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Serial Lift-Out: sampling the molecular anatomy of whole organisms.
Schiøtz, Oda Helene; Kaiser, Christoph J O; Klumpe, Sven; Morado, Dustin R; Poege, Matthias; Schneider, Jonathan; Beck, Florian; Klebl, David P; Thompson, Christopher; Plitzko, Jürgen M.
Affiliation
  • Schiøtz OH; Research Group CryoEM Technology, Max Planck Institute of Biochemistry, Martinsried, Germany.
  • Kaiser CJO; Research Group CryoEM Technology, Max Planck Institute of Biochemistry, Martinsried, Germany.
  • Klumpe S; Research Group CryoEM Technology, Max Planck Institute of Biochemistry, Martinsried, Germany. klumpe@biochem.mpg.de.
  • Morado DR; Department of Cell and Virus Structure, Max Planck Institute of Biochemistry, Martinsried, Germany.
  • Poege M; Department for Biochemistry and Biophysics, Science for Life Laboratory, Stockholm University, Stockholm, Sweden.
  • Schneider J; Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, Martinsried, Germany.
  • Beck F; Department of Molecular Structural Biology, Max Planck Institute of Biochemistry, Martinsried, Germany.
  • Klebl DP; Research Group CryoEM Technology, Max Planck Institute of Biochemistry, Martinsried, Germany.
  • Thompson C; Department of Cell and Virus Structure, Max Planck Institute of Biochemistry, Martinsried, Germany.
  • Plitzko JM; Materials and Structural Analysis, Thermo Fisher Scientific, Eindhoven, the Netherlands.
Nat Methods ; 21(9): 1684-1692, 2024 Sep.
Article in En | MEDLINE | ID: mdl-38110637
ABSTRACT
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.
Subject(s)

Full text: 1 Database: MEDLINE Main subject: Caenorhabditis elegans / Cryoelectron Microscopy / Electron Microscope Tomography Limits: Animals Language: En Journal: Nat Methods / Nat. methods / Nature methods Journal subject: TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2024 Type: Article Affiliation country: Germany

Full text: 1 Database: MEDLINE Main subject: Caenorhabditis elegans / Cryoelectron Microscopy / Electron Microscope Tomography Limits: Animals Language: En Journal: Nat Methods / Nat. methods / Nature methods Journal subject: TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2024 Type: Article Affiliation country: Germany