Optical imaging. Expansion microscopy.

Optical imaging. Expansion microscopy.
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光学成像。膨胀显微镜。

DOI:
10.1126/science.1260088
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发表时间:
2015-01-30
期刊:
Science (New York, N.Y.)
影响因子:
--
通讯作者:
Boyden ES
Boyden ES
中科院分区:
其他
文献类型:
--
作者:
Chen F;Tillberg PW;Boyden ES

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在光学显微镜中,精细的结构细节是通过折射来放大样品的图像来分辨的。在这里,我们报告了一项发现,通过在样品中合成一个可膨胀的聚合物网络,它可以在物理上膨胀,从而产生物理放大。通过共价将位于样品内的特定标记直接锚定到聚合物网络上,间隔比光学衍射极限更近的标记可以各向同性地分离和光学解析,这一过程我们称为膨胀显微镜(EXM)。因此,该工艺可用于使用衍射限制显微镜进行可缩放的超分辨率显微镜。我们在培养细胞和脑组织中展示了有效的~70 nm横向分辨率的exm,用传统的共聚焦显微镜对小鼠海马区~107nm3的μ进行了三色超分辨率成像。
In optical microscopy, fine structural details are resolved by using refraction to magnify images of a specimen. Here we report the discovery that, by synthesizing a swellable polymer network within a specimen, it can be physically expanded, resulting in physical magnification. By covalently anchoring specific labels located within the specimen directly to the polymer network, labels spaced closer than the optical diffraction limit can be isotropically separated and optically resolved, a process we call expansion microscopy (ExM). Thus, this process can be used to perform scalable super-resolution microscopy with diffraction-limited microscopes. We demonstrate ExM with effective ~70 nm lateral resolution in both cultured cells and brain tissue, performing three-color super-resolution imaging of ~107 μm3 of the mouse hippocampus with a conventional confocal microscope.
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