4.7 Article

Label-retention expansion microscopy

期刊

JOURNAL OF CELL BIOLOGY
卷 220, 期 9, 页码 -

出版社

ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.202105067

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资金

  1. National Institutes of Health [DP2OD008479, R01GM124334]
  2. University of California, San Francisco Mary Anne Koda-Kimble Seed Award for Innovation
  3. American Heart Association [19PRE3480616]
  4. National Science Foundation [1650113]
  5. David and Lucile Packard Foundation
  6. Damon Runyon Cancer Research Foundation [DRG2168-13]
  7. NIH Pathway to Independence Award [K99GM126136/R00GM126136]

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LR-ExM, by utilizing trifunctional anchors to prevent signal loss and enable efficient labeling, has been successfully applied to multicolor imaging of various subcellular structures.
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.

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