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Nanoscale Imaging of RNA with Expansion Microscopy

The ability to image RNA identity and location with nanoscale precision in intact tissues is of great interest for defining cell types and states in normal and pathological biological settings. Here, we present a strategy for expansion microscopy (ExM) of RNA. We developed a small molecule linker th...

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Detalles Bibliográficos
Autores principales: Chen, Fei, Wassie, Asmamaw T., Cote, Allison J., Sinha, Anubhav, Alon, Shahar, Asano, Shoh, Daugharthy, Evan R., Chang, Jae-Byum, Marblestone, Adam, Church, George M., Raj, Arjun, Boyden, Edward S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965288/
https://www.ncbi.nlm.nih.gov/pubmed/27376770
http://dx.doi.org/10.1038/nmeth.3899
Descripción
Sumario:The ability to image RNA identity and location with nanoscale precision in intact tissues is of great interest for defining cell types and states in normal and pathological biological settings. Here, we present a strategy for expansion microscopy (ExM) of RNA. We developed a small molecule linker that enables RNA to be covalently attached to a swellable polyelectrolyte gel synthesized throughout a biological specimen. Then, post-expansion, fluorescent in situ hybridization (FISH) imaging of RNA can be performed with high yield and specificity, with single molecule precision, in both cultured cells and intact brain tissue. Expansion FISH (ExFISH) de-crowds RNAs and supports amplification of single molecule signals (i.e., via hybridization chain reaction (HCR)) as well as multiplexed RNA FISH readout. ExFISH thus enables super-resolution imaging of RNA structure and location with diffraction-limited microscopes in thick specimens, such as intact brain tissue and other tissues of importance to biology and medicine.