Label-retention expansion microscopy

Author:

Shi Xiaoyu12ORCID,Li Qi13ORCID,Dai Zhipeng4,Tran Arthur A.5,Feng Siyu6,Ramirez Alejandro D.1,Lin Zixi1,Wang Xiaomeng1,Chow Tracy T.7,Chen Jiapei8,Kumar Dhivya7ORCID,McColloch Andrew R.2ORCID,Reiter Jeremy F.379ORCID,Huang Eric J.8ORCID,Seiple Ian B.13,Huang Bo179ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA

2. Department of Developmental and Cell Biology, University of California, Irvine, Irvine, CA

3. Cardiovascular Research Institute, University of California, San Francisco, San Francisco, CA

4. Department of Bioengineering and Therapeutic Sciences, University of California, San Francisco, San Francisco, CA

5. Graduate Program in Chemistry and Chemical Biology, University of California, San Francisco, San Francisco, CA

6. University of California, Berkeley–University of California, San Francisco Joint Graduate Program in Bioengineering, University of California, San Francisco, San Francisco, CA

7. Department of Biochemistry and Biophysics, University of California, San Francisco, San Francisco, CA

8. Department of Pathology, University of California, San Francisco, San Francisco, CA

9. Chan Zuckerberg Biohub, San Francisco, CA

Abstract

Expansion microscopy (ExM) increases the effective resolving power of any microscope by expanding the sample with swellable hydrogel. Since its invention, ExM has been successfully applied to a wide range of cell, tissue, and animal samples. Still, fluorescence signal loss during polymerization and digestion limits molecular-scale imaging using ExM. Here, we report the development of label-retention ExM (LR-ExM) with a set of trifunctional anchors that not only prevent signal loss but also enable high-efficiency labeling using SNAP and CLIP tags. We have demonstrated multicolor LR-ExM for a variety of subcellular structures. Combining LR-ExM with superresolution stochastic optical reconstruction microscopy (STORM), we have achieved molecular resolution in the visualization of polyhedral lattice of clathrin-coated pits in situ.

Funder

National Institutes of Health

University of California, San Francisco

American Heart Association

National Science Foundation

David and Lucile Packard Foundation

Damon Runyon Cancer Research Foundation

Chan Zuckerberg

Publisher

Rockefeller University Press

Subject

Cell Biology

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