tissues. Plunge-freezing does not yield vitrified samples in most cases and must be replaced by high-pressure freezing. This, in turn, necessitates extensive modifications of the subsequent FIB milling procedures. In this communication we describe procedures for sample screening, targeted FIB milling guided by cryo-fluorescence microscopy and a novel lamella trimming step that allows to obtain homogenously thin lamellae suitable for cryo-ET. We have tested all the steps along the workflow with a variety of plant tissues including the moss Physcomitrium patens and tissues of Arabidopsis thaliana and Limonium bicolor. We could demonstrate that the workflow optimized for plant tissues allows to attain subnanometer resolution in cases where subtomogram averaging is applicable.