| dc.contributor.author | Chang, Jae-Byum | |
| dc.contributor.author | Chen, Fei | |
| dc.contributor.author | Yoon, Young-Gyu | |
| dc.contributor.author | Jung, Erica E | |
| dc.contributor.author | Babcock, Hazen | |
| dc.contributor.author | Kang, Jeong Seuk | |
| dc.contributor.author | Asano, Shoh | |
| dc.contributor.author | Suk, Ho-Jun | |
| dc.contributor.author | Pak, Nikita | |
| dc.contributor.author | Tillberg, Paul W | |
| dc.contributor.author | Wassie, Asmamaw T | |
| dc.contributor.author | Cai, Dawen | |
| dc.contributor.author | Boyden, Edward S | |
| dc.date.accessioned | 2021-10-27T20:29:04Z | |
| dc.date.available | 2021-10-27T20:29:04Z | |
| dc.date.issued | 2017 | |
| dc.identifier.uri | https://hdl.handle.net/1721.1/135740 | |
| dc.description.abstract | © 2017 Nature America, Inc. All rights reserved. We recently developed a method called expansion microscopy, in which preserved biological specimens are physically magnified by embedding them in a densely crosslinked polyelectrolyte gel, anchoring key labels or biomolecules to the gel, mechanically homogenizing the specimen, and then swelling the gel-specimen composite by ∼4.5× in linear dimension. Here we describe iterative expansion microscopy (iExM), in which a sample is expanded ∼20×. After preliminary expansion a second swellable polymer mesh is formed in the space newly opened up by the first expansion, and the sample is expanded again. iExM expands biological specimens ∼4.5 × 4.5, or ∼20×, and enables ∼25-nm-resolution imaging of cells and tissues on conventional microscopes. We used iExM to visualize synaptic proteins, as well as the detailed architecture of dendritic spines, in mouse brain circuitry. | |
| dc.language.iso | en | |
| dc.publisher | Springer Nature | |
| dc.relation.isversionof | 10.1038/NMETH.4261 | |
| dc.rights | Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. | |
| dc.source | PMC | |
| dc.title | Iterative expansion microscopy | |
| dc.type | Article | |
| dc.contributor.department | Massachusetts Institute of Technology. Media Laboratory | |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Biological Engineering | |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Electrical Engineering and Computer Science | |
| dc.contributor.department | Harvard University--MIT Division of Health Sciences and Technology | |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Mechanical Engineering | |
| dc.contributor.department | McGovern Institute for Brain Research at MIT | |
| dc.contributor.department | Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences | |
| dc.relation.journal | Nature Methods | |
| dc.eprint.version | Author's final manuscript | |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| eprint.status | http://purl.org/eprint/status/PeerReviewed | |
| dc.date.updated | 2019-07-19T13:23:05Z | |
| dspace.orderedauthors | Chang, J-B; Chen, F; Yoon, Y-G; Jung, EE; Babcock, H; Kang, JS; Asano, S; Suk, H-J; Pak, N; Tillberg, PW; Wassie, AT; Cai, D; Boyden, ES | |
| dspace.date.submission | 2019-07-19T13:23:07Z | |
| mit.journal.volume | 14 | |
| mit.journal.issue | 6 | |
| mit.metadata.status | Authority Work and Publication Information Needed | |