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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Presented here is a new version of expansion microscopy (ExM), Magnify, that is modified for up to 11-fold expansion, conserving a comprehensive array of biomolecule classes, and is compatible with a broad range of tissue types. It enables the interrogation of the nanoscale configuration of biomolecules using conventional diffraction-limited microscopes.

Abstract

The nanoscale imaging of biological specimens can improve the understanding of disease pathogenesis. In recent years, expansion microscopy (ExM) has been demonstrated to be an effective and low-cost alternative to optical super-resolution microscopy. However, it has been limited by the need for specific and often custom anchoring agents to retain different biomolecule classes within the gel and by difficulties with expanding standard clinical sample formats, such as formalin-fixed paraffin-embedded tissue, especially if larger expansion factors or preserved protein epitopes are desired. Here, we describe Magnify, a new ExM method for robust expansion up to 11-fold in a wide array of tissue types. By using methacrolein as the chemical anchor between the tissue and gel, Magnify retains multiple biomolecules, such as proteins, lipids, and nucleic acids, within the gel, thus allowing the broad nanoscale imaging of tissues on conventional optical microscopes. This protocol describes best practices to ensure robust and crack-free tissue expansion, as well as tips for handling and imaging highly expanded gels.

Introduction

Biological systems exhibit structural heterogeneity, from the limbs and the organs down to the levels of proteins at the nanoscale. Therefore, a complete understanding of the operation of these systems requires visual examination across these size scales. However, the diffraction limit of light causes challenges in visualizing structures smaller than ~200-300 nm on a conventional fluorescence microscope. In addition, optical super-resolution methods1,2,3, such as stimulated emission depletion (STED), photo-activated localization microscopy (PALM), stochastic optical reco....

Protocol

All the experimental procedures involving animals were conducted in accordance with the National Institutes of Health (NIH) guidelines and were approved by the Institutional Animal Care and Use Committee at Carnegie Mellon University. Human tissue samples were commercially obtained.

1. Preparation of the stock reagents and solutions

NOTE: Refer to the Table of Materials for a list of the reagents used.

  1. Prepare the gellin.......

Representative Results

If the protocol has been successfully completed (Figure 1), the sample will appear clear and flat after heat denaturation; any folding or wrinkling indicates incomplete homogenization. A successfully expanded sample will be 3-4.5-fold larger than before expansion in 1x PBS and 8-11-fold larger when fully expanded in ddH2O. Figure 3 shows example pre- and post-expansion images of 5 µm thick FFPE human kidney sample processed using this protocol an.......

Discussion

Here, we present the Magnify protocol17, an ExM variant that can retain multiple biomolecules with a single chemical anchor and expand challenging FFPE clinical specimens up to 11-fold with heat denaturation. The key changes in this protocol that distinguish it from other ExM protocols include the use of a reformulated gel that remains mechanically robust even when fully expanded, as well as the use of methacrolein as the biomolecule anchor. The most critical steps in this protocol are as follows:.......

Acknowledgements

This work was supported by Carnegie Mellon University and the D.S.F. Charitable Foundation (Y.Z. and X.R.), the National Institutes of Health (N.I.H.) Director's New Innovator Award DP2 OD025926-01, and the Kauffman Foundation.

....

Materials

NameCompanyCatalog NumberComments
4-hydroxy-TEMPO (4HT)Sigma Aldrich176141Inhibitor
6-well glass-bottom plate (#1.5 coverglass)CellvisP06-1.5H-N
AcrylamideSigma AldrichA8887Gel Monomer component
Ammonium persulfate (APS) Sigma AldrichA3678Initiatior
DAPI (1 mg/mL)Thermo Scientific62248
Decaethylene glycol mono dodecyl ether (C12E10)Sigma AldrichP9769Non-ionic surfactant
Diamond knife No. 88 CMGeneral Tools31116
EthanolPharmco111000200
EthanolPharmco111000200
Ethylenediaminetetraacetic
acid (EDTA) 0.5 M
VWRBDH7830-1Homogenization Buffer Component
Forceps
GlycineSigma AldrichG8898Homogenization Buffer Component
HeparinSigma AldrichH3393
MethacroleinSigma Aldrich133035Anchoring Agent
Micro cover Glass #1 (24x60mm)VWR48393 106
Micro cover Glass #1.5 (24x60mm)VWR48393 251
N,N,N′,N′-
Tetramethylethylenediamine (TEMED)
Sigma AldrichT9281Accelerator
N,N′-Methylenebisacrylamide (Bis)Sigma AldrichM7279Gel Monomer component
N,N-dimethylacrylamide (DMAA)Sigma Aldrich274135Gel Monomer component
Nunclon 4-Well x 5 mL MultiDish Cell Culture DishThermo Fisher167063
Nunclon 6-Well Cell Culture DishThermo Fisher140675
Nunc™ 15mL ConicalThermo Fisher339651
Nunc™ 50mL ConicalThermo Fisher339653
Orbital Shaker
Paint brush
pH Meter
Phosphate Buffered Saline (PBS), 10x SolutionFischer ScientificBP399-1
Polyethylene glycol  200Sigma AldrichP-3015
Proteinase K (Molecular Biology Grade)Thermo ScientificEO0491
Razor bladeFischer Scientifc12640
Safelock Microcentrifuge Tubes 1.5 mLThermo Fisher3457
Safelock Microcentrifuge Tubes 2.0 mLThermo Fisher3459
Sodium acrylate (SA)AK ScientificR624Gel Monomer component
Sodium azideSigma AldrichS2002
Sodium chlorideSigma AldrichS6191
Sodium citrate tribasic dihydrateSigma AldrichC8532-1KG
Sodium dodecyl sulfate (SDS)Sigma AldrichL3771Homogenization Buffer Component
Tris BaseFischer ScientificBP152-1Homogenization Buffer Component
Triton X-100Sigma AldrichT8787
UreaSigma AldrichU5378Homogenization Buffer Component
XylenesSigma Aldrich214736
20x SSCThermo ScientificAM9763
Tween20Sigma AldrichP1379
poly-L-lysine Sigma AldrichP8920

References

  1. Hell, S. W. Far-field optical nanoscopy. Science. 316 (5828), 1153-1158 (2007).
  2. Combs, C. A., Shroff, H. Fluorescence microscopy: A concise guide to current imaging methods. Current Protocols in Neuroscience. 79

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Expansion MicroscopySuper resolution MicroscopyNanoscale ImagingBiomolecule VisualizationClinical SamplesTissue AnalysisDisease InvestigationCost effective ImagingMagnifyProtein Epitope Preservation

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