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1.
Sci Rep ; 13(1): 5366, 2023 04 01.
Article in English | MEDLINE | ID: mdl-37005431

ABSTRACT

Expansion microscopy (ExM) improves imaging quality by physically enlarging the biological specimens. In principle, combining a large expansion factor with optical super-resolution should provide extremely high imaging precision. However, large expansion factors imply that the expanded specimens are dim and are therefore poorly suited for optical super-resolution. To solve this problem, we present a protocol that ensures the expansion of the samples up to 10-fold, in a single expansion step, through high-temperature homogenization (X10ht). The resulting gels exhibit a higher fluorescence intensity than gels homogenized using enzymatic digestion (based on proteinase K). This enables the sample analysis by multicolor stimulated emission depletion (STED) microscopy, for a final resolution of 6-8 nm in neuronal cell cultures or isolated vesicles. X10ht also enables the expansion of 100-200 µm thick brain samples, up to 6-fold. The better epitope preservation also enables the use of nanobodies as labeling probes and the implementation of post-expansion signal amplification. We conclude that X10ht is a promising tool for nanoscale resolution in biological samples.


Subject(s)
Hot Temperature , Neurons , Microscopy, Fluorescence/methods , Brain , Gels
2.
EMBO Rep ; 19(9)2018 09.
Article in English | MEDLINE | ID: mdl-29987134

ABSTRACT

Expansion microscopy is a recently introduced imaging technique that achieves super-resolution through physically expanding the specimen by ~4×, after embedding into a swellable gel. The resolution attained is, correspondingly, approximately fourfold better than the diffraction limit, or ~70 nm. This is a major improvement over conventional microscopy, but still lags behind modern STED or STORM setups, whose resolution can reach 20-30 nm. We addressed this issue here by introducing an improved gel recipe that enables an expansion factor of ~10× in each dimension, which corresponds to an expansion of the sample volume by more than 1,000-fold. Our protocol, which we termed X10 microscopy, achieves a resolution of 25-30 nm on conventional epifluorescence microscopes. X10 provides multi-color images similar or even superior to those produced with more challenging methods, such as STED, STORM, and iterative expansion microscopy (iExM). X10 is therefore the cheapest and easiest option for high-quality super-resolution imaging currently available. X10 should be usable in any laboratory, irrespective of the machinery owned or of the technical knowledge.


Subject(s)
Microscopy, Fluorescence/methods , Acrylamide/chemistry , Animals , Cell Line , Cerebellum/ultrastructure , Chlorocebus aethiops , Ethylenediamines/chemistry , Hydrogel, Polyethylene Glycol Dimethacrylate/chemistry , Neurons/ultrastructure , Peroxisomes/ultrastructure , Polymerization , Potassium Compounds/chemistry , Rats , Rats, Wistar , Sulfates/chemistry , Synapses/ultrastructure , Tubulin/ultrastructure
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