Expansion microscopy of C. elegans

Chih-Chieh Yu(McGovern Institute for Brain Research), Nicholas C. Barry(McGovern Institute for Brain Research), Asmamaw T. Wassie(McGovern Institute for Brain Research), Anubhav Sinha(McGovern Institute for Brain Research), Abhishek Bhattacharya(Howard Hughes Medical Institute), Shoh Asano(Pfizer (United States)), Chi Zhang(McGovern Institute for Brain Research), Fei Chen(Broad Institute), Oliver Hobert(Howard Hughes Medical Institute), Miriam B. Goodman(Stanford University), Gal Haspel(Rutgers, The State University of New Jersey), Edward S. Boyden(McGovern Institute for Brain Research)
eLife
May 1, 2020
Cited by 102Open Access
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Abstract

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.


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