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Expansion microscopy of C. elegans

Authors :
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 Sciences
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
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 Sciences
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
Source :
eLife
Publication Year :
2021

Abstract

© 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.

Details

Database :
OAIster
Journal :
eLife
Notes :
application/pdf, English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1286401896
Document Type :
Electronic Resource