Your browser doesn't support javascript.
loading
FAST-EM array tomography: a workflow for multibeam volume electron microscopy.
Kievits, Arent J; Duinkerken, B H Peter; Lane, Ryan; de Heus, Cecilia; van Beijeren Bergen En Henegouwen, Daan; Höppener, Tibbe; Wolters, Anouk H G; Liv, Nalan; Giepmans, Ben N G; Hoogenboom, Jacob P.
Afiliação
  • Kievits AJ; Department of Imaging Physics, Delft University of Technology, Delft, The Netherlands.
  • Duinkerken BHP; Department of Biomedical Sciences, University Medical Center Groningen, Groningen, The Netherlands.
  • Lane R; Department of Imaging Physics, Delft University of Technology, Delft, The Netherlands.
  • de Heus C; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
  • van Beijeren Bergen En Henegouwen D; Department of Biomedical Sciences, University Medical Center Groningen, Groningen, The Netherlands.
  • Höppener T; Department of Imaging Physics, Delft University of Technology, Delft, The Netherlands.
  • Wolters AHG; Department of Biomedical Sciences, University Medical Center Groningen, Groningen, The Netherlands.
  • Liv N; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Giepmans BNG; Department of Biomedical Sciences, University Medical Center Groningen, Groningen, The Netherlands.
  • Hoogenboom JP; Department of Imaging Physics, Delft University of Technology, Delft, The Netherlands.
Methods Microsc ; 1(1): 49-64, 2024 Apr.
Article em En | MEDLINE | ID: mdl-39119255
ABSTRACT
Elucidating the 3D nanoscale structure of tissues and cells is essential for understanding the complexity of biological processes. Electron microscopy (EM) offers the resolution needed for reliable interpretation, but the limited throughput of electron microscopes has hindered its ability to effectively image large volumes. We report a workflow for volume EM with FAST-EM, a novel multibeam scanning transmission electron microscope that speeds up acquisition by scanning the sample in parallel with 64 electron beams. FAST-EM makes use of optical detection to separate the signals of the individual beams. The acquisition and 3D reconstruction of ultrastructural data from multiple biological samples is demonstrated. The results show that the workflow is capable of producing large reconstructed volumes with high resolution and contrast to address biological research questions within feasible acquisition time frames.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article