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Real-time multi-angle projection imaging of biological dynamics.
Chang, Bo-Jui; Manton, James D; Sapoznik, Etai; Pohlkamp, Theresa; Terrones, Tamara S; Welf, Erik S; Murali, Vasanth S; Roudot, Philippe; Hake, Kayley; Whitehead, Lachlan; York, Andrew G; Dean, Kevin M; Fiolka, Reto.
Affiliation
  • Chang BJ; Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Manton JD; MRC Laboratory of Molecular Biology, Cambridge, UK.
  • Sapoznik E; Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Pohlkamp T; Department of Molecular Genetics, UT Southwestern Medical Center, Dallas, TX, USA.
  • Terrones TS; Department of Molecular Genetics, UT Southwestern Medical Center, Dallas, TX, USA.
  • Welf ES; Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Murali VS; Lyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Roudot P; Department of Cell Biology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Hake K; Lyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • Whitehead L; Lyda Hill Department of Bioinformatics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
  • York AG; Calico Life Sciences LLC, South San Francisco, CA, USA.
  • Dean KM; Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.
  • Fiolka R; Department of Medical Biology, University of Melbourne, Parkville, Victoria, Australia.
Nat Methods ; 18(7): 829-834, 2021 07.
Article in En | MEDLINE | ID: mdl-34183831
ABSTRACT
We introduce a cost-effective and easily implementable scan unit that converts any camera-based microscope with optical sectioning capability into a multi-angle projection imaging system. Projection imaging reduces data overhead and accelerates imaging by a factor of >100, while also allowing users to readily view biological phenomena of interest from multiple perspectives on the fly. By rapidly interrogating the sample from just two perspectives, our method also enables real-time stereoscopic imaging and three-dimensional particle localization. We demonstrate projection imaging with spinning disk confocal, lattice light-sheet, multidirectional illumination light-sheet and oblique plane microscopes on specimens that range from organelles in single cells to the vasculature of a zebrafish embryo. Furthermore, we leverage our projection method to rapidly image cancer cell morphodynamics and calcium signaling in cultured neurons at rates up to 119 Hz as well as to simultaneously image orthogonal views of a beating embryonic zebrafish heart.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Image Processing, Computer-Assisted / Microscopy, Confocal Limits: Animals / Female / Humans / Male Language: En Journal: Nat Methods Journal subject: TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2021 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Image Processing, Computer-Assisted / Microscopy, Confocal Limits: Animals / Female / Humans / Male Language: En Journal: Nat Methods Journal subject: TECNICAS E PROCEDIMENTOS DE LABORATORIO Year: 2021 Type: Article Affiliation country: United States