Expansion microscopy of C. elegans
Author(s)
Yu, Chih-Chieh Jay; Barry, Nicholas C; Wassie, Asmamaw T; Sinha, Anubhav; Bhattacharya, Abhishek; Asano, Shoh; Zhang, Chi; Chen, Fei; Hobert, Oliver; Goodman, Miriam B; Haspel, Gal; Boyden, Edward S; ... Show more Show less
DownloadPublished version (13.10Mb)
Publisher with Creative Commons License
Publisher with Creative Commons License
Creative Commons Attribution
Terms of use
Metadata
Show full item recordAbstract
© Yu et al. We recently developed expansion microscopy (ExM), which achieves nanoscale-precise imaging of specimens at ~70 nm resolution (with ~4.5x linear expansion) by isotropic swelling of chemically processed, hydrogel-embedded tissue. ExM of C. elegans is challenged by its cuticle, which is stiff and impermeable to antibodies. Here we present a strategy, expansion of C. elegans (ExCel), to expand fixed, intact C. elegans. ExCel enables simultaneous readout of fluorescent proteins, RNA, DNA location, and anatomical structures at resolutions of ~65–75 nm (3.3–3.8x linear expansion). We also developed epitope-preserving ExCel, which enables imaging of endogenous proteins stained by antibodies, and iterative ExCel, which enables imaging of fluorescent proteins after 20x linear expansion. We demonstrate the utility of the ExCel toolbox for mapping synaptic proteins, for identifying previously unreported proteins at cell junctions, and for gene expression analysis in multiple individual neurons of the same animal.
Date issued
2020Department
Massachusetts Institute of Technology. Department of Biological Engineering; Massachusetts Institute of Technology. Media Laboratory; McGovern Institute for Brain Research at MIT; Harvard University--MIT Division of Health Sciences and Technology; Koch Institute for Integrative Cancer Research at MIT; Massachusetts Institute of Technology. Department of Brain and Cognitive SciencesJournal
eLife
Publisher
eLife Sciences Publications, Ltd