Flexible Multi-Beam Light-Sheet Fluorescence Microscope for Live Imaging Without Striping Artifacts
Authors: Sancataldo G., Gavryusev V., de Vito G., Turrini L., Locatelli M., Fornetto C., Tiso N., Vanzi F., Silvestri L., Pavone FS.
Autors Affiliation: Univ Florence, Dept Phys & Astron, Sesto Fiorentino, Italy; Univ Florence, European Lab Nonlinear Spect, Sesto Fiorentino, Italy; CNR, Natl Inst Opt, Sesto Fiorentino, Italy; Univ Padua, Dept Biol, Padua, Italy; Univ Florence, Dept Biol, Sesto Fiorentino, Italy
Abstract: The development of light-sheet fluorescence microscopy (LSFM) has greatly expanded the experimental capabilities in many biological and biomedical research fields, enabling for example live studies of murine and zebra fish neural activity or of cell growth and division. The key feature of the method is the selective illumination of a sample single plane, providing an intrinsic optical sectioning and allowing direct 2D image recording. On the other hand, this excitation scheme is more affected by absorption or scattering artifacts in comparison to point scanning methods, leading to un-even illumination. We present here an easily implementable method, based on acousto-optical deflectors (AOD), to overcome this obstacle. We report the advantages provided by flexible and fast AODs in generating simultaneous angled multiple beams from a single laser beam and in fast light sheet pivoting and we demonstrate the suppression of illumination artifacts.
Journal/Review: FRONTIERS IN NEUROANATOMY
Volume: 13 Pages from: 7-1 to: 7-8
KeyWords: light-sheet fluorescence microscopy; striping artifacts; fast volumetric imaging; acousto optic deflector; brain imaging; zebrafishDOI: 10.3389/fnana.2019.00007Citations: 2data from “WEB OF SCIENCE” (of Thomson Reuters) are update at: 2020-06-28References taken from IsiWeb of Knowledge: (subscribers only)Connecting to view paper tab on IsiWeb: Click hereConnecting to view citations from IsiWeb: Click here