Expansion microscopy: enabling single cell analysis in intact biological systems

被引:23
作者
Alon, Shahar [1 ,2 ]
Huynh, Grace H. [1 ,2 ,3 ]
Boyden, Edward S. [1 ,2 ,4 ,5 ,6 ]
机构
[1] MIT, Media Lab, Cambridge, MA 02139 USA
[2] MIT, McGovern Inst, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[3] Microsoft Res, Seattle, WA USA
[4] MIT, Dept Biol Engn, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[5] MIT, Dept Brain & Cognit Sci, E25-618, Cambridge, MA 02139 USA
[6] MIT, Koch Inst, 77 Massachusetts Ave, Cambridge, MA 02139 USA
关键词
expansion microscopy; FISH; genomics; morphology; multiplexing; single cell analysis; super-resolution microscopy; TISSUE; REVEALS; RNA; EXPRESSION; PROTEINS; POLYACRYLAMIDE; RECONSTRUCTION; ORGANIZATION; DYNAMICS; NEURONS;
D O I
10.1111/febs.14597
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
There is a need for single cell analysis methods that enable the identification and localization of different kinds of biomolecules throughout cells and intact tissues, thereby allowing characterization and classification of individual cells and their relationships to each other within intact systems. Expansion microscopy (ExM) is a technology that physically magnifies tissues in an isotropic way, thereby achieving super-resolution microscopy on diffraction-limited microscopes, enabling rapid image acquisition and large field of view. As a result, ExM is well-positioned to integrate molecular content and cellular morphology, with the spatial precision sufficient to resolve individual biological building blocks, and the scale and accessibility required to deploy over extended 3-D objects like tissues and organs.
引用
收藏
页码:1482 / 1494
页数:13
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