Expansion microscopy of C. elegans

Author:

Yu Chih-Chieh (Jay)123ORCID,Barry Nicholas C23,Wassie Asmamaw T13,Sinha Anubhav234,Bhattacharya Abhishek5,Asano Shoh2,Zhang Chi23,Chen Fei6,Hobert Oliver5ORCID,Goodman Miriam B7ORCID,Haspel Gal89ORCID,Boyden Edward S1231011ORCID

Affiliation:

1. Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, United States

2. Media Lab, Massachusetts Institute of Technology, Cambridge, United States

3. McGovern Institute, Massachusetts Institute of Technology, Cambridge, United States

4. Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, United States

5. Department of Biological Sciences, Howard Hughes Medical Institute, Columbia University, New York, United States

6. Broad Institute of MIT and Harvard, Cambridge, United States

7. Department of Molecular and Cellular Physiology, Stanford University, Stanford, United States

8. Federated Department of Biological Sciences, New Jersey Institute of Technology and Rutgers University-Newark, Newark, United States

9. The Brain Research Institute, New Jersey Institute of Technology, Newark, United States

10. Koch Institute, Massachusetts Institute of Technology, Cambridge, United States

11. Department of Brain and Cognitive Sciences, Massachusetts Institute of Technology, Cambridge, United States

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.

Funder

McGovern Institute for Brain Research at MIT

New Jersey Institute of Technology

John Doerr

The Open Philanthropy Project

National Institutes of Health

National Science Foundation

Howard Hughes Medical Institute

U.S. Army Research Laboratory

Intelligence Advanced Research Projects Activity

Lisa Yang

Army Research Office

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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