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Expansion microscopy of C. elegans.
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.
Affiliation
  • Yu CJ; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, United States.
  • Barry NC; Media Lab, Massachusetts Institute of Technology, Cambridge, United States.
  • Wassie AT; McGovern Institute, Massachusetts Institute of Technology, Cambridge, United States.
  • Sinha A; Media Lab, Massachusetts Institute of Technology, Cambridge, United States.
  • Bhattacharya A; McGovern Institute, Massachusetts Institute of Technology, Cambridge, United States.
  • Asano S; Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, United States.
  • Zhang C; McGovern Institute, Massachusetts Institute of Technology, Cambridge, United States.
  • Chen F; Media Lab, Massachusetts Institute of Technology, Cambridge, United States.
  • Hobert O; McGovern Institute, Massachusetts Institute of Technology, Cambridge, United States.
  • Goodman MB; Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, United States.
  • Haspel G; Department of Biological Sciences, Howard Hughes Medical Institute, Columbia University, New York, United States.
  • Boyden ES; Media Lab, Massachusetts Institute of Technology, Cambridge, United States.
Elife ; 92020 05 01.
Article in En | MEDLINE | ID: mdl-32356725
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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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caenorhabditis elegans / Caenorhabditis elegans Proteins / Microscopy, Fluorescence Limits: Animals Language: En Journal: Elife Year: 2020 Document type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Caenorhabditis elegans / Caenorhabditis elegans Proteins / Microscopy, Fluorescence Limits: Animals Language: En Journal: Elife Year: 2020 Document type: Article Affiliation country: United States