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Isotropic imaging across spatial scales with axially swept light-sheet microscopy.
Dean, Kevin M; Chakraborty, Tonmoy; Daetwyler, Stephan; Lin, Jinlong; Garrelts, Gerard; M'Saad, Ons; Mekbib, Hannahmariam T; Voigt, Fabian F; Schaettin, Martina; Stoeckli, Esther T; Helmchen, Fritjof; Bewersdorf, Joerg; Fiolka, Reto.
Afiliación
  • Dean KM; Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA. kevin.dean@utsouthwestern.edu.
  • Chakraborty T; Lyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA. kevin.dean@utsouthwestern.edu.
  • Daetwyler S; Department of Physics and Astronomy, University of New Mexico, Albuquerque, NM, USA.
  • Lin J; Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Garrelts G; Lyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • M'Saad O; Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Mekbib HT; Lyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Voigt FF; Coleman Technologies, Inc. D.B.A., Sciotex, Newtown Square, PA, USA.
  • Schaettin M; Department of Cell Biology, Yale University, New Haven, CT, USA.
  • Stoeckli ET; Department of Biomedical Engineering, Yale University, New Haven, CT, USA.
  • Helmchen F; Department of Cell Biology, Yale University, New Haven, CT, USA.
  • Bewersdorf J; Department of Biomedical Engineering, Yale University, New Haven, CT, USA.
  • Fiolka R; Neuroscience Center Zurich, Zurich, Switzerland.
Nat Protoc ; 17(9): 2025-2053, 2022 09.
Article en En | MEDLINE | ID: mdl-35831614
ABSTRACT
Light-sheet fluorescence microscopy is a rapidly growing technique that has gained tremendous popularity in the life sciences owing to its high-spatiotemporal resolution and gentle, non-phototoxic illumination. In this protocol, we provide detailed directions for the assembly and operation of a versatile light-sheet fluorescence microscopy variant, referred to as axially swept light-sheet microscopy (ASLM), that delivers an unparalleled combination of field of view, optical resolution and optical sectioning. To democratize ASLM, we provide an overview of its working principle and applications to biological imaging, as well as pragmatic tips for the assembly, alignment and control of its optical systems. Furthermore, we provide detailed part lists and schematics for several variants of ASLM that together can resolve molecular detail in chemically expanded samples, subcellular organization in living cells or the anatomical composition of chemically cleared intact organisms. We also provide software for instrument control and discuss how users can tune imaging parameters to accommodate diverse sample types. Thus, this protocol will serve not only as a guide for both introductory and advanced users adopting ASLM, but as a useful resource for any individual interested in deploying custom imaging technology. We expect that building an ASLM will take ~1-2 months, depending on the experience of the instrument builder and the version of the instrument.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Programas Informáticos / Imagenología Tridimensional Idioma: En Revista: Nat Protoc Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Programas Informáticos / Imagenología Tridimensional Idioma: En Revista: Nat Protoc Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos
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