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Cryo-Structured Illumination Microscopic Data Collection from Cryogenically Preserved Cells.
Vyas, Nina; Perry, Nina; Okolo, Chidinma A; Kounatidis, Ilias; Fish, Thomas M; Nahas, Kamal L; Jadhav, Archana; Koronfel, Mohamed A; Groen, Johannes; Pereiro, Eva; Dobbie, Ian M; Harkiolaki, Maria.
Afiliación
  • Vyas N; Harwell Science and Innovation Campus, Beamline B24, Diamond Light Source; nina.vyas@diamond.ac.uk.
  • Perry N; Harwell Science and Innovation Campus, Beamline B24, Diamond Light Source.
  • Okolo CA; Harwell Science and Innovation Campus, Beamline B24, Diamond Light Source.
  • Kounatidis I; Harwell Science and Innovation Campus, Beamline B24, Diamond Light Source.
  • Fish TM; Harwell Science and Innovation Campus, Beamline B24, Diamond Light Source.
  • Nahas KL; Harwell Science and Innovation Campus, Beamline B24, Diamond Light Source; Division of Virology, Department of Pathology, University of Cambridge.
  • Jadhav A; Harwell Science and Innovation Campus, Beamline B24, Diamond Light Source.
  • Koronfel MA; Harwell Science and Innovation Campus, Beamline B24, Diamond Light Source.
  • Groen J; ALBA Synchrotron, Beamline 09 - MISTRAL.
  • Pereiro E; ALBA Synchrotron, Beamline 09 - MISTRAL.
  • Dobbie IM; Micron Advanced Imaging Consortium, Department of Biochemistry, University of Oxford; ian.dobbie@bioch.ox.ac.uk.
  • Harkiolaki M; Harwell Science and Innovation Campus, Beamline B24, Diamond Light Source; maria.harkiolaki@diamond.ac.uk.
J Vis Exp ; (171)2021 05 28.
Article en En | MEDLINE | ID: mdl-34125093
Three-dimensional (3D) structured illumination microscopy (SIM) allows imaging of fluorescently labelled cellular structures at higher resolution than conventional fluorescence microscopy. This super-resolution (SR) technique enables visualization of molecular processes in whole cells and has the potential to be used in conjunction with electron microscopy and X-ray tomography to correlate structural and functional information. A SIM microscope for cryogenically preserved samples (cryoSIM) has recently been commissioned at the correlative cryo-imaging beamline B24 at the UK synchrotron. It was designed specifically for 3D imaging of biological samples at cryogenic temperatures in a manner compatible with subsequent imaging of the same samples by X-ray microscopy methods such as cryo-soft X-ray tomography. This video article provides detailed methods and protocols for successful imaging using the cryoSIM. In addition to instructions on the operation of the cryoSIM microscope, recommendations have been included regarding the choice of samples, fluorophores, and parameter settings. The protocol is demonstrated in U2OS cell samples whose mitochondria and tubulin have been fluorescently labelled.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Criopreservación / Técnicas Citológicas / Colorantes Fluorescentes Límite: Humans Idioma: En Revista: J Vis Exp Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Criopreservación / Técnicas Citológicas / Colorantes Fluorescentes Límite: Humans Idioma: En Revista: J Vis Exp Año: 2021 Tipo del documento: Article
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