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A Universal Labeling Strategy for Nucleic Acids in Expansion Microscopy
Author(s) -
Gang Wen,
Marisa Vanheusden,
Volker Leen,
Taoufik Rohand,
Katy Vandereyken,
Thierry Voet,
Johan Hofkens
Publication year - 2021
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.1c05931
Subject(s) - oligonucleotide , chemistry , nucleic acid , fluorescence microscope , dna , in situ , context (archaeology) , rna , microscopy , fluorescence , in situ hybridization , nucleic acid thermodynamics , biophysics , conjugated system , combinatorial chemistry , computational biology , biochemistry , gene expression , gene , base sequence , organic chemistry , paleontology , physics , quantum mechanics , optics , biology , polymer
Expansion microscopy (ExM) enables the nanoscale imaging of ribonucleic acids (RNAs) on a conventional fluorescence microscope, providing information on the intricate patterns of gene expression at (sub)cellular resolution and within spatial context. To extend the use of such strategies, we examined a series of multivalent reagents that allow the labeling and grafting of deoxyribonucleic acid (DNA) oligonucleotide probes in a unified approach. We show that the reagents are directly compatible with third-generation in situ hybridization chain reaction RNA FISH (fluorescence in situ hybridization) techniques while displaying complete retention of the targeted transcripts. Furthermore, we validate and demonstrate that our labeling method is compatible with multicolor staining. Through oligonucleotide-conjugated antibodies, we demonstrate excellent performance in ×4 ExM and ×10 ExM, achieving a resolution of ∼50 nm in ×10 ExM for both pre- and postexpansion labeling strategies. Our results indicate that our multivalent molecules enable the rapid functionalization of DNA oligonucleotides for ExM.

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