4.8 Article

3D Correlative Cryo-Structured Illumination Fluorescence and Soft X-ray Microscopy Elucidates Reovirus Intracellular Release Pathway

期刊

CELL
卷 182, 期 2, 页码 515-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2020.05.051

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资金

  1. Infectious Diseases Imaging Platform (IDIP) at the Center for Integrative Infectious Disease Research, Heidelberg, Germany
  2. Wellcome Centre for Human Genetics by the Wellcome Trust ISSF [105605/Z/14/Z]
  3. Wellcome Trust [203141/Z/16/Z]
  4. Wellcome Strategic Awards [091911, 107457]
  5. ANR [ANR-18-CE45-0015, ANR-10-INBS-04]
  6. Wellcome Investigator Award [200835/Z/16/Z]
  7. Heisenberg [BO 4340/1-1, SFB1129]
  8. Deutsche Forschungsgemeinschaft (DFG) [240245660, SFB 1129]
  9. Brigitte-Schlieben Lange Program from the state of Baden Wurttemberg, Germany
  10. DFG [416072091]
  11. Diamond
  12. MRC [MR/N00065X/1]
  13. Diamond Light Source [MX21046, MX18314]
  14. Agence Nationale de la Recherche (ANR) [ANR-18-CE45-0015] Funding Source: Agence Nationale de la Recherche (ANR)
  15. MRC [MR/N00065X/1, MR/K01577X/1] Funding Source: UKRI
  16. Wellcome Trust [105605/Z/14/Z] Funding Source: Wellcome Trust

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Imaging of biological matter across resolution scales entails the challenge of preserving the direct and unambiguous correlation of subject features from the macroscopic to the microscopic level, Here, we present a correlative imaging platform developed specifically for imaging cells in 3D under cryogenic conditions by using X-rays and visible light. Rapid cryo-preservation of biological specimens is the current gold standard in sample preparation for ultrastructural analysis in X-ray imaging. However, cryogenic fluorescence localization methods are, in their majority, diffraction-limited and fail to deliver matching resolution, We addressed this technological gap by developing an integrated, user-friendly platform for 3D correlative imaging of cells in vitreous ice by using super-resolution structured illumination microscopy in conjunction with soft X-ray tomography. The power of this approach is demonstrated by studying the process of reovirus release from intracellular vesicles during the early stages of infection and identifying intracellular virus-induced structures.

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