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Iterative expansion microscopy.
Chang, Jae-Byum; Chen, Fei; Yoon, Young-Gyu; Jung, Erica E; Babcock, Hazen; Kang, Jeong Seuk; Asano, Shoh; Suk, Ho-Jun; Pak, Nikita; Tillberg, Paul W; Wassie, Asmamaw T; Cai, Dawen; Boyden, Edward S.
Afiliación
  • Chang JB; Media Lab, Massachusetts Institute of Technology (MIT), Cambridge, Massachusetts, USA.
  • Chen F; Department of Biomedical Engineering, Sungkyunkwan University, Suwon, Korea.
  • Yoon YG; Department of Biological Engineering, MIT, Cambridge, Massachusetts, USA.
  • Jung EE; Media Lab, Massachusetts Institute of Technology (MIT), Cambridge, Massachusetts, USA.
  • Babcock H; Department of Electrical Engineering and Computer Science, MIT, Cambridge, Massachusetts, USA.
  • Kang JS; Media Lab, Massachusetts Institute of Technology (MIT), Cambridge, Massachusetts, USA.
  • Asano S; Harvard Center for Advanced Imaging, Harvard University, Cambridge, Massachusetts, USA.
  • Suk HJ; John A. Paulson School of Engineering and Applied Sciences, Harvard University, Cambridge, Massachusetts, USA.
  • Pak N; Media Lab, Massachusetts Institute of Technology (MIT), Cambridge, Massachusetts, USA.
  • Tillberg PW; Harvard-MIT Division of Health Sciences and Technology, MIT, Cambridge, Massachusetts, USA.
  • Wassie AT; Department of Mechanical Engineering, MIT, Cambridge, Massachusetts, USA.
  • Cai D; Department of Electrical Engineering and Computer Science, MIT, Cambridge, Massachusetts, USA.
  • Boyden ES; Department of Biological Engineering, MIT, Cambridge, Massachusetts, USA.
Nat Methods ; 14(6): 593-599, 2017 Jun.
Article en En | MEDLINE | ID: mdl-28417997
ABSTRACT
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.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polímeros / Manejo de Especímenes / Aumento de la Imagen / Micromanipulación / Microscopía Tipo de estudio: Diagnostic_studies / Evaluation_studies Idioma: En Revista: Nat Methods Asunto de la revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Polímeros / Manejo de Especímenes / Aumento de la Imagen / Micromanipulación / Microscopía Tipo de estudio: Diagnostic_studies / Evaluation_studies Idioma: En Revista: Nat Methods Asunto de la revista: TECNICAS E PROCEDIMENTOS DE LABORATORIO Año: 2017 Tipo del documento: Article País de afiliación: Estados Unidos