| Literature DB >> 33179596 |
Etai Sapoznik1,2, Bo-Jui Chang1, Jaewon Huh1,2, Robert J Ju3, Evgenia V Azarova1, Theresa Pohlkamp4, Erik S Welf1,2, David Broadbent5, Alexandre F Carisey6, Samantha J Stehbens3, Kyung-Min Lee7, Arnaldo Marín7,8, Ariella B Hanker7, Jens C Schmidt5,9, Carlos L Arteaga7, Bin Yang10, Yoshihiko Kobayashi11, Purushothama Rao Tata11, Rory Kruithoff12, Konstantin Doubrovinski1,13, Douglas P Shepherd12, Alfred Millett-Sikking14, Andrew G York14, Kevin M Dean1, Reto P Fiolka1,2.
Abstract
We present an oblique plane microscope (OPM) that uses a bespoke glass-tipped tertiary objective to improve the resolution, field of view, and usability over previous variants. Owing to its high numerical aperture optics, this microscope achieves lateral and axial resolutions that are comparable to the square illumination mode of lattice light-sheet microscopy, but in a user friendly and versatile format. Given this performance, we demonstrate high-resolution imaging of clathrin-mediated endocytosis, vimentin, the endoplasmic reticulum, membrane dynamics, and Natural Killer-mediated cytotoxicity. Furthermore, we image biological phenomena that would be otherwise challenging or impossible to perform in a traditional light-sheet microscope geometry, including cell migration through confined spaces within a microfluidic device, subcellular photoactivation of Rac1, diffusion of cytoplasmic rheological tracers at a volumetric rate of 14 Hz, and large field of view imaging of neurons, developing embryos, and centimeter-scale tissue sections.Entities:
Keywords: cell biology; fluorescence; light-sheet; microfluidics; microscopy; none; optogenetics; particle tracking
Mesh:
Year: 2020 PMID: 33179596 PMCID: PMC7707824 DOI: 10.7554/eLife.57681
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140