Research Group CryoEM Technology, Max Planck Institute of Biochemistry, Martinsried, Germany.
Department of Cell and Virus Structure, Max Planck Institute of Biochemistry, Martinsried, Germany.
Nat Methods. 2024 Sep;21(9):1684-1692. doi: 10.1038/s41592-023-02113-5. Epub 2023 Dec 18.
Cryo-focused ion beam milling of frozen-hydrated cells and subsequent cryo-electron tomography (cryo-ET) has enabled the structural elucidation of macromolecular complexes directly inside cells. Application of the technique to multicellular organisms and tissues, however, is still limited by sample preparation. While high-pressure freezing enables the vitrification of thicker samples, it prolongs subsequent preparation due to increased thinning times and the need for extraction procedures. Additionally, thinning removes large portions of the specimen, restricting the imageable volume to the thickness of the final lamella, typically <300 nm. Here we introduce Serial Lift-Out, an enhanced lift-out technique that increases throughput and obtainable contextual information by preparing multiple sections from single transfers. We apply Serial Lift-Out to Caenorhabditis elegans L1 larvae, yielding a cryo-ET dataset sampling the worm's anterior-posterior axis, and resolve its ribosome structure to 7 Å and a subregion of the 11-protofilament microtubule to 13 Å, illustrating how Serial Lift-Out enables the study of multicellular molecular anatomy.
冷冻聚焦离子束铣削和随后的冷冻电子断层扫描(cryo-ET)使我们能够直接在细胞内解析大分子复合物的结构。然而,该技术在多细胞生物和组织中的应用仍然受到样品制备的限制。虽然高压冷冻能够使较厚的样品玻璃化,但由于增加了变薄时间和需要提取程序,后续的准备工作会延长。此外,变薄会去除大部分样本,将可成像的体积限制在最终薄片的厚度内,通常<300nm。在这里,我们引入了 Serial Lift-Out,这是一种增强型的提取技术,通过从单个转移物中制备多个切片来提高通量和可获得的上下文信息。我们将 Serial Lift-Out 应用于秀丽隐杆线虫 L1 幼虫,获得了一个采样线虫前后轴的 cryo-ET 数据集,并将其核糖体结构解析到 7Å 和 11 原丝微管的一个亚区到 13Å,说明了 Serial Lift-Out 如何能够用于研究多细胞分子解剖结构。