Mechanical expansion microscopy.

Anti-photobleaching Bacteria Cell wall Immunofluorescence Interpenetrating polymer networks Mechanically locked expansion microscopy Mechanically resolved expansion microscopy Nervous system Planarian flatworm Super-resolution fluorescence imaging

Journal

Methods in cell biology
ISSN: 0091-679X
Titre abrégé: Methods Cell Biol
Pays: United States
ID NLM: 0373334

Informations de publication

Date de publication:
2021
Historique:
entrez: 22 1 2021
pubmed: 23 1 2021
medline: 26 11 2021
Statut: ppublish

Résumé

This chapter describes two mechanical expansion microscopy methods with accompanying step-by-step protocols. The first method, mechanically resolved expansion microscopy, uses non-uniform expansion of partially digested samples to provide the imaging contrast that resolves local mechanical properties. Examining bacterial cell wall with this method, we are able to distinguish bacterial species in mixed populations based on their distinct cell wall rigidity and detect cell wall damage caused by various physiological and chemical perturbations. The second method is mechanically locked expansion microscopy, in which we use a mechanically stable gel network to prevent the original polyacrylate network from shrinking in ionic buffers. This method allows us to use anti-photobleaching buffers in expansion microscopy, enabling detection of novel ultra-structures under the optical diffraction limit through super-resolution single molecule localization microscopy on bacterial cells and whole-mount immunofluorescence imaging in thick animal tissues. We also discuss potential applications and assess future directions.

Identifiants

pubmed: 33478686
pii: S0091-679X(20)30102-3
doi: 10.1016/bs.mcb.2020.04.013
pii:
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

125-146

Subventions

Organisme : NIGMS NIH HHS
ID : T32 GM007276
Pays : United States
Organisme : NIGMS NIH HHS
ID : DP2 GM128185
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM092830
Pays : United States

Informations de copyright

© 2021 Elsevier Inc. All rights reserved.

Auteurs

Yuhang Fan (Y)

Department of Bioengineering, Stanford University, Stanford, CA, United States.

Youngbin Lim (Y)

Department of Bioengineering, Stanford University, Stanford, CA, United States.

Livia S Wyss (LS)

Department of Biology, Stanford University, Stanford, CA, United States.

Seongjin Park (S)

Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, United States.

Cancan Xu (C)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.

Huikang Fu (H)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.

Jingyi Fei (J)

Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, United States; Institute for Biophysical Dynamics, University of Chicago, Chicago, IL, United States.

Yi Hong (Y)

Department of Bioengineering, University of Texas at Arlington, Arlington, TX, United States.

Bo Wang (B)

Department of Bioengineering, Stanford University, Stanford, CA, United States; Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA, United States. Electronic address: wangbo@stanford.edu.

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Classifications MeSH