Cargando…
X10 expansion microscopy enables 25‐nm resolution on conventional microscopes
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. Thi...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123658/ https://www.ncbi.nlm.nih.gov/pubmed/29987134 http://dx.doi.org/10.15252/embr.201845836 |
_version_ | 1783352884799209472 |
---|---|
author | Truckenbrodt, Sven Maidorn, Manuel Crzan, Dagmar Wildhagen, Hanna Kabatas, Selda Rizzoli, Silvio O |
author_facet | Truckenbrodt, Sven Maidorn, Manuel Crzan, Dagmar Wildhagen, Hanna Kabatas, Selda Rizzoli, Silvio O |
author_sort | Truckenbrodt, Sven |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-6123658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61236582018-09-10 X10 expansion microscopy enables 25‐nm resolution on conventional microscopes Truckenbrodt, Sven Maidorn, Manuel Crzan, Dagmar Wildhagen, Hanna Kabatas, Selda Rizzoli, Silvio O EMBO Rep Scientific Reports 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. John Wiley and Sons Inc. 2018-07-10 2018-09 /pmc/articles/PMC6123658/ /pubmed/29987134 http://dx.doi.org/10.15252/embr.201845836 Text en © 2018 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Scientific Reports Truckenbrodt, Sven Maidorn, Manuel Crzan, Dagmar Wildhagen, Hanna Kabatas, Selda Rizzoli, Silvio O X10 expansion microscopy enables 25‐nm resolution on conventional microscopes |
title | X10 expansion microscopy enables 25‐nm resolution on conventional microscopes |
title_full | X10 expansion microscopy enables 25‐nm resolution on conventional microscopes |
title_fullStr | X10 expansion microscopy enables 25‐nm resolution on conventional microscopes |
title_full_unstemmed | X10 expansion microscopy enables 25‐nm resolution on conventional microscopes |
title_short | X10 expansion microscopy enables 25‐nm resolution on conventional microscopes |
title_sort | x10 expansion microscopy enables 25‐nm resolution on conventional microscopes |
topic | Scientific Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6123658/ https://www.ncbi.nlm.nih.gov/pubmed/29987134 http://dx.doi.org/10.15252/embr.201845836 |
work_keys_str_mv | AT truckenbrodtsven x10expansionmicroscopyenables25nmresolutiononconventionalmicroscopes AT maidornmanuel x10expansionmicroscopyenables25nmresolutiononconventionalmicroscopes AT crzandagmar x10expansionmicroscopyenables25nmresolutiononconventionalmicroscopes AT wildhagenhanna x10expansionmicroscopyenables25nmresolutiononconventionalmicroscopes AT kabatasselda x10expansionmicroscopyenables25nmresolutiononconventionalmicroscopes AT rizzolisilvioo x10expansionmicroscopyenables25nmresolutiononconventionalmicroscopes |