Lattice light sheet microscopy: imaging molecules, cells, and embryos at high spatiotemporal resolution
Wesley Legant a
a HHMI, 19700 Helix Drive, Ashburn, 20147, United States
Proceedings of New Advances in Probing Cell-ECM Interactions (CellMatrix)
Berlin, Germany, 2016 October 20th - 21st
Organizers: Ovijit Chaudhuri, Allen Liu and Sapun Parekh
Oral, Wesley Legant, presentation 006
Publication date: 25th July 2016

     By definition, living specimens are animate.  Therefore, a full understanding of dynamic biological systems will only be obtained by observing them with enough 4D spatio-temporal resolution and for a sufficient duration, to capture the phenomena of interest.  Unfortunately, conventional widefield or confocal microscopes are either too slow, lack the spatial resolution, or induce too much photodamage to meet these requirements.  To address these limitations, we have developed Lattice Light Sheet Microscopy, a new sub-cellular light-sheet microscopy method capable of imaging fast 3D dynamic processes in vivo at signal to noise levels approaching those obtained by total internal reflection fluorescence (TIRF) illumination.  By utilizing 2D optical lattices, we generate a thin (~800 nm full width half maximum) plane of light coincident with the focus of a high numerical aperture detection objective.  Using this technique, we demonstrate substantial advantages in speed, sensitivity and reduced phototoxicity compared to conventional point scanning and spinning disc confocal microscopes as well as light-sheet microscopes utilizing single Gaussian or Bessel beams.  We leverage these advantages to image samples ranging over three orders of magnitude in length scale from single molecules to whole embryos.  Specific examples include: single molecule tracking of fluorescently tagged transcription factors in densely labeled embryonic stem cell spheroids, 3D imaging of microtubule growth phases and organelle dynamics throughout the course of cell division, 3D cell migration through collagen matrices, and protein localization throughout the course of dorsal closure in Drosophila embryos.  Further, by combining lattice light sheet microscopy with point accumulation for imaging of nanoscale topography (PAINT) microscopy and novel fluorescent probes, we demonstrate 3D super-resolution localization microscopy over large fields of view and in thick 3D samples such as dividing cells and small embryos.



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