A versatile oblique plane microscope for large-scale and high-resolution imaging of subcellular dynamics

Etai Sapoznik(The University of Texas Southwestern Medical Center), Bo-Jui Chang(The University of Texas Southwestern Medical Center), Jaewon Huh(The University of Texas Southwestern Medical Center), Robert J. Ju(The University of Queensland), Evgenia V Azarova(The University of Texas Southwestern Medical Center), Theresa Pohlkamp(The University of Texas Southwestern Medical Center), Erik S. Welf(The University of Texas Southwestern Medical Center), David Broadbent(Michigan State University), Alexandre F. Carisey(Baylor College of Medicine), Samantha J. Stehbens(The University of Queensland), Kyung Min Lee(The University of Texas Southwestern Medical Center), Arnaldo Marín(University of Chile), Ariella B. Hanker(The University of Texas Southwestern Medical Center), Jens C. Schmidt(Michigan State University), Carlos L. Arteaga(The University of Texas Southwestern Medical Center), Bin Yang(Chan Zuckerberg Initiative (United States)), Yoshihiko Kobayashi(Duke University), Purushothama Rao Tata(Duke University), Rory Kruithoff(Arizona State University), Konstantin Doubrovinski(The University of Texas Southwestern Medical Center), Douglas P. Shepherd(Arizona State University), Alfred Millett-Sikking, Andrew G. York, Kevin M. Dean(The University of Texas Southwestern Medical Center), Reto Fiolka(The University of Texas Southwestern Medical Center)
eLife
November 12, 2020
Cited by 205Open Access
Full Text

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.


Related Papers

No related papers found

Powered by citation graph analysis